Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome
Identifieur interne : 002742 ( Istex/Corpus ); précédent : 002741; suivant : 002743Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome
Auteurs : Sharon W. WeissSource :
- Human Pathology [ 0046-8177 ] ; 1988.
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Abstract
Two infants with Turner's syndrome and an unusual vascular tumor or malformation of the feet are described. In one child, the lesion developed in the dorsal metacarpal area, whereas in the other, the lesion was located in a bilaterally symmetrical distribution over the dorsum of the feet. Both lesions were characterized by a proliferation of tortuous, thick-walled veins with imperfectly formed muscular walls. Redundancy of the endothelial lining leading to intimal “webs” and intraluminal vascular channels was prominent. The similarity of these two lesions clinically and histologically suggests that they do not represent a fortuitous occurrence, but an additional manifestation of Turner's syndrome. Furthermore, their existence indicates that the vascular abnormality in Turner's syndrome may be more generalized than previously recognized and may include abnormalities of peripheral blood vessels in addition to those of the heart and aorta. Hum Pathol 9:1015–1018. This is a US government work. There are
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DOI: 10.1016/S0046-8177(88)80079-0
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In one child, the lesion developed in the dorsal metacarpal area, whereas in the other, the lesion was located in a bilaterally symmetrical distribution over the dorsum of the feet. Both lesions were characterized by a proliferation of tortuous, thick-walled veins with imperfectly formed muscular walls. Redundancy of the endothelial lining leading to intimal “webs” and intraluminal vascular channels was prominent. The similarity of these two lesions clinically and histologically suggests that they do not represent a fortuitous occurrence, but an additional manifestation of Turner's syndrome. Furthermore, their existence indicates that the vascular abnormality in Turner's syndrome may be more generalized than previously recognized and may include abnormalities of peripheral blood vessels in addition to those of the heart and aorta. Hum Pathol 9:1015–1018. This is a US government work. There are</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>hemangioma</json:string><json:string>syndrome</json:string><json:string>lesion</json:string><json:string>soft tissue</json:string><json:string>additional manifestation</json:string><json:string>soft tissue pathology</json:string><json:string>forces institute</json:string><json:string>approximate magnification</json:string><json:string>elastic stains</json:string><json:string>government work</json:string><json:string>muscle layers</json:string><json:string>human pathology volume</json:string><json:string>overlying skin</json:string><json:string>lymphatic system</json:string><json:string>cystic hygroma</json:string><json:string>elastic stain</json:string><json:string>cavernous sinus</json:string><json:string>intimal changes</json:string></teeft></keywords><author><json:item><name>Sharon W. Weiss MD</name></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Turner's syndrome</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>hemangioma</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>lymphangioma</value></json:item></subject><articleId><json:string>88800790</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Two infants with Turner's syndrome and an unusual vascular tumor or malformation of the feet are described. In one child, the lesion developed in the dorsal metacarpal area, whereas in the other, the lesion was located in a bilaterally symmetrical distribution over the dorsum of the feet. Both lesions were characterized by a proliferation of tortuous, thick-walled veins with imperfectly formed muscular walls. Redundancy of the endothelial lining leading to intimal “webs” and intraluminal vascular channels was prominent. The similarity of these two lesions clinically and histologically suggests that they do not represent a fortuitous occurrence, but an additional manifestation of Turner's syndrome. Furthermore, their existence indicates that the vascular abnormality in Turner's syndrome may be more generalized than previously recognized and may include abnormalities of peripheral blood vessels in addition to those of the heart and aorta. Hum Pathol 9:1015–1018. This is a US government work. There are</abstract><qualityIndicators><score>4.415</score><pdfVersion>1.3</pdfVersion><pdfPageSize>590.28 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><keywordCount>3</keywordCount><abstractCharCount>1014</abstractCharCount><pdfWordCount>2627</pdfWordCount><pdfCharCount>10275</pdfCharCount><pdfPageCount>4</pdfPageCount><abstractWordCount>149</abstractWordCount></qualityIndicators><title>Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome</title><pii><json:string>S0046-8177(88)80079-0</json:string></pii><genre><json:string>research-article</json:string></genre><host><title>Human