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<title>American Journal of Neuroradiology</title>
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<link>http://www.ajnr.org</link>
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<title><![CDATA[[LETTERS] CT Angiography is State-of-the-Art First Vascular Imaging for Subarachnoid Hemorrhage]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e41?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Fox, A.J., Symons, S.P., Aviv, R.I.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1049</dc:identifier>
<dc:title><![CDATA[[LETTERS] CT Angiography is State-of-the-Art First Vascular Imaging for Subarachnoid Hemorrhage]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e42</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e41</prism:startingPage>
<prism:section>LETTERS</prism:section>
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<title><![CDATA[[LETTERS] Death by Nondiagnosis: Why Emergent CT Angiography Should Not Be Done for Patients with Subarachnoid Hemorrhage]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e43?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Westerlaan, H.E., Eshghi, S., Oudkerk, M., Groen, R.J.M., Metzemaekers, J.D.M., van Dijk, J.M.C., Mooij, J.J.A.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1011</dc:identifier>
<dc:title><![CDATA[[LETTERS] Death by Nondiagnosis: Why Emergent CT Angiography Should Not Be Done for Patients with Subarachnoid Hemorrhage]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e43</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e43</prism:startingPage>
<prism:section>LETTERS</prism:section>
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<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e44?rss=1">
<title><![CDATA[[LETTERS] Regarding the Risk of Death from CT Angiography in Patients with Subarachnoid Hemorrhage]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e44?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Livingston, R. R.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0954</dc:identifier>
<dc:title><![CDATA[[LETTERS] Regarding the Risk of Death from CT Angiography in Patients with Subarachnoid Hemorrhage]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e44</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e44</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e45?rss=1">
<title><![CDATA[[LETTERS] Life at the End of the Tunnel: Why Emergent CT Angiography Should Be Done for Patients With Acute Subarachnoid Hemorrhage]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e45?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Agid, R., Willinsky, R.A., Farb, R.I., Terbrugge, K.G.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1014</dc:identifier>
<dc:title><![CDATA[[LETTERS] Life at the End of the Tunnel: Why Emergent CT Angiography Should Be Done for Patients With Acute Subarachnoid Hemorrhage]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e45</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e45</prism:startingPage>
<prism:section>LETTERS</prism:section>
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<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e46?rss=1">
<title><![CDATA[[LETTERS] Reply:]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e46?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Kallmes, D. F., Layton, K. F., Marx, W. F., Tong, F.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1047</dc:identifier>
<dc:title><![CDATA[[LETTERS] Reply:]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e47</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e46</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e48?rss=1">
<title><![CDATA[[BOOK REVIEWS] Carotid Disease: The Role of Imaging in Diagnosis and Management]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e48?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0979</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Carotid Disease: The Role of Imaging in Diagnosis and Management]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e49</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e48</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e50?rss=1">
<title><![CDATA[[BOOK REVIEWS] MRI From Picture to Proton: 2nd ed.]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e50?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0980</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] MRI From Picture to Proton: 2nd ed.]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e50</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e50</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e51?rss=1">
<title><![CDATA[[BOOK REVIEWS] Atlas of Neurosurgical Techniques, 2-Vol. Set]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e51?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0981</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Atlas of Neurosurgical Techniques, 2-Vol. Set]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e52</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e51</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e53?rss=1">
<title><![CDATA[[BOOK REVIEWS] Pediatric Neuropathology: A Text-Atlas]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e53?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0982</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Pediatric Neuropathology: A Text-Atlas]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e53</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e53</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/e54?rss=1">
<title><![CDATA[[BOOK REVIEWS] BOOKS RECEIVED]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/e54?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:title><![CDATA[[BOOK REVIEWS] BOOKS RECEIVED]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e54</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>e54</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1035?rss=1">
<title><![CDATA[[EDITORIALS] Cross-Checking for Plagiarism]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1035?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Castillo, M., Halm, K.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1178</dc:identifier>
<dc:title><![CDATA[[EDITORIALS] Cross-Checking for Plagiarism]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1035</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1035</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1036?rss=1">
<title><![CDATA[[REVIEW ARTICLES] Posterior Reversible Encephalopathy Syndrome, Part 1: Fundamental Imaging and Clinical Features]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1036?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Posterior reversible encephalopathy syndrome (PRES) is a neurotoxic state coupled with a unique CT or MR imaging appearance. Recognized in the setting of a number of complex conditions (preeclampsia/eclampsia, allogeneic bone marrow transplantation, organ transplantation, autoimmune disease and high dose chemotherapy) the imaging, clinical and laboratory features of this toxic state are becoming better elucidated. This review summarizes the basic and advanced imaging features of PRES, along with pertinent features of the clinical and laboratory presentation and available histopathology. Many common imaging/clinical/laboratory observations are present among these patients, despite the perception of widely different associated clinical conditions.</P>
]]></description>
<dc:creator><![CDATA[Bartynski, W.S.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0928</dc:identifier>
<dc:title><![CDATA[[REVIEW ARTICLES] Posterior Reversible Encephalopathy Syndrome, Part 1: Fundamental Imaging and Clinical Features]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1042</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1036</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1043?rss=1">
<title><![CDATA[[REVIEW ARTICLES] Posterior Reversible Encephalopathy Syndrome, Part 2: Controversies Surrounding Pathophysiology of Vasogenic Edema]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1043?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Posterior reversible encephalopathy syndrome (PRES) is a neurotoxic state accompanied by a unique brain imaging pattern typically associated with a number of complex clinical conditions including: preeclampsia/eclampsia, allogeneic bone marrow transplantation, solid organ transplantation, autoimmune diseases and high dose cancer chemotherapy. The mechanism behind the developing vasogenic edema and CT or MR imaging appearance of PRES is not known. Two theories have historically been proposed: 1) Severe hypertension leads to failed auto-regulation, subsequent hyperperfusion, with endothelial injury/vasogenic edema and; 2) vasoconstriction and hypoperfusion leads to brain ischemia and subsequent vasogenic edema. The strengths/weaknesses of these hypotheses are reviewed in a translational fashion including supporting evidence and current available imaging/clinical data related to the conditions that develop PRES. While the hypertension/hyperperfusion theory has been most popular, the conditions associated with PRES have a similar immune challenge present and develop a similar state of T-cell/endothelial cell activation that may be the basis of leukocyte trafficking and systemic/cerebral vasoconstriction. These systemic features along with current vascular and perfusion imaging features in PRES appear to render strong support for the older theory of vasoconstriction coupled with hypoperfusion as the mechanism.</P>
]]></description>
<dc:creator><![CDATA[Bartynski, W.S.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0929</dc:identifier>
<dc:title><![CDATA[[REVIEW ARTICLES] Posterior Reversible Encephalopathy Syndrome, Part 2: Controversies Surrounding Pathophysiology of Vasogenic Edema]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1049</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1043</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1050?rss=1">
<title><![CDATA[[INTERVENTIONAL] Recurrent Intracranial Stenosis Induced by the Wingspan Stent: Comparison with Balloon Angioplasty Alone in a Single Patient]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1050?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We present a case in which angioplasty alone and stent-assisted angioplasty were performed in the same patient to treat medically refractory intracranial stenoses. This elderly patient with presumed intracranial atherosclerotic disease underwent angioplasty alone for his anterior cerebral artery stenosis. Stent-assisted angioplasty was used for treatment of his ipsilateral middle cerebral artery stenosis. Follow-up angiography at 4 months documented severe recurrent stenosis confined only to the stented portion of the middle cerebral artery.</P>
]]></description>
<dc:creator><![CDATA[Layton, K.F., Hise, J.H., Thacker, I.C.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1006</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Recurrent Intracranial Stenosis Induced by the Wingspan Stent: Comparison with Balloon Angioplasty Alone in a Single Patient]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1052</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1050</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1053?rss=1">
