Massive localised lymphoedema: a rare vascular malformation
Identifieur interne : 003D11 ( Istex/Corpus ); précédent : 003D10; suivant : 003D12Massive localised lymphoedema: a rare vascular malformation
Auteurs : K J Williams ; M N Al-Sakkal ; A. Alsafi ; A H DaviesSource :
- BMJ Case Reports [ 1757-790X ] ; 2013-06-12.
Abstract
Lymphatic malformations are a subset of congenital vascular malformations, and are caused by a defect in lymphatic development during embryogenesis. When lymphatic mesoderm development is prematurely arrested, it retains it proliferative potential. Stimulus in the future can cause the lesion to proliferate locally without coordination or regulation, resulting in the rare condition known as massive localised lymphoedema (MLL). We present a case report of MLL, a rare and ill-defined soft tissue mass reported in the morbidly obese, with reference to the existing literature.
Url:
DOI: 10.1136/bcr-2013-010060
Links to Exploration step
ISTEX:81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title>Massive localised lymphoedema: a rare vascular malformation</title><author><name sortKey="Williams, K J" sort="Williams, K J" uniqKey="Williams K" first="K J" last="Williams">K J Williams</name><affiliation><mods:affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</mods:affiliation></affiliation></author><author><name sortKey="Al Sakkal, M N" sort="Al Sakkal, M N" uniqKey="Al Sakkal M" first="M N" last="Al-Sakkal">M N Al-Sakkal</name><affiliation><mods:affiliation>Department of Pathology, Imperial College London, London, UK</mods:affiliation></affiliation></author><author><name sortKey="Alsafi, A" sort="Alsafi, A" uniqKey="Alsafi A" first="A" last="Alsafi">A. Alsafi</name><affiliation><mods:affiliation>Department of Radiology, Imperial College London, London, UK</mods:affiliation></affiliation></author><author><name sortKey="Davies, A H" sort="Davies, A H" uniqKey="Davies A" first="A H" last="Davies">A H Davies</name><affiliation><mods:affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58</idno><date when="2013" year="2013">2013</date><idno type="doi">10.1136/bcr-2013-010060</idno><idno type="url">https://api.istex.fr/document/81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003D11</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">003D11</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a">Massive localised lymphoedema: a rare vascular malformation</title><author><name sortKey="Williams, K J" sort="Williams, K J" uniqKey="Williams K" first="K J" last="Williams">K J Williams</name><affiliation><mods:affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</mods:affiliation></affiliation></author><author><name sortKey="Al Sakkal, M N" sort="Al Sakkal, M N" uniqKey="Al Sakkal M" first="M N" last="Al-Sakkal">M N Al-Sakkal</name><affiliation><mods:affiliation>Department of Pathology, Imperial College London, London, UK</mods:affiliation></affiliation></author><author><name sortKey="Alsafi, A" sort="Alsafi, A" uniqKey="Alsafi A" first="A" last="Alsafi">A. Alsafi</name><affiliation><mods:affiliation>Department of Radiology, Imperial College London, London, UK</mods:affiliation></affiliation></author><author><name sortKey="Davies, A H" sort="Davies, A H" uniqKey="Davies A" first="A H" last="Davies">A H Davies</name><affiliation><mods:affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">BMJ Case Reports</title><title level="j" type="abbrev">BMJ Case Reports</title><idno type="eISSN">1757-790X</idno><imprint><publisher>BMJ Publishing Group Ltd</publisher><date type="published" when="2013-06-12">2013-06-12</date><biblScope unit="volume">2013</biblScope></imprint></series><idno type="istex">81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58</idno><idno type="DOI">10.1136/bcr-2013-010060</idno><idno type="href">casereports-2013-bcr-2013-010060.pdf</idno><idno type="ArticleID">bcr-2013-010060</idno><idno type="local">casereports;2013/jun12_1/bcr2013010060</idno></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract">Lymphatic malformations are a subset of congenital vascular malformations, and are caused by a defect in lymphatic development during embryogenesis. When lymphatic mesoderm development is prematurely arrested, it retains it proliferative potential. Stimulus in the future can cause the lesion to proliferate locally without coordination or regulation, resulting in the rare condition known as massive localised lymphoedema (MLL). We present a case report of MLL, a rare and ill-defined soft tissue mass reported in the morbidly obese, with reference to the existing literature.