Pathology</title><language><json:string>unknown</json:string></language><publicationDate>1988</publicationDate><issn><json:string>0046-8177</json:string></issn><pii><json:string>S0046-8177(88)X8076-X</json:string></pii><volume>19</volume><issue>9</issue><pages><first>1015</first><last>1018</last></pages><genre><json:string>journal</json:string></genre></host><categories><wos><json:string>science</json:string><json:string>pathology</json:string></wos><scienceMetrix><json:string>health sciences</json:string><json:string>clinical medicine</json:string><json:string>pathology</json:string></scienceMetrix><inist><json:string>sciences appliquees, technologies et medecines</json:string><json:string>sciences biologiques et medicales</json:string><json:string>sciences medicales</json:string><json:string>gynecologie. andrologie. obstetrique</json:string></inist></categories><publicationDate>1988</publicationDate><copyrightDate>1988</copyrightDate><doi><json:string>10.1016/S0046-8177(88)80079-0</json:string></doi><id>5571393DC95C459826954F3F3732F4105F8DC8CB</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/5571393DC95C459826954F3F3732F4105F8DC8CB/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/5571393DC95C459826954F3F3732F4105F8DC8CB/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/5571393DC95C459826954F3F3732F4105F8DC8CB/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>ELSEVIER</publisher><availability><p>©1988 the W.B. Saunders Company. All rights reserved</p></availability><date>1988</date></publicationStmt><notesStmt><note>The opinions and assertions contained herein are the private views of the author and are not to be construed as official or as representing the view of the Department of the Army or the Department of Defense.</note><note>This is a US government work. There are no restrictions on its use.</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome</title><author xml:id="author-0000"><persName><forename type="first">Sharon W.</forename><surname>Weiss</surname></persName><roleName type="degree">MD</roleName><note type="biography">From the Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC.</note><affiliation>From the Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC.</affiliation></author><idno type="istex">5571393DC95C459826954F3F3732F4105F8DC8CB</idno><idno type="DOI">10.1016/S0046-8177(88)80079-0</idno><idno type="PII">S0046-8177(88)80079-0</idno><idno type="ArticleID">88800790</idno></analytic><monogr><title level="j">Human Pathology</title><title level="j" type="abbrev">YHUPA</title><idno type="pISSN">0046-8177</idno><idno type="PII">S0046-8177(88)X8076-X</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1988"></date><biblScope unit="volume">19</biblScope><biblScope unit="issue">9</biblScope><biblScope unit="page" from="1015">1015</biblScope><biblScope unit="page" to="1018">1018</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1988</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Two infants with Turner's syndrome and an unusual vascular tumor or malformation of the feet are described. In one child, the lesion developed in the dorsal metacarpal area, whereas in the other, the lesion was located in a bilaterally symmetrical distribution over the dorsum of the feet. Both lesions were characterized by a proliferation of tortuous, thick-walled veins with imperfectly formed muscular walls. Redundancy of the endothelial lining leading to intimal “webs” and intraluminal vascular channels was prominent. The similarity of these two lesions clinically and histologically suggests that they do not represent a fortuitous occurrence, but an additional manifestation of Turner's syndrome. Furthermore, their existence indicates that the vascular abnormality in Turner's syndrome may be more generalized than previously recognized and may include abnormalities of peripheral blood vessels in addition to those of the heart and aorta. Hum Pathol 9:1015–1018. This is a US government work. There are</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><item><term>Turner's syndrome</term></item><item><term>hemangioma</term></item><item><term>lymphangioma</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1988">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/5571393DC95C459826954F3F3732F4105F8DC8CB/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier doc found" wicri:toSee="Elsevier, no converted or simple article"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 5.0.1//EN//XML" URI="art501.dtd" name="istex:docType"></istex:docType><istex:document><article version="5.0" xml:lang="en" docsubtype="fla"><item-info><jid>YHUPA</jid><aid>88800790</aid><ce:pii>S0046-8177(88)80079-0</ce:pii><ce:doi>10.1016/S0046-8177(88)80079-0</ce:doi><ce:copyright type="unknown" year="1988">the W.B. Saunders Company. All rights reserved</ce:copyright></item-info><head><ce:article-footnote><ce:label>*</ce:label><ce:note-para>The opinions and assertions contained herein are the private views of the author and are not to be construed as official or as representing the view of the Department of the Army or the Department of Defense.</ce:note-para></ce:article-footnote><ce:article-footnote><ce:label>**</ce:label><ce:note-para>This is a US government work. There are no restrictions on its use.</ce:note-para></ce:article-footnote><ce:title>Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome</ce:title><ce:author-group><ce:author><ce:degrees>MD</ce:degrees><ce:given-name>Sharon W.