<title><![CDATA[[INTERVENTIONAL] Intra-Arterial Nimodipine for Severe Cerebral Vasospasm after Aneurysmal Subarachnoid Hemorrhage: Influence on Clinical Course and Cerebral Perfusion]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1053?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> The efficacy of intra-arterial administration of nimodipine (IAN) in patients with severe vasospasm after aneurysmal subarachnoid hemorrhage (SAH) remains unproved. The goal of the present study was to investigate the clinical effect and cerebral perfusion after IAN in patients with severe vasospasm refractory to hemodynamic treatment.</P>
<P><B>MATERIALS AND METHODS:</B> Twenty-six of 214 patients with aneurysmal SAH were included in the prospective study, approved by the local ethics committee. All patients met the criteria of medically refractory cerebral vasospasm. Effectiveness was monitored angiographically by digital subtraction angiography and by transcranial Doppler (TCD), perfusion CT (PCT), and neurologic examination during treatment course and follow-up.</P>
<P><B>RESULTS:</B> No angiographic effect was observed in 8 patients. The pooled PCT values revealed a reduction of time to peak (<I>P</I> = .03) and mean transit time (<I>P</I> = .17) 1 day after intervention. This effect did not persist during the following days. The pooled TCD analysis demonstrated a transient increase in flow 1 day after intervention (<I>P</I> = .03). No trend was evident during the next 7 days after intervention. Additional infarction was experienced by 61.1% of patients.</P>
<P><B>CONCLUSIONS:</B> IAN in a selective patient group resulted in a positive response with reduction of angiographic vasospasm and increase in cerebral perfusion as detected by PCT after 24 hours. Therefore, IAN appears more effective than intra-arterial papaverine. Nevertheless the efficacy of IAN is temporary. Therefore, the search for more effective treatment strategies to reduce critical vasospasm and to improve cerebral perfusion must be continued.</P>
]]></description>
<dc:creator><![CDATA[Hanggi, D., Turowski, B., Beseoglu, K., Yong, M., Steiger, H.J.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1005</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Intra-Arterial Nimodipine for Severe Cerebral Vasospasm after Aneurysmal Subarachnoid Hemorrhage: Influence on Clinical Course and Cerebral Perfusion]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1060</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1053</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1061?rss=1">
<title><![CDATA[[INTERVENTIONAL] Simultaneous Treatment with Intravenous Recombinant Tissue Plasminogen Activator and Endovascular Therapy for Acute Ischemic Stroke Within 3 Hours of Onset]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1061?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Because intravenous (IV) recombinant tissue plasminogen activator (rtPA) does not always lead to a good outcome in a considerable proportion of patients, combined IV rtPA and rescue endovascular therapy (ET) have been performed in several recent studies. However, rescue therapy after completion of IV rtPA often results in late ineffective recanalization. We examined the efficacy and safety of combined IV rtPA and simultaneous ET as primary rather than rescue therapy for hyperacute middle cerebral artery (MCA) occlusion.</P>
<P><B>MATERIALS AND METHODS:</B> A total of 29 patients eligible for IV rtPA, who were diagnosed as having MCA (M1 or M2) occlusion within 3 hours of onset, underwent thrombolysis. In the combined group, patients were treated by IV rtPA (0.6 mg/kg for 60 minutes) and simultaneous ET (intra-arterial rtPA, mechanical thrombus disruption with microguidewire, and balloon angioplasty) initiated as soon as possible. In the IV group, patients were treated by IV rtPA only.</P>
<P><B>RESULTS:</B> The improvement of the National Institutes of Health Stroke Scale (NIHSS) score at 24 hours was 11 &plusmn; 4.8 in the combined group versus 5 &plusmn; 4.3 in the IV group (<I>P</I> &lt; .001). In the combined group, successful recanalization was observed in 14 (88%) of 16 patients with no symptomatic intracranial hemorrhage, and 10 (63%) of 16 patients had favorable outcomes (modified Rankin Scale [mRS] 0, 1) at 3 months.</P>
<P><B>CONCLUSIONS:</B> Aggressive combined therapy with IV rtPA and simultaneous ET markedly improved the clinical outcome of hyperacute MCA occlusion without significant adverse effect. Additional randomized study is needed to confirm our results.</P>
]]></description>
<dc:creator><![CDATA[Sugiura, S., Iwaisako, K., Toyota, S., Takimoto, H.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1012</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Simultaneous Treatment with Intravenous Recombinant Tissue Plasminogen Activator and Endovascular Therapy for Acute Ischemic Stroke Within 3 Hours of Onset]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1066</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1061</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1067?rss=1">
<title><![CDATA[[INTERVENTIONAL] Interval Change in Size of Venous Pouch Canine Bifurcation Aneurysms over a 10-Month Period]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1067?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> The natural history study of experimental aneurysms is important for the evaluation of new endovascular occlusion devices. Our purpose was to evaluate the natural history of experimental venous pouch bifurcation aneurysms in mongrel dogs up to a 10-month period.</P>
<P><B>MATERIALS AND METHODS:</B> Serial digital subtraction angiography was performed in 5 bifurcation aneurysms 1, 4, 7, and 10 months after surgical creation. Aneurysm dimensions, including height, width, and neck diameter, and animal body weights were measured. Comparisons of each parameter were performed using the Friedman test and the paired Wilcoxon signed-rank test.</P>
<P><B>RESULTS:</B> Four of 5 aneurysms were patent during a 10-month follow-up period. One aneurysm was regarded as a partially thrombosed aneurysm at 1 month, though the extent of partial thrombosis lessened at 10 months. Bifurcation aneurysms progressively increased in size (aneurysm height, width, and neck diameter) during the first several months.</P>
<P><B>CONCLUSION:</B> If this experimental model is used to evaluate new endovascular devices for cerebral aneurysm treatment, investigators should be aware of early progressive aneurysm enlargement.</P>
]]></description>
<dc:creator><![CDATA[Tsumoto, T., Song, J.K., Niimi, Y., Berenstein, A.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1046</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Interval Change in Size of Venous Pouch Canine Bifurcation Aneurysms over a 10-Month Period]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1070</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1067</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1071?rss=1">
<title><![CDATA[[INTERVENTIONAL] Subtraction 3D CT Angiography with the Orbital Synchronized Helical Scan Technique for the Evaluation of Postoperative Cerebral Aneurysms Treated with Cobalt-Alloy Clips]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1071?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> CT angiography (CTA) has been used for the evaluation of intracranial aneurysms and recently has been applied to assess postoperative aneurysms treated with titanium-alloy clips. We investigated the clinical usefulness of subtraction CTA by using the orbital synchronized helical scan technique (OSHST) for evaluating intracranial aneurysms surgically treated with cobalt-alloy clips.</P>
<P><B>MATERIALS AND METHODS:</B> We scanned an agar gel phantom with a cobalt-alloy clip mounted in the center by using subtraction CT with and without OSHST. Eighteen patients (20 aneurysms) who underwent surgery with cobalt-alloy clips were postoperatively evaluated with subtraction CTA with OSHST, and the results were compared with those from digital subtraction angiography. Two neuroradiologists independently evaluated the 3D CTA images and source images with and without subtraction for the presence of residual flow in the aneurysm and stenotic change in parent or neighboring arteries.</P>
<P><B>RESULTS:</B> For the phantom study, significantly fewer artifacts from clips were noted on images obtained by using subtraction CT with OSHST than on those obtained without OSHST. For the clinical study, subtraction CTA with OSHST also showed fewer clip artifacts than did conventional CTA. Image quality was poor, and we were unable to diagnose residual neck for 5% (1/20) with subtraction CTA with OSHST and 75% (15/20) with conventional CTA. For evaluation of adjacent vessels, image quality was poor for none (0/20) with subtraction CTA with OSHST and for 55% (11/20) with conventional CTA. For subtraction CTA with OSHST, sensitivity in detecting residual neck was 1.0, and specificity was 0.94. For conventional CTA, sensitivity and specificity were both 0.25.</P>
<P><B>CONCLUSIONS:</B> OSHST is a useful technique for subtracting cobalt-alloy clips, and subtraction CTA with OSHST is available for evaluating aneurysms after clipping with cobalt-alloy clips.</P>
]]></description>
<dc:creator><![CDATA[Watanabe, Y., Kashiwagi, N., Yamada, N., Higashi, M., Fukuda, T., Morikawa, S., Onishi, Y., Iihara, K., Miyamoto, S., Naito, H.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1040</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Subtraction 3D CT Angiography with the Orbital Synchronized Helical Scan Technique for the Evaluation of Postoperative Cerebral Aneurysms Treated with Cobalt-Alloy Clips]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1075</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1071</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1076?rss=1">
<title><![CDATA[[INTERVENTIONAL] Patient Skin Dose during Neuroembolization by Multiple-Point Measurement Using a Radiosensitive Indicator]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1076?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Although neuroembolization has recently spread quickly, sufficient attention has not been focused on the associated radiation exposure. The purpose of this research was to evaluate the patient's entrance skin dose (ESD) during neuroembolizations in 6 institutions.</P>
<P><B>MATERIALS AND METHODS:</B> This study was approved by all of the 6 institutional review boards, and all of the patients gave informed consent. This study included a total of 103 consecutive neuroembolizations in the 6 institutions. Patient ESDs during the procedures were evaluated by using caps that had 44 radiosensitive indicators adherent to the surface. The patient ESDs were calculated from the color difference of the indicators. To check for effects on the scalp, clinical follow-up was performed at 1-2 days, 2 weeks, and 3 months after the procedure.</P>