</div></front></TEI><istex><corpusName>bmj</corpusName><keywords><teeft><json:string>malformation</json:string><json:string>lymphatic</json:string><json:string>lymphoedema</json:string><json:string>localised</json:string><json:string>morbidly</json:string><json:string>brous</json:string><json:string>clinician</json:string><json:string>gure</json:string><json:string>imperial college london</json:string><json:string>surg</json:string><json:string>lymphedema</json:string><json:string>septae</json:string><json:string>brous septae</json:string><json:string>pathol</json:string><json:string>massive localised lymphoedema</json:string><json:string>congenital</json:string><json:string>soft tissue mass</json:string><json:string>localised lymphoedema</json:string><json:string>clinical entity characterised</json:string><json:string>deranged lymphatic drainage</json:string><json:string>fatty lobules</json:string><json:string>pseudocyst formation</json:string><json:string>soft tissue tumors</json:string><json:string>malignant transformation</json:string><json:string>surgical excision</json:string><json:string>obesity epidemic</json:string><json:string>further permission</json:string><json:string>correct approach</json:string><json:string>lesion</json:string><json:string>recurrence</json:string></teeft></keywords><author><json:item><name>K J Williams</name><affiliations><json:string>Academic Section of Vascular Surgery, Imperial College London, London, UK</json:string></affiliations></json:item><json:item><name>M N Al-Sakkal</name><affiliations><json:string>Department of Pathology, Imperial College London, London, UK</json:string></affiliations></json:item><json:item><name>A Alsafi</name><affiliations><json:string>Department of Radiology, Imperial College London, London, UK</json:string></affiliations></json:item><json:item><name>A H Davies</name><affiliations><json:string>Academic Section of Vascular Surgery, Imperial College London, London, UK</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Rare disease</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Female</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>51-70 years</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Middle-East</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Surgery</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Rare disease</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>General surgery</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Vascular surgery</value></json:item></subject><articleId><json:string>bcr-2013-010060</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>case-report</json:string></originalGenre><abstract>Lymphatic malformations are a subset of congenital vascular malformations, and are caused by a defect in lymphatic development during embryogenesis. When lymphatic mesoderm development is prematurely arrested, it retains it proliferative potential. Stimulus in the future can cause the lesion to proliferate locally without coordination or regulation, resulting in the rare condition known as massive localised lymphoedema (MLL). We present a case report of MLL, a rare and ill-defined soft tissue mass reported in the morbidly obese, with reference to the existing literature.</abstract><qualityIndicators><score>2.62</score><pdfVersion>1.3</pdfVersion><pdfPageSize>595.276 x 793.701 pts</pdfPageSize><refBibsNative>true</refBibsNative><keywordCount>8</keywordCount><abstractCharCount>577</abstractCharCount><pdfWordCount>1624</pdfWordCount><pdfCharCount>10767</pdfCharCount><pdfPageCount>3</pdfPageCount><abstractWordCount>83</abstractWordCount></qualityIndicators><title>Massive localised lymphoedema: a rare vascular malformation</title><genre><json:string>case-report</json:string></genre><host><title>BMJ Case Reports</title><language><json:string>unknown</json:string></language><eissn><json:string>1757-790X</json:string></eissn><publisherId><json:string>bmjcasereports</json:string></publisherId><volume>2013</volume><genre><json:string>journal</json:string></genre></host><categories><inist><json:string>sciences appliquees, technologies et medecines</json:string><json:string>sciences biologiques et medicales</json:string><json:string>sciences medicales</json:string></inist></categories><publicationDate>2013</publicationDate><copyrightDate>2013</copyrightDate><doi><json:string>10.1136/bcr-2013-010060</json:string></doi><id>81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a">Massive localised lymphoedema: a rare vascular malformation</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>BMJ Publishing Group Ltd</publisher><availability><p>2013 BMJ Publishing Group Ltd</p></availability><date>2013</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a">Massive localised lymphoedema: a rare vascular malformation</title><author xml:id="author-1"><persName><forename type="first">K J</forename><surname>Williams</surname></persName><affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</affiliation></author><author xml:id="author-2"><persName><forename type="first">M N</forename><surname>Al-Sakkal</surname></persName><affiliation>Department of Pathology, Imperial College London, London, UK</affiliation></author><author xml:id="author-3"><persName><forename type="first">A</forename><surname>Alsafi</surname></persName><affiliation>Department of Radiology, Imperial College London, London, UK</affiliation></author><author xml:id="author-4"><persName><forename type="first">A H</forename><surname>Davies</surname></persName><affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</affiliation></author></analytic><monogr><title level="j">BMJ Case Reports</title><title level="j" type="abbrev">BMJ Case Reports</title><idno type="eISSN">1757-790X</idno><imprint><publisher>BMJ Publishing Group Ltd</publisher><date type="published" when="2013-06-12"></date><biblScope unit="volume">2013</biblScope></imprint></monogr><idno