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<meta name="DC.Title" content="Sturge-Weber syndrome: cranial MR imaging with Gd-DTPA." />
<meta name="DC.Date" content="1993-03-01" />
<meta name="DC.Publisher" content="American Journal of Neuroradiology" />
<meta name="DC.Rights" content="Copyright © American Society of Neuroradiology" />
<meta name="DC.AccessRights" content="restricted" />
<meta name="DC.Description" content="PURPOSE To study the role of Gd-DTPA in cranial MR of patients with Sturge-Weber syndrome.

METHODS AND MATERIALS Seven patients with Sturge-Weber syndrome, ages 3 months to 36 years, were evaluated with unenhanced and contrast-enhanced (Gd-DTPA) MR imaging. Correlation was made to cranial CT in five patients.

RESULTS MR findings included (in decreasing frequency): pial angiomatosis, cerebral atrophy, decrease in cortical veins, enlargement of deep veins, enlargement of choroid plexus, and parenchymal calcification. Contrast MR imaging was essential in diagnosis in four cases in which cranial CT, unenhanced MR, or angiography was normal or demonstrated nonspecific abnormalities. Pial angiomatosis with adjacent cerebral atrophy were the only consistent radiographic abnormalities.

CONCLUSION In all patients, contrast MR demonstrated the radiographic spectrum of central nervous system abnormalities in Sturge-Weber syndrome to a greater degree than unenhanced MR or CT and may represent the method of diagnosis in these patients. Demonstration of the pial angioma on contrast MR should be considered the most important criterion for the radiographic diagnosis of Sturge-Weber syndrome." />
<meta name="DC.Contributor" content="R A Benedikt" />
<meta name="DC.Contributor" content="D C Brown" />
<meta name="DC.Contributor" content="R Walker" />
<meta name="DC.Contributor" content="V N Ghaed" />
<meta name="DC.Contributor" content="M Mitchell" />
<meta name="DC.Contributor" content="C A Geyer" />
<meta name="article:published_time" content="1993-03-01" />
<meta name="citation_title" content="Sturge-Weber syndrome: cranial MR imaging with Gd-DTPA." />
<meta name="citation_abstract" lang="en" content="&lt;h3&gt;PURPOSE&lt;/h3&gt;
&lt;p&gt;To study the role of Gd-DTPA in cranial MR of patients with Sturge-Weber syndrome.&lt;/p&gt;&lt;h3&gt;METHODS AND MATERIALS&lt;/h3&gt;
&lt;p&gt;Seven patients with Sturge-Weber syndrome, ages 3 months to 36 years, were evaluated with unenhanced and contrast-enhanced (Gd-DTPA) MR imaging. Correlation was made to cranial CT in five patients.&lt;/p&gt;&lt;h3&gt;RESULTS&lt;/h3&gt;
&lt;p&gt;MR findings included (in decreasing frequency): pial angiomatosis, cerebral atrophy, decrease in cortical veins, enlargement of deep veins, enlargement of choroid plexus, and parenchymal calcification. Contrast MR imaging was essential in diagnosis in four cases in which cranial CT, unenhanced MR, or angiography was normal or demonstrated nonspecific abnormalities. Pial angiomatosis with adjacent cerebral atrophy were the only consistent radiographic abnormalities.&lt;/p&gt;&lt;h3&gt;CONCLUSION&lt;/h3&gt;
&lt;p&gt;In all patients, contrast MR demonstrated the radiographic spectrum of central nervous system abnormalities in Sturge-Weber syndrome to a greater degree than unenhanced MR or CT and may represent the method of diagnosis in these patients. Demonstration of the pial angioma on contrast MR should be considered the most important criterion for the radiographic diagnosis of Sturge-Weber syndrome.&lt;/p&gt;" />
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<meta name="citation_publication_date" content="1993/03/01" />
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<meta name="citation_author" content="R A Benedikt" />
<meta name="citation_author_institution" content="Department of Radiology, Walter Reed Army Medical Center, Washington, DC 20307-5001." />
<meta name="citation_author" content="D C Brown" />
<meta name="citation_author_institution" content="Department of Radiology, Walter Reed Army Medical Center, Washington, DC 20307-5001." />
<meta name="citation_author" content="R Walker" />
<meta name="citation_author_institution" content="Department of Radiology, Walter Reed Army Medical Center, Washington, DC 20307-5001." />
<meta name="citation_author" content="V N Ghaed" />
<meta name="citation_author_institution" content="Department of Radiology, Walter Reed Army Medical Center, Washington, DC 20307-5001." />
<meta name="citation_author" content="M Mitchell" />
<meta name="citation_author_institution" content="Department of Radiology, Walter Reed Army Medical Center, Washington, DC 20307-5001." />
<meta name="citation_author" content="C A Geyer" />
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<meta name="twitter:title" content="Sturge-Weber syndrome: cranial MR imaging with Gd-DTPA." />
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<meta name="twitter:description" content="PURPOSE To study the role of Gd-DTPA in cranial MR of patients with Sturge-Weber syndrome.