<P><B>RESULTS:</B> The averages of total fluoroscopic time, total number of digital subtraction angiography frames, and dose area product were 67.1 &plusmn; 41.6 minutes, 883 &plusmn; 626, and 257 &plusmn; 150 Gy <FONT FACE="arial,helvetica">x</FONT> cm<SUP>2</SUP>, respectively. The average maximum ESD for each patient was 1.9 &plusmn; 1.1 Gy (range, 0.4&ndash;5.6 Gy; median, 1.5 Gy). The average maximum ESDs of each institution ranged from 1.0 to 2.4 Gy. Epilation was observed in 6 patients.</P>
<P><B>CONCLUSIONS:</B> The maximum ESDs during neuroembolizations exceed the thresholds for radiation skin injuries in some cases.</P>
]]></description>
<dc:creator><![CDATA[Suzuki, S., Furui, S., Matsumaru, Y., Nobuyuki, S., Ebara, M., Abe, T., Itoh, D.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1045</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Patient Skin Dose during Neuroembolization by Multiple-Point Measurement Using a Radiosensitive Indicator]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1081</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1076</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1082?rss=1">
<title><![CDATA[[PEDIATRICS] Prevalence and Evolution of Intracranial Hemorrhage in Asymptomatic Term Infants]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1082?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Subdural hemorrhage (SDH) is often associated with infants experiencing nonaccidental injury (NAI). A study of the appearance and natural evolution of these birth-related hemorrhages, particularly SDH, is important in the forensic evaluation of NAI. The purpose of this study was to determine the normal incidence, size, distribution, and natural history of SDH in asymptomatic term neonates as detected by sonography (US) and MR imaging within 72 hours of birth.</P>
<P><B>MATERIALS AND METHODS:</B> Birth history, delivery method, duration of each stage of labor, pharmaceutic augmentation, and complications during delivery as well as postnatal physical examination were recorded. Brain MR imaging and US were performed on 101 asymptomatic term infants at 3&ndash;7 days, 2 weeks, 1 month, and 3 months. Clinical follow-up at 24 months was recorded.</P>
<P><B>RESULTS:</B> Forty-six neonates had SDH by MR imaging within 72 hours of delivery. SDH was seen in both vaginal and cesarean deliveries. All neonates were asymptomatic, with normal findings on physical examination. All 46 had supratentorial SDH seen in the posterior cranium. Twenty (43%) also had infratentorial SDH. US detected 11 of the 20 (55%) infratentorial SDHs and no supratentorial SDH. Most SDHs present at birth were &le;3 mm and had resolved by 1 month, and all resolved by 3 months on MR imaging. Most children with SDHs had normal findings on developmental examinations at 24 months.</P>
<P><B>CONCLUSION:</B> SDH in asymptomatic term neonates after delivery is limited in size and location.</P>
]]></description>
<dc:creator><![CDATA[Rooks, V.J., Eaton, J.P., Ruess, L., Petermann, G.W., Keck-Wherley, J., Pedersen, R.C.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1004</dc:identifier>
<dc:title><![CDATA[[PEDIATRICS] Prevalence and Evolution of Intracranial Hemorrhage in Asymptomatic Term Infants]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1089</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1082</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1090?rss=1">
<title><![CDATA[[PEDIATRICS] Prenatal and Neonatal MR Imaging Findings in Oral-Facial-Digital Syndrome Type VI]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1090?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We report prenatal and neonatal neuroimaging findings in a case of oral-facial-digital syndrome type VI (OFDS VI). Prenatal MR imaging at 29 weeks' gestation showed hypoplastic cerebellar vermis and hemispheres, the molar tooth sign, and a hypothalamic hamartoma. Neonatal MR imaging confirmed these findings. The neonate developed breathing abnormalities and exhibited frontal bossing, multiple bucco-alveolar frenula, and postaxial hexadactyly of both hands. If the molar tooth sign and a hypothalamic hamartoma are present, prenatal diagnosis of OFDS VI is possible.</P>
]]></description>
<dc:creator><![CDATA[Poretti, A., Brehmer, U., Scheer, I., Bernet, V., Boltshauser, E.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1038</dc:identifier>
<dc:title><![CDATA[[PEDIATRICS] Prenatal and Neonatal MR Imaging Findings in Oral-Facial-Digital Syndrome Type VI]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1091</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1090</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1092?rss=1">
<title><![CDATA[[SPINE] High-Resolution Diffusion-Weighted MR Imaging of the Human Lumbosacral Plexus and Its Branches Based on a Steady-State Free Precession Imaging Technique at 3T]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1092?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> 3D diffusion-weighted steady-state free precession imaging (3D DW-SSFP) with isotropic resolution was performed to delineate structures of the human lumbosacral plexus (LSP). 3D DW-SSFP clearly revealed detailed anatomy of the LSP and its branches. Our data suggest that the sequence based on 3D DW-SSFP can be used for high-resolution MR imaging of the peripheral nervous system.</P>
]]></description>
<dc:creator><![CDATA[Zhang, Z.W., Song, L.J., Meng, Q.F., Li, Z.P., Luo, B.N., Yang, Y.H., Pei, Z.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0994</dc:identifier>
<dc:title><![CDATA[[SPINE] High-Resolution Diffusion-Weighted MR Imaging of the Human Lumbosacral Plexus and Its Branches Based on a Steady-State Free Precession Imaging Technique at 3T]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1094</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1092</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1095?rss=1">
<title><![CDATA[[SPINE] Preoperative Onyx Embolization of Aggressive Vertebral Hemangiomas]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1095?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We report the first use of Onyx in the embolization of spinal tumors in 2 cases of aggressive vertebral hemangioma. In both cases, Onyx embolization provided effective preoperative tumor devascularization after the initial prolonged particulate embolization with Embospheres made little overall impact. Onyx enables a more rapid and visible embolization than particles and is less technically demanding than traditional liquid embolic agents, such as <I>n</I>-butyl cyanoacrylate.</P>
]]></description>
<dc:creator><![CDATA[Hurley, M.C., Gross, B.A., Surdell, D., Shaibani, A., Muro, K., Mitchell, C.M., Doppenberg, E.M., Bendok, B.R.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1010</dc:identifier>
<dc:title><![CDATA[[SPINE] Preoperative Onyx Embolization of Aggressive Vertebral Hemangiomas]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1097</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1095</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1098?rss=1">
<title><![CDATA[[SPINE] Effects of Diagnostic Information, Per Se, on Patient Outcomes in Acute Radiculopathy and Low Back Pain]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1098?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> We conducted a prospective randomized study of patients with acute low back pain and/or radiculopathy to assess the effect of knowledge of diagnostic findings on clinical outcome. The practice of ordering spinal imaging, perhaps unintentionally, includes a large number of patients for whom the imaging test is performed for purposes of reassurance or because of patient expectations. If this rationale is valid, one would expect to see a measurable effect from diagnostic information, per se.</P>
<P><B>MATERIALS AND METHODS:</B> A total of 246 patients with acute (&lt;3 weeks) low back pain (LBP) and/or radiculopathy (150 LBP and 96 radiculopathy patients) were recruited. Patients were randomized using a stratified block design with equal allocation to either the unblinded group (MR imaging results provided within 48 hours) or the blinded group (both patient and physician blinded to MR imaging results.) After the initial MR imaging, patients followed 6 weeks of conservative management. Roland function, visual pain analog, absenteeism, Short Form (SF)-36 Health Status Survey, self-efficacy scores, and Fear Avoidance Questionnaire were completed at presentation; 2, 4, 6, and 8 weeks; and 6, 12, and 24 months. Improvement of Roland score by 50% or more and patient satisfaction assessed by Cherkin symptom satisfaction measure were considered a positive outcome.</P>
<P><B>RESULTS:</B> Clinical outcome at 6 weeks was similar for unblinded and blinded patients. Self-efficacy, fear avoidance beliefs, and the SF-36 subscales were similar over time for blinded and unblinded patients, except for the general health subscale on the SF-36. General health of the blinded group improved more than for the unblinded group (<I>P</I> = .008).</P>
<P><B>CONCLUSIONS:</B> Patient knowledge of imaging findings do not alter outcome and are associated with a lesser sense of well-being.</P>
]]></description>
<dc:creator><![CDATA[Ash, L.M., Modic, M.T., Obuchowski, N.A., Ross, J.S., Brant-Zawadzki, M.N., Grooff, P.N.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0999</dc:identifier>
<dc:title><![CDATA[[SPINE] Effects of Diagnostic Information, Per Se, on Patient Outcomes in Acute Radiculopathy and Low Back Pain]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1103</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1098</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1104?rss=1">
<title><![CDATA[[SPINE] Unusual Manifestations of Vertebral Osteomyelitis: Intraosseous Lesions Mimicking Metastases]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1104?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Vertebral osteomyelitis can have different imaging manifestations. The purpose of this study was to demonstrate the unusual MR imaging patterns of vertebral osteomyelitis with intraosseous lesions mimicking metastases.</P>
<P><B>MATERIALS AND METHODS:</B> From September 2000 to August 2007, 7 patients were selected from our data base of 214 patients with confirmed vertebral osteomyelitis and MR images. All of those having misinterpreted MR imaging reports and unusual imaging patterns were analyzed. The presence of a peripheral curvilinear area of low signal intensity in an osseous lesion (the rim sign) and a peripheral rim of high signal intensity on T2-weighted images around an osseous lesion (the halo sign) was evaluated. Follow-up MR imaging studies were performed in all patients.</P>
<P><B>RESULTS:</B> The patients were 5 men and 2 women, with an age range of 42&ndash;80 years. MR imaging findings of those with vertebral osteomyelitis showed a solitary lesion in 2 and multiple lesions in 5 patients. The intraosseous lesions revealed low signal intensity on T1-weighted images, mixed or high signal intensity on T2-weighted images, high signal intensity on short  inversion recovery images, and global or marginal enhancement. The rim sign was found in 6 (86%) patients; halo sign, in 7 (100%); preserved intervertebral disks, in 7 (100%); and limited paraspinal or epidural inflammation, in 6 (86%). Images of all patients demonstrated healing or almost healed changes on the follow-up MR imaging studies.</P>