</ce:given-name><ce:surname>Weiss</ce:surname><ce:cross-ref refid="fn1"><ce:sup>1</ce:sup></ce:cross-ref><ce:cross-ref refid="cor1"><ce:sup>*</ce:sup></ce:cross-ref></ce:author><ce:correspondence id="cor1"><ce:label>*</ce:label><ce:text>Address correspondence and reprint requests to Sharon W. Weiss, MD, Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000.</ce:text></ce:correspondence><ce:footnote id="fn1"><ce:label>1</ce:label><ce:note-para>From the Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC.</ce:note-para></ce:footnote></ce:author-group><ce:date-accepted day="8" month="12" year="1987"></ce:date-accepted><ce:abstract id="ab1" class="author" xml:lang="en"><ce:abstract-sec><ce:simple-para>Two infants with Turner's syndrome and an unusual vascular tumor or malformation of the feet are described. In one child, the lesion developed in the dorsal metacarpal area, whereas in the other, the lesion was located in a bilaterally symmetrical distribution over the dorsum of the feet. Both lesions were characterized by a proliferation of tortuous, thick-walled veins with imperfectly formed muscular walls. Redundancy of the endothelial lining leading to intimal “webs” and intraluminal vascular channels was prominent. The similarity of these two lesions clinically and histologically suggests that they do not represent a fortuitous occurrence, but an additional manifestation of Turner's syndrome. Furthermore, their existence indicates that the vascular abnormality in Turner's syndrome may be more generalized than previously recognized and may include abnormalities of peripheral blood vessels in addition to those of the heart and aorta. <ce:small-caps>Hum Pathol</ce:small-caps> 9:1015–1018. This is a US government work. 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Tumors</sb:maintitle></sb:title></sb:contribution><sb:host><sb:edited-book><sb:date>1983</sb:date><sb:publisher><sb:name>Mosby</sb:name><sb:location>St Louis</sb:location></sb:publisher></sb:edited-book><sb:pages><sb:first-page>379</sb:first-page><sb:last-page>421</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference></ce:bibliography-sec></ce:bibliography></tail></article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Pedal hemangioma (venous malformation) occurring in Turner's syndrome: An additional manifestation of the syndrome</title></titleInfo><name type="personal"><namePart type="given">Sharon W.</namePart><namePart type="family">Weiss</namePart><namePart type="termsOfAddress">MD</namePart><description>From the Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC.</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1988</dateIssued><copyrightDate encoding="w3cdtf">1988</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Two infants with Turner's syndrome and an unusual vascular tumor or malformation of the feet are described. In one child, the lesion developed in the dorsal metacarpal area, whereas in the other, the lesion was located in a bilaterally symmetrical distribution over the dorsum of the feet. Both lesions were characterized by a proliferation of tortuous, thick-walled veins with imperfectly formed muscular walls. Redundancy of the endothelial lining leading to intimal “webs” and intraluminal vascular channels was prominent. The similarity of these two lesions clinically and histologically suggests that they do not represent a fortuitous occurrence, but an additional manifestation of Turner's syndrome. Furthermore, their existence indicates that the vascular abnormality in Turner's syndrome may be more generalized than previously recognized and may include abnormalities of peripheral blood vessels in addition to those of the heart and aorta. Hum Pathol 9:1015–1018. This is a US government work. There are</abstract><note>The opinions and assertions contained herein are the private views of the author and are not to be construed as official or as representing the view of the Department of the Army or the Department of Defense.</note><note>This is a US government work. There are no restrictions on its use.</note><subject lang="en"><topic>Turner's syndrome</topic><topic>hemangioma</topic><topic>lymphangioma</topic></subject><relatedItem type="host"><titleInfo><title>Human Pathology</title></titleInfo><titleInfo type="abbreviated"><title>YHUPA</title></titleInfo><genre type="journal">journal</genre><originInfo><dateIssued encoding="w3cdtf">198809</dateIssued></originInfo><identifier type="ISSN">0046-8177</identifier><identifier type="PII">S0046-8177(88)X8076-X</identifier><part><date>198809</date><detail type="volume"><number>19</number><caption>vol.</caption></detail><detail type="issue"><number>9</number><caption>no.</caption></detail><extent unit="issue pages"><start>999</start><end>1124</end></extent><extent unit="pages"><start>1015</start><end>1018</end></extent></part></relatedItem><identifier type="istex">5571393DC95C459826954F3F3732F4105F8DC8CB</identifier><identifier type="DOI">10.1016/S0046-8177(88)80079-0</identifier><identifier type="PII">S0046-8177(88)80079-0</identifier><identifier type="ArticleID">88800790</identifier><accessCondition type="use and reproduction" contentType="copyright">©1988 the W.B. Saunders Company. All rights reserved</accessCondition><recordInfo><recordContentSource>ELSEVIER</recordContentSource><recordOrigin>the W.B. Saunders Company. All rights reserved, ©1988</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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