type="istex">81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58</idno><idno type="DOI">10.1136/bcr-2013-010060</idno><idno type="href">casereports-2013-bcr-2013-010060.pdf</idno><idno type="ArticleID">bcr-2013-010060</idno><idno type="local">casereports;2013/jun12_1/bcr2013010060</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2013</date></creation><langUsage><language ident="en">en</language></langUsage><abstract><p>Lymphatic malformations are a subset of congenital vascular malformations, and are caused by a defect in lymphatic development during embryogenesis. When lymphatic mesoderm development is prematurely arrested, it retains it proliferative potential. Stimulus in the future can cause the lesion to proliferate locally without coordination or regulation, resulting in the rare condition known as massive localised lymphoedema (MLL). We present a case report of MLL, a rare and ill-defined soft tissue mass reported in the morbidly obese, with reference to the existing literature.</p></abstract><textClass><keywords scheme="keyword"><list><head>case-report-type</head><item><term>Rare disease</term></item></list></keywords></textClass><textClass><keywords scheme="keyword"><list><head>search-fields</head><item><term>Europe (West)</term></item><item><term>Female</term></item><item><term>51-70 years</term></item><item><term>Middle-East</term></item></list></keywords></textClass><textClass><keywords scheme="keyword"><list><head>hwp-journal-coll</head><item><term>Surgery</term></item></list></keywords></textClass><textClass><keywords scheme="keyword"><list><head>hwp-journal-coll</head><item><term>Rare disease</term></item></list></keywords></textClass><textClass><keywords scheme="keyword"><list><head>hwp-journal-coll</head><item><term>General surgery</term></item></list></keywords></textClass><textClass><keywords scheme="keyword"><list><head>hwp-journal-coll</head><item><term>Vascular surgery</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2013-06-12">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="corpus bmj" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="no"</istex:xmlDeclaration><istex:docType PUBLIC="-//NLM//DTD Journal Archiving and Interchange DTD v2.3 20070202//EN" URI="archivearticle.dtd" name="istex:docType"></istex:docType><istex:document><article article-type="case-report"><front><journal-meta><journal-id journal-id-type="hwp">casereports</journal-id><journal-id journal-id-type="publisher-id">bmjcasereports</journal-id><journal-title>BMJ Case Reports</journal-title><abbrev-journal-title abbrev-type="publisher">BMJ Case Reports</abbrev-journal-title><issn pub-type="epub">1757-790X</issn><publisher><publisher-name>BMJ Publishing Group Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">bcr-2013-010060</article-id><article-id pub-id-type="doi">10.1136/bcr-2013-010060</article-id><article-id pub-id-type="other">casereports;2013/jun12_1/bcr2013010060</article-id><article-id pub-id-type="other">casereports;bcr-2013-010060</article-id><article-id pub-id-type="other">jun12_1</article-id><article-id pub-id-type="other">bcr-2013-010060</article-id><article-id pub-id-type="other">bcr-2013-010060</article-id><article-categories><subj-group subj-group-type="case-report-type"><subject>Rare disease</subject></subj-group><subj-group subj-group-type="search-fields"><subject content-type="sex">Female</subject><subject content-type="age">51-70 years</subject><subject content-type="ethnicity">Middle-East</subject><subject content-type="region">Europe (West)</subject></subj-group><subj-group subj-group-type="hwp-journal-coll"><subject>Surgery</subject></subj-group><subj-group subj-group-type="hwp-journal-coll"><subject>Rare disease</subject></subj-group><subj-group subj-group-type="hwp-journal-coll"><subject>General surgery</subject></subj-group><subj-group subj-group-type="hwp-journal-coll"><subject>Vascular surgery</subject></subj-group><series-title>CASE REPORT</series-title></article-categories><title-group><article-title>Massive localised lymphoedema: a rare vascular malformation</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Williams</surname><given-names>K J</given-names></name><xref ref-type="aff" rid="af1">1</xref></contrib><contrib contrib-type="author"><name><surname>Al-Sakkal</surname><given-names>M N</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Alsafi</surname><given-names>A</given-names></name><xref ref-type="aff" rid="af3">3</xref></contrib><contrib contrib-type="author"><name><surname>Davies</surname><given-names>A H</given-names></name><xref ref-type="aff" rid="af1">1</xref></contrib></contrib-group><aff id="af1"><label>1</label><addr-line>Academic Section of Vascular Surgery</addr-line>, <institution>Imperial College London</institution>, <addr-line>London</addr-line>, <country>UK</country></aff><aff id="af2"><label>2</label><addr-line>Department of Pathology</addr-line>, <institution>Imperial College London</institution>, <addr-line>London</addr-line>, <country>UK</country></aff><aff id="af3"><label>3</label><addr-line>Department of Radiology</addr-line>, <institution>Imperial College London</institution>, <addr-line>London</addr-line>, <country>UK</country></aff><author-notes><corresp><label>Corresponding to</label> KJ Williams, <email>k.williams@imperial.ac.uk</email></corresp></author-notes><pub-date pub-type="collection"><year>2013</year></pub-date><pub-date pub-type="epub-original"><day>12</day><month>6</month><year>2013</year></pub-date><volume>2013</volume><volume-id pub-id-type="other">2013</volume-id><volume-id pub-id-type="other">2013</volume-id><elocation-id>bcr2013010060</elocation-id><permissions><copyright-statement>2013 BMJ Publishing Group Ltd</copyright-statement><copyright-year>2013</copyright-year></permissions><self-uri content-type="pdf" xlink:role="full-text" xlink:href="casereports-2013-bcr-2013-010060.pdf"></self-uri><abstract><p>Lymphatic malformations are a subset of congenital vascular malformations, and are caused by a defect in lymphatic development during embryogenesis. When lymphatic mesoderm development is prematurely arrested, it retains it proliferative potential. Stimulus in the future can cause the lesion to proliferate locally without coordination or regulation, resulting in the rare condition known as massive localised lymphoedema (MLL). We present a case report of MLL, a rare and ill-defined soft tissue mass reported in the morbidly obese, with reference to the existing literature.</p></abstract></article-meta></front></article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Massive localised lymphoedema: a rare vascular malformation</title><partName>CASE REPORT</partName></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Massive localised lymphoedema: a rare vascular malformation</title><partName>CASE REPORT</partName></titleInfo><name type="personal"><namePart type="given">K J</namePart><namePart type="family">Williams</namePart><affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M N</namePart><namePart type="family">Al-Sakkal</namePart><affiliation>Department of Pathology, Imperial College London, London, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A</namePart><namePart type="family">Alsafi</namePart><affiliation>Department of Radiology, Imperial College London, London, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A H</namePart><namePart type="family">Davies</namePart><affiliation>Academic Section of Vascular Surgery, Imperial College London, London, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="case-report" displayLabel="case-report"></genre><subject><genre>case-report-type</genre><topic>Rare disease</topic></subject><subject><genre>search-fields</genre><topic>Female</topic><topic>51-70 years</topic><topic>Middle-East</topic><geographic>Europe (West)</geographic></subject><subject><genre>hwp-journal-coll</genre><topic>Surgery</topic></subject><subject><genre>hwp-journal-coll</genre><topic>Rare disease</topic></subject><subject><genre>hwp-journal-coll</genre><topic>General surgery</topic></subject><subject><genre>hwp-journal-coll</genre><topic>Vascular surgery</topic></subject><originInfo><publisher>BMJ Publishing Group Ltd</publisher><dateIssued encoding="w3cdtf">2013-06-12</dateIssued><copyrightDate encoding="w3cdtf">2013</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>Lymphatic malformations are a subset of congenital vascular malformations, and are caused by a defect in lymphatic development during embryogenesis. When lymphatic mesoderm development is prematurely arrested, it retains it proliferative potential. Stimulus in the future can cause the lesion to proliferate locally without coordination or regulation, resulting in the rare condition known as massive localised lymphoedema (MLL). We present a case report of MLL, a rare and ill-defined soft tissue mass reported in the morbidly obese, with reference to the existing literature.</abstract><relatedItem type="host"><titleInfo><title>BMJ Case Reports</title></titleInfo><titleInfo type="abbreviated"><title>BMJ Case Reports</title></titleInfo><genre type="journal">journal</genre><identifier type="eISSN">1757-790X</identifier><identifier type="PublisherID">bmjcasereports</identifier><identifier type="PublisherID-hwp">casereports</identifier><part><date>2013</date><detail type="volume"><caption>vol.</caption><number>2013</number></detail></part></relatedItem><identifier type="istex">81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58</identifier><identifier type="DOI">10.1136/bcr-2013-010060</identifier><identifier type="href">casereports-2013-bcr-2013-010060.pdf</identifier><identifier type="ArticleID">bcr-2013-010060</identifier><identifier type="local">casereports;2013/jun12_1/bcr2013010060</identifier><accessCondition type="use and reproduction" contentType="copyright">2013 BMJ Publishing Group Ltd</accessCondition><recordInfo><recordContentSource>BMJ</recordContentSource></recordInfo></mods></metadata><annexes><json:item><extension>jpeg</extension><original>true</original><mimetype>image/jpeg</mimetype><uri>https://api.istex.fr/document/81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58/annexes/jpeg</uri></json:item></annexes><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003D11 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 003D11 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:81A221CD94A5CFA35B3CF8A0922D7AAA0A065E58
|texte= Massive localised lymphoedema: a rare vascular malformation
}}
| This area was generated with Dilib version V0.6.31. |  |