<P><B>CONCLUSION:</B> Vertebral osteomyelitis can have MR imaging patterns mimicking osseous metastases. Recognition of these unusual imaging manifestations, together with clinical and histopathologic analysis, may aid in reaching the correct diagnosis.</P>
]]></description>
<dc:creator><![CDATA[Hsu, C.Y., Yu, C.W., Wu, M.Z., Chen, B.B., Huang, K.M., Shih, T.T.F.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1003</dc:identifier>
<dc:title><![CDATA[[SPINE] Unusual Manifestations of Vertebral Osteomyelitis: Intraosseous Lesions Mimicking Metastases]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1110</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1104</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1111?rss=1">
<title><![CDATA[[BRAIN] An Acute Ischemic Stroke Classification Instrument That Includes CT or MR Angiography: The Boston Acute Stroke Imaging Scale]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1111?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> A simple classification instrument based on imaging that predicts outcomes in patients with actute ischemic stroke is lacking. We tested the hypotheses that the Boston Acute Stroke Imaging Scale (BASIS) classification instrument effectively predicts patient outcomes and is superior to the Alberta Stroke Program Early CT Score (ASPECTS) in predicting outcomes in acute ischemic stroke.</P>
<P><B>MATERIALS AND METHODS:</B> Of 230 prospectively screened, consecutive patients with acute ischemic stroke, 87 had noncontrast CT (NCCT)/CT angiography (CTA), and 118 had MR imaging/MR angiography (MRA) at admission and were classified as having major stroke by BASIS criteria if they had a proximal cerebral artery occlusion or, if no occlusion, imaging evidence of significant parenchymal ischemia; all of the others were classified as minor strokes. Outcomes included death, length of hospitalization, and discharge disposition. BASIS was compared with ASPECTS (dichotomized &gt; or &le;7) in 87 patients who had NCCT/CTA.</P>
<P><B>RESULTS:</B> BASIS classification by NCCT/CTA was equivalent to MR imaging/MRA. Fifty-six of 205 patients were classified as having major strokes including all 6 of the deaths. A total of 71.4% and 15.4% of major and minor stroke survivors, respectively, were discharged to a rehabilitation facility, whereas 14.3% and 79.2% of patients with major and minor strokes were discharged to home. The mean length of hospitalization was 12.3 and 3.3 days for the major and minor stroke groups, respectively (all outcomes, <I>P</I> &lt; .0001). In 87 NCCT/CTA patients, BASIS and ASPECTS agreed in 22 major and 44 minor strokes. BASIS classified 21 patients as having major strokes who were classified as having minor strokes by ASPECTS. The BASIS major/ASPECTS minor stroke group had outcomes similar to those classified as major strokes by both instruments.</P>
<P><B>CONCLUSIONS:</B> The BASIS classification instrument is effective and appears superior to ASPECTS in predicting outcomes in acute ischemic stroke.</P>
]]></description>
<dc:creator><![CDATA[Torres-Mozqueda, F., He, J., Yeh, I.B., Schwamm, L.H., Lev, M.H., Schaefer, P.W., Gonzalez, R.G.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1000</dc:identifier>
<dc:title><![CDATA[[BRAIN] An Acute Ischemic Stroke Classification Instrument That Includes CT or MR Angiography: The Boston Acute Stroke Imaging Scale]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1117</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1111</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1118?rss=1">
<title><![CDATA[[BRAIN] CT Perfusion Identifies Increased Salvage of Tissue in Patients Receiving Intravenous Recombinant Tissue Plasminogen Activator within 3 Hours of Stroke Onset]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1118?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> In spite of the advent of thrombolytic therapy, CT-perfusion imaging is currently not fully used for clinical decision-making and not included in published clinical guidelines for management of ischemic stroke. We investigated whether lesion volumes on cerebral blood volume (CBV), cerebral blood flow (CBF), and mean transit time (MTT) maps predict final infarct volume and whether all these parameters are needed for triage to intravenous recombinant tissue plasminogen activator (rtPA). We also investigated the effect of intravenous rtPA on affected brain by measuring salvaged tissue volume in patients receiving intravenous rtPA and in controls.</P>
<P><B>MATERIALS AND METHODS:</B> Forty-four patients receiving intravenous rtPA and 19 controls underwent CT perfusion (CTP) studies in the emergency department within 3 hours of stroke onset. Lesion volumes were measured on MTT, CBV, and CBF maps by region-of-interest analysis and were compared with follow-up CT volumes by correlation and regression analysis. The volume of salvaged tissue was determined as the difference between the initial MTT and follow-up CT lesion volumes and was compared between intravenous rtPA-treated patients and controls.</P>
<P><B>RESULTS:</B> No significant difference between the groups was observed in lesion volume assessed from the CTP maps (<I>P</I> &gt; .08). Coefficients of determination for MTT, CBF, and CBV versus follow-up CT lesion volumes were 0.3, 0.3, 0.47, with intravenous rtPA; and 0.53, 0.55, and 0.81 without intravenous rtPA. Regression of MTT on CBF lesion volumes showed codependence (<I>R</I><SUP>2</SUP> = 0.98, <I>P</I> &lt; .0001). Mean salvaged tissue volumes with intravenous rtPA were 21.8 &plusmn; 17.1 and 13.2 &plusmn; 13.5 mL in controls; these were significantly different by using nonparametric (<I>P</I> &lt; .03) and Fisher exact tests (<I>P</I> &lt; .04).</P>
<P><B>CONCLUSIONS:</B> Within 3 hours of stroke onset, CBV lesion volume does not necessarily represent dead tissue. MTT lesion volume alone can be used to identify the upper limit of the size of abnormally perfused brain. More brain is salvaged in patients with intravenous rtPA than in controls.</P>
]]></description>
<dc:creator><![CDATA[Silvennoinen, H.M., Hamberg, L.M., Lindsberg, P.J., Valanne, L., Hunter, G.J.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1039</dc:identifier>
<dc:title><![CDATA[[BRAIN] CT Perfusion Identifies Increased Salvage of Tissue in Patients Receiving Intravenous Recombinant Tissue Plasminogen Activator within 3 Hours of Stroke Onset]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1123</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1118</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1124?rss=1">
<title><![CDATA[[BRAIN] Regional Differences in Diffusion Tensor Imaging Measurements: Assessment of Intrarater and Interrater Variability]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1124?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Diffusion tensor imaging (DTI) has become a valuable tool in both the research and clinical evaluation of subjects. We sought to quantify interobserver and intraobserver variability of diffusivity and diffusion anisotropy measurements with regard to specific regions of interest (ROIs).</P>
<P><B>MATERIALS AND METHODS:</B> The subject group consisted of 5 healthy control subjects and 7 study subjects (all males; 16&ndash;19 years old; mean age = 17.5 years), as part of a protocol for closed head injury. Two whole-brain DTI scans were acquired on a 3T scanner for each subject. Analysis was performed using a ROI approach. Two independent observers analyzed the apparent diffusion coefficient (ADC) and fractional anisotropy (FA) indices in the corpus callosum, cortical spinal tract, internal capsules (ICs), basal ganglia, and centrum semiovale (CSO). Intraobserver and interobserver variability were calculated for the mean ADC, FA, and ordered eigenvalues of the diffusion tensor (<SUB>1</SUB>, <SUB>2</SUB>, and <SUB>3</SUB>).</P>
<P><B>RESULTS:</B> The overall  statistic for intraobserver variability for both observers showed slight-to-substantial agreement ( = 0.02&ndash;0.69), however FA values in the CSO showed only slight agreement. Interobserver agreement was also slight to substantial for these DTI measurements with high variability in FA values in the IC and CSO.</P>
<P><B>CONCLUSIONS:</B> When one is comparing 2 DTI measurements, it is important to assess intraobserver and interobserver variability. We recommend caution in the analysis of DTI contrasts in the IC and CSO, because we have found the widest range of variability in measurements within these structures.</P>
]]></description>
<dc:creator><![CDATA[Ozturk, A., Sasson, A.D., Farrell, J.A.D., Landman, B.A., da Motta, A.C.B.S., Aralasmak, A., Yousem, D.M.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0998</dc:identifier>
<dc:title><![CDATA[[BRAIN] Regional Differences in Diffusion Tensor Imaging Measurements: Assessment of Intrarater and Interrater Variability]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1127</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1124</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1128?rss=1">
<title><![CDATA[[BRAIN] Reproducibility, Interrater Agreement, and Age-Related Changes of Fractional Anisotropy Measures at 3T in Healthy Subjects: Effect of the Applied b-Value]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1128?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> There is no reproducibility study of fractional anisotropy (FA) measurements at 3T using regions of interest (ROIs). Our purpose was to establish the extent and statistical significance of the interrater variability, the variability observed with 2 different b-values, and in 2 separate scanning sessions.</P>
<P><B>MATERIALS AND METHODS:</B> Twelve healthy volunteers underwent MR imaging twice. MR imaging was performed on a 3T unit, and FA maps were analyzed independently by 2 observers using ROIs positioned in the corpus callosum, internal capsules, corticospinal tracts, and right thalamus. Changes in FA values (<FONT FACE="arial,helvetica">x</FONT>10<SUP>3</SUP>) measured with 2 b-values (700 and 1000 s/mm<SUP>2</SUP>), age-related differences, interobserver agreement, and measurement reproducibility were assessed.</P>
<P><B>RESULTS:</B> In the right internal capsule genu (FA = 702/728; <I>b</I> = 1000/700 s/mm<SUP>2</SUP>) and the left anterior limb of the internal capsule (AIC; FA = 617/745; <I>b</I> = 1000/700 s/mm<SUP>2</SUP>), the FA values were significantly different between the 2 b-values (<I>P</I> = .02 and .05, respectively). Significant age-related differences in FA were observed in the genu of the corpus callosum and in the left AIC. Interrater measurements showed fair-to-moderate agreement for most anatomic structures. The lowest significant change for a single subject regarding any FA values between the 2 sessions was in the corpus callosum (4%), whereas the highest one was in the corticospinal tracts (27%). The Bland-Altman plot analysis showed that the 1000-s/mm<SUP>2</SUP> b-value gave satisfactorily reproducible measurements equally good or better than the 700-s/mm<SUP>2</SUP> b-value.</P>
<P><B>CONCLUSION:</B> The reproducibility of FA estimates using ROIs was satisfactory. Measurements with a b-value at 1000 s/mm<SUP>2</SUP> showed superior reproducibility in most anatomic locations.</P>
]]></description>
<dc:creator><![CDATA[Bisdas, S., Bohning, D.E., Besenski, N., Nicholas, J.S., Rumboldt, Z.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1044</dc:identifier>
<dc:title><![CDATA[[BRAIN] Reproducibility, Interrater Agreement, and Age-Related Changes of Fractional Anisotropy Measures at 3T in Healthy Subjects: Effect of the Applied b-Value]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1133</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1128</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1134?rss=1">
<title><![CDATA[[BRAIN] Tract-Based Spatial Statistics of Diffusion Tensor Imaging in Adults with Dyslexia]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1134?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Diffusion tensor imaging is a tool that can be used to study white matter microstructure in dyslexia. We tested the hypothesis that dyslexics have a white matter structural change (as measured by directional diffusion of water, which can be affected by disruption in white matter tracts) between brain regions that previous functional connectivity studies showed were associated with phonologic processing.</P>
<P><B>MATERIALS AND METHODS:</B> Diffusion tensor imaging (DTI) scans were acquired from 7 healthy adult normal readers and from 14 adults with dyslexia on a 1.5T scanner. Voxelwise statistical analysis of the fractional anisotropy data were carried out by using Tract-Based Spatial Statistics to compare dyslexic subjects versus control subjects in white matter tracts.</P>
<P><B>RESULTS:</B> Significant group difference map clusters (comparing adults with and without dyslexia) occurred in specific bilateral white matter tracts within the frontal lobe, temporal lobe, occipital lobe, and parietal lobe.</P>
<P><B>CONCLUSION:</B> The DTI fractional anisotropy results in the bilateral white matter showing higher fractional anisotropy in adult control subjects compared with adults with dyslexia (relating to white matter fiber tract integrity) are consistent with our previous functional connectivity results from seed points in the bilateral inferior frontal gyrus.</P>
]]></description>
<dc:creator><![CDATA[Richards, T., Stevenson, J., Crouch, J., Johnson, L.C., Maravilla, K., Stock, P., Abbott, R., Berninger, V.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1007</dc:identifier>
<dc:title><![CDATA[[BRAIN] Tract-Based Spatial Statistics of Diffusion Tensor Imaging in Adults with Dyslexia]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1139</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1134</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1140?rss=1">
<title><![CDATA[[BRAIN] Inclusion or Exclusion of Intratumoral Vessels in Relative Cerebral Blood Volume Characterization in Low-Grade Gliomas: Does It Make a Difference?]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1140?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We assessed the influence of inclusion (method 1) and exclusion (method 2) of intratumoral vessels when determining maximum relative cerebral blood volume (rCBVmax) in 3 types of low-grade gliomas (LGGs): astrocytomas, oligoastrocytomas, and oligodendrogliomas. Method 1 yielded significantly higher mean rCBVmax than method 2. However, only method 2 demonstrated a significant (<I>P</I> = .026) association between rCBVmax and membership of a differently ranked histologic category. Exclusion of intratumoral vessels appears, therefore, preferable when determining rCBVmax in LGGs.</P>
]]></description>
<dc:creator><![CDATA[Caseiras, G. B., Thornton, J.S., Yousry, T., Benton, C., Rees, J., Waldman, A.D., Jager, H.R.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0993</dc:identifier>
<dc:title><![CDATA[[BRAIN] Inclusion or Exclusion of Intratumoral Vessels in Relative Cerebral Blood Volume Characterization in Low-Grade Gliomas: Does It Make a Difference?]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1141</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1140</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1142?rss=1">
<title><![CDATA[[BRAIN] Cerebral Corticospinal Tract Injury Resulting from High-Voltage Electrical Shock]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1142?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Electrical injuries are becoming more common and are increasingly imaged with advanced technologies, such as MR imaging. However, the MR imaging findings of such injuries remain largely unstudied. We report a high-voltage electrical injury to the cerebral corticospinal tracts and document evolution on serial MR images.</P>
]]></description>
<dc:creator><![CDATA[Johansen, C.K., Welker, K.M., Lindell, E.P., Petty, G.W.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1009</dc:identifier>
<dc:title><![CDATA[[BRAIN] Cerebral Corticospinal Tract Injury Resulting from High-Voltage Electrical Shock]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1143</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1142</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1144?rss=1">
<title><![CDATA[[BRAIN] Eye Position Information on CT Increases the Identification of Acute Ischemic Hypoattenuation]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1144?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> It is possible that identification of eye deviation may sensitize a scan reader to early brain hypodensity associated with an arterial occlusive process. Our aim was to investigate the value of observing eye deviation on blinded CT identification of early hypoattenuation following ischemic infarct.</P>
<P><B>MATERIALS AND METHODS:</B> Two staff and 2 fellow neuroradiologists reviewed 75 brain CT scans obtained within 3 hours of acute ischemia from subjects in the Interventional Management of Stroke Study. Films were reviewed 3 months apart, the first time with tape over the eyes on the images, the second with the eyes visible. Readers were asked if early hypoattenuation in the middle cerebral artery (MCA) distribution or if a hyperattenuated MCA was present.  statistics were calculated to determine agreement among the 4 readers and between each of the 2 readings by the same reader, not only for the original interpretation of the blinded study neuroradiologist but also for the Alberta Stroke Program Early CT Score (ASPECTS) for each subject assigned by an unblinded expert panel. A generalized estimating equations modeling approach was used to look at the overall effect of including eye information for agreement between interpretations.</P>
<P><B>RESULTS:</B> Eye information availability was associated with improved agreement for detection of early ischemic hypoattenuation not only among the 4 readers but also between the 4 readers and both the blinded study neuroradiologist (<I>P</I> = .02) and the unblinded expert ASPECTS panel. When comparing first and second readings for hypoattenuation, we also noted increased mean values for sensitivity (46.8% first, 56.5% second), specificity (78.2%, 80.2%), positive predictive value (72.0%, 80.7%), negative predictive value (55.5%, 61.0%), and percentage agreement (61.0%, 67.5%).</P>
<P><B>CONCLUSION:</B> Observation of CT eye deviation significantly improves reader identification of acute ischemic hypoattenuation.</P>
]]></description>
<dc:creator><![CDATA[Mahajan, V., Minshew, P.T., Khoury, J., Shu, P.P., Muzaffar, M., Abruzzo, T., Leach, J.L., Tomsick, T.A.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0995</dc:identifier>
<dc:title><![CDATA[[BRAIN] Eye Position Information on CT Increases the Identification of Acute Ischemic Hypoattenuation]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1146</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1144</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1147?rss=1">
<title><![CDATA[[BRAIN] Diffusion-Weighted MR Imaging: Diagnosing Atypical or Malignant Meningiomas and Detecting Tumor Dedifferentiation]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1147?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Atypical and malignant meningiomas are uncommon tumors with aggressive behavior and higher mortality, morbidity, and recurrence compared with benign tumors. We investigated the utility of diffusion-weighted (DW) MR imaging to differentiate atypical/malignant from benign meningiomas and to detect histologic dedifferentiation to higher tumor grade.</P>
<P><B>MATERIALS AND METHODS:</B> We retrospectively compared conventional and DW MR images (b-value 1000 s/mm<SUP>2</SUP>) acquired on a 1.5T clinical scanner between 25 atypical/malignant and 23 benign meningiomas. The optimal cutoff for the absolute apparent diffusion coefficient (ADC) and normalized ADC (NADC) ratio to differentiate between the groups was determined by using receiver operating characteristic (ROC) analysis.</P>
<P><B>RESULTS:</B> Irregular tumor margins, peritumoral edema, and adjacent bone destruction occurred significantly more often in atypical/malignant than in benign meningiomas. The mean ADC of atypical/malignant meningiomas (0.66 &plusmn; 0.13 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP>/s) was significantly lower compared with benign meningiomas (0.88 &plusmn; 0.08 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP>/s; <I>P</I> &lt; .0001). Mean NADC ratio in the atypical/malignant group (0.91 &plusmn; 0.18) was also significantly lower than the benign group (1.28 &plusmn; 0.11; <I>P</I> &lt; .0001), without overlap between groups. ROC analysis showed that ADC and NADC thresholds of 0.80 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP>/s and 0.99, respectively, had the best accuracy: at the NADC threshold of 0.99, the sensitivity and specificity were 96% and 100%, respectively. Two patients had isointense benign tumors on initial DW MR imaging, and these became hyperintense with the decrease in ADC and NADC below these thresholds when they progressed to atypical and malignant meningiomas on recurrence.</P>
<P><B>CONCLUSIONS:</B> ADC and NADC ratios in atypical/malignant meningiomas are significantly lower than in benign tumors. Decrease in ADC and NADC on follow-up imaging may suggest dedifferentiation to higher tumor grade.</P>
]]></description>
<dc:creator><![CDATA[Nagar, V.A., Ye, J.R., Ng, W.H., Chan, Y.H., Hui, F., Lee, C.K., Lim, C.C.T.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0996</dc:identifier>
<dc:title><![CDATA[[BRAIN] Diffusion-Weighted MR Imaging: Diagnosing Atypical or Malignant Meningiomas and Detecting Tumor Dedifferentiation]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1152</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1147</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1153?rss=1">