METHODS AND MATERIALS Seven patients with Sturge-Weber syndrome, ages 3 months to 36 years, were evaluated with unenhanced and contrast-enhanced (Gd-DTPA) MR imaging. Correlation was made to cranial CT in five patients.

RESULTS MR findings included (in decreasing frequency): pial angiomatosis, cerebral atrophy, decrease in cortical veins, enlargement of deep veins, enlargement of choroid plexus, and parenchymal calcification. Contrast MR imaging was essential in diagnosis in four cases in which cranial CT, unenhanced MR, or angiography was normal or demonstrated nonspecific abnormalities. Pial angiomatosis with adjacent cerebral atrophy were the only consistent radiographic abnormalities.

CONCLUSION In all patients, contrast MR demonstrated the radiographic spectrum of central nervous system abnormalities in Sturge-Weber syndrome to a greater degree than unenhanced MR or CT and may represent the method of diagnosis in these patients. Demonstration of the pial angioma on contrast MR should be considered the most important criterion for the radiographic diagnosis of Sturge-Weber syndrome." />
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<meta name="og-description" property="og:description" content="PURPOSE To study the role of Gd-DTPA in cranial MR of patients with Sturge-Weber syndrome.

METHODS AND MATERIALS Seven patients with Sturge-Weber syndrome, ages 3 months to 36 years, were evaluated with unenhanced and contrast-enhanced (Gd-DTPA) MR imaging. Correlation was made to cranial CT in five patients.

RESULTS MR findings included (in decreasing frequency): pial angiomatosis, cerebral atrophy, decrease in cortical veins, enlargement of deep veins, enlargement of choroid plexus, and parenchymal calcification. Contrast MR imaging was essential in diagnosis in four cases in which cranial CT, unenhanced MR, or angiography was normal or demonstrated nonspecific abnormalities. Pial angiomatosis with adjacent cerebral atrophy were the only consistent radiographic abnormalities.

CONCLUSION In all patients, contrast MR demonstrated the radiographic spectrum of central nervous system abnormalities in Sturge-Weber syndrome to a greater degree than unenhanced MR or CT and may represent the method of diagnosis in these patients. Demonstration of the pial angioma on contrast MR should be considered the most important criterion for the radiographic diagnosis of Sturge-Weber syndrome." />
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      <h1 class="highwire-cite-title" id="page-title">Sturge-Weber syndrome: cranial MR imaging with Gd-DTPA.</h1>  
    	<div class="highwire-cite-authors"><span  class="highwire-citation-authors"><span class="highwire-citation-author first" data-delta="0">R A Benedikt</span>, <span class="highwire-citation-author" data-delta="1">D C Brown</span>, <span class="highwire-citation-author" data-delta="2">R Walker</span>, <span class="highwire-citation-author" data-delta="3">V N Ghaed</span>, <span class="highwire-citation-author" data-delta="4">M Mitchell</span> and <span class="highwire-citation-author" data-delta="5">C A Geyer</span></span></div>
  
    	<div class="highwire-cite-metadata"><span  class="highwire-cite-metadata-journal highwire-cite-metadata">American Journal of Neuroradiology </span><span  class="highwire-cite-metadata-date highwire-cite-metadata">March 1993,  </span><span  class="highwire-cite-metadata-volume highwire-cite-metadata">14 </span><span  class="highwire-cite-metadata-issue highwire-cite-metadata">(2) </span><span  class="highwire-cite-metadata-pages highwire-cite-metadata">409-415; </span></div>
  
  
  
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<div id="hw-article-author-popups-top-node-5717--6436908805" style="display: none;"><div class="author-tooltip-0"><div class="author-tooltip-name">R A Benedikt </div><div class="author-tooltip-affiliation"><span class="author-tooltip-text"><div class='author-affiliation'>Department of Radiology, Walter Reed Army Medical Center, Washington, DC 20307-5001.</div></span></div><ul class="author-tooltip-find-more"><li class="author-tooltip-gs-link first"><a href="/lookup/google-scholar?link_type=googlescholar&amp;gs_type=author&amp;author%5B0%5D=R%2BA%2BBenedikt%2B" target="_blank" class="" data-icon-position="" data-hide-link-title="0">Find this author on Google Scholar</a></li><li class="author-tooltip-pubmed-link"><a href="/lookup/external-ref?access_num=Benedikt%20RA&amp;link_type=AUTHORSEARCH" target="_blank" class="" data-icon-position="" data-hide-link-title="0">Find this author on PubMed</a></li><li class="author-site-search-link last"><a href="/search/author1%3AR%2BA%2BBenedikt%2B" 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