<title><![CDATA[[BRAIN] Performance Evaluation of Radiologists with Artificial Neural Network for Differential Diagnosis of Intra-Axial Cerebral Tumors on MR Images]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1153?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Previous studies have suggested that use of an artificial neural network (ANN) system is beneficial for radiological diagnosis. Our purposes in this study were to construct an ANN for the differential diagnosis of intra-axial cerebral tumors on MR images and to evaluate the effect of ANN outputs on radiologists' diagnostic performance.</P>
<P><B>MATERIALS AND METHODS:</B> We collected MR images of 126 patients with intra-axial cerebral tumors (58 high-grade gliomas, 37 low-grade gliomas, 19 metastatic tumors, and 12 malignant lymphomas). We constructed a single 3-layer feed-forward ANN with a Levenberg-Marquardt algorithm. The ANN was designed to differentiate among 4 categories of tumors (high-grade gliomas, low-grade gliomas, metastases, and malignant lymphomas) with use of 2 clinical parameters and 13 radiologic findings in MR images. Subjective ratings for the 13 radiologic findings were provided independently by 2 attending radiologists. All 126 cases were used for training and testing of the ANN based on a leave-one-out-by-case method. In the observer test, MR images were viewed by 9 radiologists, first without and then with ANN outputs. Each radiologist's performance was evaluated through a receiver operating characteristic (ROC) analysis on a continuous rating scale.</P>
<P><B>RESULTS:</B> The averaged area under the ROC curve for ANN alone was 0.949. The diagnostic performance of the 9 radiologists increased from 0.899 to 0.946 (<I>P</I> &lt; .001) when they used ANN outputs.</P>
<P><B>CONCLUSIONS:</B> The ANN can provide useful output as a second opinion to improve radiologists' diagnostic performance in the differential diagnosis of intra-axial cerebral tumors seen on MR imaging.</P>
]]></description>
<dc:creator><![CDATA[Yamashita, K., Yoshiura, T., Arimura, H., Mihara, F., Noguchi, T., Hiwatashi, A., Togao, O., Yamashita, Y., Shono, T., Kumazawa, S., Higashida, Y., Honda, H.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1037</dc:identifier>
<dc:title><![CDATA[[BRAIN] Performance Evaluation of Radiologists with Artificial Neural Network for Differential Diagnosis of Intra-Axial Cerebral Tumors on MR Images]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1158</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1153</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1159?rss=1">
<title><![CDATA[[BRAIN] Diffusion Tensor Imaging in Chronic Subdural Hematoma: Correlation between Clinical Signs and Fractional Anisotropy in the Pyramidal Tract]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1159?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Diffusion tensor imaging (DTI) was introduced as a good technique to evaluate structural abnormalities in the white matter. In this study, we used DTI to examine anisotropic changes of the pyramidal tracts displaced by chronic subdural hematoma (CSDH).</P>
<P><B>MATERIALS AND METHODS:</B> Twenty-six patients with unilateral CSDH underwent DTI before and after surgery. We measured fractional anisotropy (FA) values in pyramidal tracts of bilateral cerebral peduncles and calculated the ratio of the FA value on the lesion side to that on the contralateral side (FA ratio) and compared the ratios with motor weakness. Moreover, the relationships between FA ratios and clinical factors such as age, sex, midline shift, interval from trauma, and hematoma attenuation on CT were evaluated.</P>
<P><B>RESULTS:</B> FA values of pyramidal tracts on the lesion side were significantly lower than those on the contralateral side (0.66 &plusmn; 0.07 versus 0.74 &plusmn; 0.05, <I>P</I> &lt; .0001). The FA ratio was correlated to the severity of motor weakness (<I>r</I><SUP>2</SUP> = 0.32, <I>P</I> = .002). FA ratios after surgery improved significantly compared with those before surgery (0.96 &plusmn; 0.08 versus 0.89 &plusmn; 0.07, <I>P</I> = .0004). Intervals from trauma and the midline shift were significantly associated with decreased FA ratios (<I>P</I> = .0008 and <I>P</I> = .037).</P>
<P><B>CONCLUSIONS:</B> In patients with CSDH, a reversible decrease of FA in the affected pyramidal tract on DTI was correlated to motor weakness. These anisotropic changes were considered to be caused by a reversible distortion of neuron fibers and vasogenic edema due to the hematoma.</P>
]]></description>
<dc:creator><![CDATA[Yokoyama, K., Matsuki, M., Shimano, H., Sumioka, S., Ikenaga, T., Hanabusa, K., Yasuda, S., Inoue, H., Watanabe, T., Miyashita, M., Hiramatsu, R., Murao, K., Kondo, A., Tanabe, H., Kuroiwa, T.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1001</dc:identifier>
<dc:title><![CDATA[[BRAIN] Diffusion Tensor Imaging in Chronic Subdural Hematoma: Correlation between Clinical Signs and Fractional Anisotropy in the Pyramidal Tract]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1163</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1159</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1164?rss=1">
<title><![CDATA[[BRAIN] Diffuse Pachymeningeal Hyperintensity and Subdural Effusion/Hematoma Detected by Fluid-Attenuated Inversion Recovery MR Imaging in Patients with Spontaneous Intracranial Hypotension]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1164?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Fluid-attenuated inversion recovery (FLAIR) MR imaging has advantages to detect meningeal lesions. FLAIR MR imaging was used to detect pachymeningeal thickening and thin bilateral subdural effusion/hematomas in patients with spontaneous intracranial hypotension (SIH).</P>
<P><B>MATERIALS AND METHODS:</B> Eight patients were treated under clinical diagnoses of SIH. Chronologic MR imaging studies, including the FLAIR sequence, were retrospectively reviewed.</P>
<P><B>RESULTS:</B> Initial MR imaging showed diffuse pachymeningeal thickening as isointense in 6 cases, hypoisointense in 1 case, and isohyperintense in 1 case on the T1-weighted MR images, and hyperintense in all cases on both T2-weighted and FLAIR MR images. Dural (pachymeningeal) hyperintensity on FLAIR MR imaging had the highest contrast to CSF, and was observed as linear in all patients, usually located in the supratentorial convexity and also parallel to the falx, the dura of the posterior fossa convexity, and the tentorium, and improved after treatment. These characteristics of diffuse pachymeningeal hyperintensity on FLAIR MR imaging were similar to diffuse pachymeningeal enhancement (DPME) on T1-weighted imaging with gadolinium. Initial FLAIR imaging clearly showed subdural effusion/hematomas in 6 of 8 patients. The thickness of subdural effusion/hematomas sometimes increased transiently after successful treatment and resolution of clinical symptoms.</P>
<P><B>CONCLUSION:</B> Diffuse pachymeningeal hyperintensity on FLAIR MR imaging is a similar sign to DPME for the diagnosis of SIH but does not require injection of contrast medium. FLAIR is useful sequence for the detection of subdural effusion/hematomas in patients with SIH.</P>
]]></description>
<dc:creator><![CDATA[Tosaka, M., Sato, N., Fujimaki, H., Tanaka, Y., Kagoshima, K., Takahashi, A., Saito, N., Yoshimoto, Y.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1041</dc:identifier>
<dc:title><![CDATA[[BRAIN] Diffuse Pachymeningeal Hyperintensity and Subdural Effusion/Hematoma Detected by Fluid-Attenuated Inversion Recovery MR Imaging in Patients with Spontaneous Intracranial Hypotension]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1170</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1164</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1171?rss=1">
<title><![CDATA[[BRAIN] Signal Intensity of the Motor Cortex on Phase-Weighted Imaging at 3T]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1171?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> It is known that the motor cortex shows hypointensity on T2-weighted images in older patients. The goal of this study was to assess the signal intensity of the motor cortices on the phase-weighted imaging performed with a Windows-based software program that we developed ourselves.</P>
<P><B>MATERIALS AND METHODS:</B> All studies were performed at 3T MR imaging. First, the TE for the phase-weighted image was optimized; the best contrast between the motor and other cortices was obtained with a TE of 40 ms. The study population consisted of 45 healthy subjects (23 females, 22 males; mean age, 32.1 years). The signal intensity of the motor cortices was divided into 3 grades by 2 neuroradiologists in comparison with that of the superior frontal cortex (SFC): In grade I, the motor cortex was isointense to the SFC; in grade II, the motor cortex was slightly hypointense to the SFC; and in grade III, the motor cortex was markedly hypointense to the SFC.</P>
<P><B>RESULTS:</B> The motor cortex was classified as either grade II or III in all subjects older than 20 years of age on the phase-weighted images. Even at 10&ndash;19 years of age, the grade II or III appearance was found in 14 (88%) of 16 motor cortices (8 subjects) on the phase-weighted images.</P>
<P><B>CONCLUSION:</B> In adolescents, the motor cortex is hypointense to other cerebral cortices on phase-weighted MR imaging, which probably reflects differences in the concentration of nonheme iron and/or in the tissue architecture.</P>
]]></description>
<dc:creator><![CDATA[Kakeda, S., Korogi, Y., Kamada, K., Ohnari, N., Moriya, J., Sato, T., Kitajima, M., Hasnine, H., Hirata, N.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1002</dc:identifier>
<dc:title><![CDATA[[BRAIN] Signal Intensity of the Motor Cortex on Phase-Weighted Imaging at 3T]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1175</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1171</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1176?rss=1">
<title><![CDATA[[BRAIN] Metabolic Assessment of Gliomas Using 11C-Methionine, [18F] Fluorodeoxyglucose, and 11C-Choline Positron-Emission Tomography]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1176?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Positron-emission tomography (PET) is a useful tool in oncology. The aim of this study was to assess the metabolic activity of gliomas using <SUP>11</SUP>C-methionine (MET), [<SUP>18</SUP>F] fluorodeoxyglucose (FDG), and <SUP>11</SUP>C-choline (CHO) PET and to explore the correlation between the metabolic activity and histopathologic features.</P>
<P><B>MATERIALS AND METHODS:</B> PET examinations were performed for 95 primary gliomas (37 grade II, 37 grade III, and 21 grade IV). We measured the tumor/normal brain uptake ratio (T/N ratio) on each PET and investigated the correlations among the tracer uptake, tumor grade, tumor type, and tumor proliferation activity. In addition, we compared the ease of visual evaluation for tumor detection.</P>
<P><B>RESULTS:</B> All 3 of the tracers showed positive correlations with astrocytic tumor (AT) grades (II/IV and III/IV). The MET T/N ratio of oligodendroglial tumors (OTs) was significantly higher than that of ATs of the same grade. The CHO T/N ratio showed a significant positive correlation with histopathologic grade in OTs. Tumor grade and type influenced MET uptake only. MET T/N ratios of more than 2.0 were seen in 87% of all of the gliomas. All of the tracers showed significantly positive correlations with Mib-1 labeling index in ATs but not in OTs and oligoastrocytic tumors.</P>
<P><B>CONCLUSION:</B> MET PET appears to be useful in evaluating grade, type, and proliferative activity of ATs. CHO PET may be useful in evaluating the potential malignancy of OTs. In terms of visual evaluation of tumor localization, MET PET is superior to FDG and CHO PET in all of the gliomas, due to its straightforward detection of "hot lesions".</P>
]]></description>
<dc:creator><![CDATA[Kato, T., Shinoda, J., Nakayama, N., Miwa, K., Okumura, A., Yano, H., Yoshimura, S., Maruyama, T., Muragaki, Y., Iwama, T.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1008</dc:identifier>
<dc:title><![CDATA[[BRAIN] Metabolic Assessment of Gliomas Using 11C-Methionine, [18F] Fluorodeoxyglucose, and 11C-Choline Positron-Emission Tomography]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1182</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1176</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1183?rss=1">
<title><![CDATA[[BRAIN] Morphometric Changes in the Episodic Memory Network and Tau Pathologic Features Correlate with Memory Performance in Patients with Mild Cognitive Impairment]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1183?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Mild cognitive impairment (MCI) may affect several cognitive domains, including attention and reasoning, but is often first characterized by memory deficits. The purpose of this study was to ask these 2 questions: 1) Can levels of CSF tau proteins and amyloid beta 42 peptide explain thinning of the cerebral cortex in patients with MCI? 2) How are brain morphometry, CSF biomarkers, and apolipoprotein E (APOE) allelic variation related to episodic memory function in MCI?</P>
<P><B>MATERIALS AND METHODS:</B> Hippocampal volume and cortical thickness were estimated by MR imaging and compared for patients with MCI (<I>n</I> = 18) and healthy controls (<I>n</I> = 18). In addition, regions of interest (ROIs) were selected in areas where the MCI group had atrophy and which overlapped with the episodic memory network (temporal, entorhinal, inferior parietal, precuneus/posterior cingulate, and frontal). Relationships among morphometry, CSF biomarkers, APOE, and memory were tested. The analyses were repeated with an independent sample of patients with MCI (<I>n</I> = 19).</P>
<P><B>RESULTS:</B> Patients with MCI and pathologic CSF values had hippocampal atrophy. However, both patients with pathologic and patients with nonpathologic CSF had a thinner cortex outside the hippocampal area. CSF pathology was related to hippocampal volume, whereas relationships with cortical thickness were found mainly in one of the samples. Morphometry correlated robustly with memory performance across MCI samples, whereas less stable results were found for tau protein.</P>
<P><B>CONCLUSION:</B> The differences in hippocampal volume between the MCI and the healthy control groups were only found in patients with pathologic CSF biomarkers, whereas differences in cortical thickness were also found for patients without such pathologic features. Morphometry in areas in the episodic memory network was robustly correlated with memory performance. It is speculated that atrophy in these areas may be associated with the memory problems seen in MCI.</P>
]]></description>
<dc:creator><![CDATA[Fjell, A.M., Walhovd, K.B., Amlien, I., Bjornerud, A., Reinvang, I., Gjerstad, L., Cappelen, T., Willoch, F., Due-Tonnessen, P., Grambaite, R., Skinningsrud, A., Stenset, V., Fladby, T.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1059</dc:identifier>
<dc:title><![CDATA[[BRAIN] Morphometric Changes in the Episodic Memory Network and Tau Pathologic Features Correlate with Memory Performance in Patients with Mild Cognitive Impairment]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1189</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1183</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1190?rss=1">
<title><![CDATA[[BRAIN] Can MR Imaging Diagnose Adult-Onset Alexander Disease?]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1190?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> In recent years, the discovery that mutations in the glial fibrillary acidic protein gene (<I>GFAP</I>) were responsible for Alexander disease (AD) brought recognition of adult cases. The purpose of this study was to demonstrate that MR imaging allows identification of cases of AD with adult onset (AOAD), which are remarkably different from infantile cases.</P>
<P><B>MATERIALS AND METHODS:</B> In this retrospective study, brain and spinal cord MR imaging studies of 11 patients with AOAD (7 men, 4 women; age range, 26&ndash;64 years; mean age, 43.6 years), all but 1 genetically confirmed, were reviewed. Diffusion and spectroscopic investigations were available in 6 patients each.</P>
<P><B>RESULTS:</B> Atrophy and changes in signal intensity in the medulla oblongata and upper cervical spinal cord were present in 11 of 11 cases and were the diagnostic features of AOAD. Minimal to moderate supratentorial periventricular abnormalities were seen in 8 patients but were absent in the 3 oldest patients. In these patients, postcontrast enhancement was also absent. Mean diffusivity was not altered except in abnormal white matter (WM). Increase in myo-inositol (mIns) was also restricted to abnormal periventricular WM.</P>
<P><B>CONCLUSIONS:</B> Awareness of the MR pattern described allows an effective selection of the patients who need genetic investigations for the <I>GFAP</I> gene. This MR pattern even led to identification of asymptomatic cases and should be regarded as highly characteristic of AOAD.</P>
]]></description>
<dc:creator><![CDATA[Farina, L., Pareyson, D., Minati, L., Ceccherini, I., Chiapparini, L., Romano, S., Gambaro, P., Fancellu, R., Savoiardo, M.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1060</dc:identifier>
<dc:title><![CDATA[[BRAIN] Can MR Imaging Diagnose Adult-Onset Alexander Disease?]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1196</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1190</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1197?rss=1">
<title><![CDATA[[HEAD & NECK] [18F] Fluorodeoxyglucose Positron-Emission Tomography-CT Imaging of Carotidynia]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1197?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Carotidynia is an idiopathic syndrome characterized by pain over the carotid bifurcation without associated luminal pathologic process. The classification of carotidynia as a distinct disease rather than as a symptom has generated controversy in the literature. Recent reports, however, suggest that carotidynia is a distinct disease characterized by the presence of enhancing soft tissue in the carotid sheath. We describe findings of carotidynia on positron-emission tomography and CT that further support the classification of carotidynia as a distinct inflammatory disease.</P>
]]></description>
<dc:creator><![CDATA[Amaravadi, R.R., Behr, S.C., Kousoubris, P.D., Raja, S.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1013</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] [18F] Fluorodeoxyglucose Positron-Emission Tomography-CT Imaging of Carotidynia]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1199</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1197</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1200?rss=1">
<title><![CDATA[[HEAD & NECK] Eccentric Stenosis of the Carotid Artery Associated with Ipsilateral Cerebrovascular Events]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1200?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Eccentric stenosis of the coronary artery is associated with plaque disruption and acute coronary syndrome. The purpose of the present study was to determine whether eccentric stenosis of the carotid artery contributes to cerebrovascular events.</P>
<P><B>MATERIALS AND METHODS:</B> Of 6859 patients with vascular diseases who underwent duplex carotid ultrasonography, we studied 512 internal carotid arteries in 441 patients who had a maximum area stenosis at or more than 70%, which corresponds with approximately 50% or more by the NASCET method. The maximal (A) and minimal wall thicknesses (B) were measured on cross-sectional sonography images, and an eccentricity index was calculated using the following formula: (A &ndash; B)/A. Arteries in the lowest quartile of the eccentricity index (&lt;0.69) were defined as having a concentric stenosis, whereas the others were defined as having eccentric stenosis. The underlying clinical characteristics and plaque morphologies, as well as the occurrence of ipsilateral ischemic stroke or transient ischemic attack in the preceding year, were compared between patients with eccentric and concentric stenosis.</P>
<P><B>RESULTS:</B> Patient characteristics and plaque morphology were similar between the 2 groups. Cerebrovascular events occurred more frequently ipsilaterally to the artery with eccentric stenosis (13.5%) than to the artery with concentric stenosis (5.5%; <I>P</I> = .013); the difference was more evident when cerebrovascular events of presumed carotid arterial origin were assessed (<I>P</I> = .005). After adjusting for risk factors and plaque morphology, eccentric stenosis was independently related to the presence of recent cerebrovascular events (odds ratio = 2.76; 95% confidence interval = 1.19&ndash;6.40).</P>
<P><B>CONCLUSIONS:</B> In patients with an area carotid stenosis of 70% or more, eccentric plaque was associated with a significantly increased incidence of ipsilateral cerebrovascular events compared with patients with concentric stenosis.</P>
]]></description>
<dc:creator><![CDATA[Ohara, T., Toyoda, K., Otsubo, R., Nagatsuka, K., Kubota, Y., Yasaka, M., Naritomi, H., Minematsu, K.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A0997</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] Eccentric Stenosis of the Carotid Artery Associated with Ipsilateral Cerebrovascular Events]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1203</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1200</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1204?rss=1">
<title><![CDATA[[HEAD & NECK] Sinonasal Organized Hematoma: CT and MR Imaging Findings]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1204?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Sinonasal organized hematoma (OH) is an uncommon, nonneoplastic benign condition that can be locally aggressive. The purpose of this work was to characterize the CT and MR imaging findings of sinonasal OH.</P>
<P><B>MATERIALS AND METHODS:</B> CT (<I>n</I> = 11) and MR (<I>n</I> = 10) images of 12 patients (9 men and 3 women; mean age, 41 years; range, 12&ndash;76 years) with pathologically proved sinonasal OH were retrospectively reviewed. Particular attention was put on the location, shape, size, extent, internal architecture, and enhancement pattern of the lesion and associated sinus wall change.</P>
<P><B>RESULTS:</B> The lesions were seen as an expansile (<I>n</I> = 9) or nonexpansile (<I>n</I> = 3) mass, ranging in size from 2.2 to 6.0 cm (mean, 4.2 cm), primarily involving the maxillary sinus (<I>n</I> = 11) or nasal cavity (<I>n</I> = 1) unilaterally. The ipsilateral nasal cavity was also involved in 9 of 11 maxillary sinus lesions. Smooth sinus wall erosion other than the medial maxillary sinus wall was noted in 8 lesions. The internal architecture was best displayed on T2-weighted MR images on which all of the lesions were seen as a mixture of marked heterogeneous hypointensity and isointensity, surrounded by a hypointense peripheral rim, reflecting histologic heterogeneity of the lesion composed of hemorrhage, fibrosis, and neovascularization. Marked irregular nodular, papillary, or frondlike enhancement at the areas of neovascularization was also a typical finding seen in all of the lesions.</P>
<P><B>CONCLUSION:</B> An expansile soft tissue mass, smooth sinus wall erosion, marked heterogeneous signal intensity with a hypointense peripheral rim on T2-weighted MR images, and marked irregular nodular, papillary, or frondlike enhancement are characteristic CT and MR imaging findings of sinonasal OH.</P>
]]></description>
<dc:creator><![CDATA[Kim, E.Y., Kim, H.-J., Chung, S.-K., Dhong, H.-J., Kim, H.Y., Yim, Y.J., Kim, S.T., Jeon, P., Ko, Y.-H.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1042</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] Sinonasal Organized Hematoma: CT and MR Imaging Findings]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1208</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1204</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1209?rss=1">
<title><![CDATA[[HEAD & NECK] MR Imaging of Nonmalignant Polyps and Masses of the Nasopharynx and Sphenoid Sinus after Radiotherapy for Nasopharyngeal Carcinoma]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1209?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> The development of a new polyp or mass in the radiation field of a previously treated carcinoma is usually an ominous sign of a recurrent cancer, but rarely may it be caused instead by a nonmalignant process. The purpose of this study was to document the MR appearance of unusual nonmalignant polyps or masses (NMPMs) in the nasopharynx and sphenoid sinus arising after radiation treatment of nasopharyngeal carcinoma.</P>
<P><B>MATERIALS AND METHODS:</B> The MR imaging reports of patients undergoing imaging after radiation therapy for nasopharyngeal carcinoma were reviewed retrospectively to identify patients with unusual polyps and masses in the nasopharynx. The MR images of those patients with no evidence of malignancy on biopsy or follow-up were reviewed.</P>
<P><B>RESULTS:</B> The MR imaging reports of 1282 patients were reviewed, and 11 patients (1%) with NMPMs in the nasopharynx or sphenoid sinus were identified. Two patterns were identified: contrast enhancing nasopharyngeal polyps ranging in size from 1 to 5 cm (<I>n</I> = 5) and sphenoid sinus masses consisting of a nonenhancing mass filling a nonexpanded sinus (<I>n</I> = 4) and a heterogeneous enhancing mass expanding the sinus (<I>n</I> = 2). Osteoradionecrosis produced a large defect in the roof of the nasopharynx causing direct communication with the sphenoid sinus (<I>n</I> = 6). Histology revealed granulation tissue in all of the patients with variable amounts of fibrin and inflammatory cells. A direct infective etiology was not proved in any patient.</P>
<P><B>CONCLUSION:</B> NMPMs in the nasopharynx and sphenoid sinus are rare complications after radiation therapy to the skull base, but the radiologist needs to be aware of their appearance so that they can be considered in the differential diagnosis of suspected tumor recurrence.</P>
]]></description>
<dc:creator><![CDATA[King, A.D., Ahuja, A.T., Leung, S.-F., Abrigo, J., Wong, J.K.T., Poon, W.S., Woo, K.S., Chan, H.S., Tse, G.M.K.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1043</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] MR Imaging of Nonmalignant Polyps and Masses of the Nasopharynx and Sphenoid Sinus after Radiotherapy for Nasopharyngeal Carcinoma]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1214</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1209</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1215?rss=1">
<title><![CDATA[[HEAD & NECK] The Frontal Intersinus Septal Air Cell: A New Hypothesis of Its Origin]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1215?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Air cells are often seen within the frontal intersinus septum. These cells have traditionally been thought to arise from displaced ethmoid cells from the frontal recess. This study explores the possibility that such cells may actually be diverticula from the frontal sinuses themselves and not of a direct ethmoid origin.</P>
<P><B>MATERIALS AND METHODS:</B> A prospective study of 200 consecutive CT scans in the coronal and axial planes was performed on patients without a history of recent trauma. The images were interpreted independently by a radiologist and an otolaryngologist. The CT studies were evaluated for the presence of a central intersinus septal air cell. If such a cell was identified, it was further classified as either being completely isolated from both frontal sinuses by a bony rim or as a communicating diverticulum from one of the frontal sinuses. If a central cell was present, it was also assessed for how much of the height of the intersinus septum it involved (lower one-half or full height).</P>
<P><B>RESULTS:</B> There was a complete concordance of the results between the 2 observers. An intersinus septal air cell was seen in 61 (30.5%) of the 200 cases, and 85.3% of these cells were clearly seen to communicate anteromedially with either one of the frontal sinuses or both frontal sinuses (3 cases). In 9 (4.5%) of the 200 cases, the central cell had no demonstrable connection to either frontal sinus. Of the 61 cases with a central cell, 55 (90.16%) of the cells occupied the full height of the septum, and 6 (9.84%) only involved the lower half of the septum.</P>
<P><B>CONCLUSION:</B> Contrary to the present convention that frontal intersinus septal cells originate as displaced ethmoid cells from the frontal recess, we found that most such cells are actually diverticula from the frontal sinuses themselves.</P>
]]></description>
<dc:creator><![CDATA[Som, P.M., Lawson, W.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1057</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] The Frontal Intersinus Septal Air Cell: A New Hypothesis of Its Origin]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1217</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1215</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1218?rss=1">
<title><![CDATA[[HEAD & NECK] Paratracheal Air Cysts: A Common Finding on Routine CT Examinations of the Cervical Spine and Neck That May Mimic Pneumomediastinum in Patients With Traumatic Injuries]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1218?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Collections of extraluminal paratracheal gas may be present on CT images of the neck and cervical spine and the radiologist may question whether this is related to a pathologic process. This study is designed to demonstrate the appearance, clinical presentation, and prevalence of paratracheal air cysts, which, on CT examinations of the neck, can mimic abnormal extraluminal air.</P>
<P><B>MATERIALS AND METHODS:</B> From January 1, 2005, through May 22, 2005, a total of 702 CT examinations of the cervical spine or soft tissue of the neck were reviewed. All examinations were at 2- to 5-mm thickness. Sagittal and coronal reconstructions were available for review, if necessary. Paratracheal air cysts were evaluated for size; the presence of visible communication with the trachea; association with pneumothorax, pneumomediastinum, or subcutaneous emphysema; and association with findings of emphysematous changes in the lung apices. Patient demographics of age, sex, and whether the patient had sustained a traumatic injury were also collected.</P>
<P><B>RESULTS:</B> Of the 702 patients evaluated, 26 (3.7%) had paratracheal air cysts, all of which were found on the right, at the level of the thoracic inlet. Ages of the patients ranged from 15 to 74 years. In 9 (34.6%) of the patients, a direct communication with the trachea was seen. Sizes of the paratracheal air cysts ranged from 1 <FONT FACE="arial,helvetica">x</FONT> 2 mm to 10 <FONT FACE="arial,helvetica">x</FONT> 15 mm. No association was found with CT findings of emphysema in the lung apices, abnormal soft tissue air, or trauma.</P>
<P><B>CONCLUSION:</B> Right paratracheal air cysts are a common CT finding that occur in a predictable location. In the setting of trauma, these characteristic structures can mimic pneumomediastinum and are seen in approximately 3% to 4% of the US population. The cause is unclear but may be either congenital or an acquired phenomenon, given that they are often seen in both children and adults. We found no association with either trauma or the presence of emphysematous changes in the lung apices.</P>
]]></description>
<dc:creator><![CDATA[Buterbaugh, J.E., Erly, W.K.]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1058</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] Paratracheal Air Cysts: A Common Finding on Routine CT Examinations of the Cervical Spine and Neck That May Mimic Pneumomediastinum in Patients With Traumatic Injuries]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1221</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1218</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1222?rss=1">
<title><![CDATA[[ACR APPROPRIATENESS CRITERIA] Epilepsy]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1222?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Karis, J.P., for the Expert Panel on Neurologic Imaging]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/</dc:identifier>
<dc:title><![CDATA[[ACR APPROPRIATENESS CRITERIA] Epilepsy]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1224</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1222</prism:startingPage>
<prism:section>ACR APPROPRIATENESS CRITERIA</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/6/1225?rss=1">
<title><![CDATA[[SOCIETY PRESIDENT BIOGRAPHIES] SOCIETY PRESIDENT BIOGRAPHIES]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/6/1225?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-06-10</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1200</dc:identifier>
<dc:title><![CDATA[[SOCIETY PRESIDENT BIOGRAPHIES] SOCIETY PRESIDENT BIOGRAPHIES]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1226</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>1225</prism:startingPage>
<prism:section>SOCIETY PRESIDENT BIOGRAPHIES</prism:section>
</item>

</rdf:RDF>