Lymphedema-induced lymphangiosarcoma
Identifieur interne : 001F69 ( Istex/Corpus ); précédent : 001F68; suivant : 001F70Lymphedema-induced lymphangiosarcoma
Auteurs : Arieke J. Janse ; Frits Van Coevorden ; Hans Peterse ; Ronald B. Keus ; Johannes A. Van DongenSource :
- European Journal of Surgical Oncology [ 0748-7983 ] ; 1995.
English descriptors
Abstract
A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.
Url:
DOI: 10.1016/S0748-7983(95)90270-8
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ISTEX:4502C1F68AAC9866DC15F684D509EDBAA88ECF0FLe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Lymphedema-induced lymphangiosarcoma</title><author><name sortKey="Janse, Arieke J" sort="Janse, Arieke J" uniqKey="Janse A" first="Arieke J." last="Janse">Arieke J. Janse</name><affiliation><mods:affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Coevorden, Frits Van" sort="Coevorden, Frits Van" uniqKey="Coevorden F" first="Frits Van" last="Coevorden">Frits Van Coevorden</name><affiliation><mods:affiliation>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.</mods:affiliation></affiliation></author><author><name sortKey="Peterse, Hans" sort="Peterse, Hans" uniqKey="Peterse H" first="Hans" last="Peterse">Hans Peterse</name><affiliation><mods:affiliation>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Keus, Ronald B" sort="Keus, Ronald B" uniqKey="Keus R" first="Ronald B." last="Keus">Ronald B. Keus</name><affiliation><mods:affiliation>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Dongen, Johannes A Van" sort="Dongen, Johannes A Van" uniqKey="Dongen J" first="Johannes A. Van" last="Dongen">Johannes A. Van Dongen</name><affiliation><mods:affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:4502C1F68AAC9866DC15F684D509EDBAA88ECF0F</idno><date when="1995" year="1995">1995</date><idno type="doi">10.1016/S0748-7983(95)90270-8</idno><idno type="url">https://api.istex.fr/document/4502C1F68AAC9866DC15F684D509EDBAA88ECF0F/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">001F69</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001F69</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Lymphedema-induced lymphangiosarcoma</title><author><name sortKey="Janse, Arieke J" sort="Janse, Arieke J" uniqKey="Janse A" first="Arieke J." last="Janse">Arieke J. Janse</name><affiliation><mods:affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Coevorden, Frits Van" sort="Coevorden, Frits Van" uniqKey="Coevorden F" first="Frits Van" last="Coevorden">Frits Van Coevorden</name><affiliation><mods:affiliation>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.</mods:affiliation></affiliation></author><author><name sortKey="Peterse, Hans" sort="Peterse, Hans" uniqKey="Peterse H" first="Hans" last="Peterse">Hans Peterse</name><affiliation><mods:affiliation>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Keus, Ronald B" sort="Keus, Ronald B" uniqKey="Keus R" first="Ronald B." last="Keus">Ronald B. Keus</name><affiliation><mods:affiliation>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Dongen, Johannes A Van" sort="Dongen, Johannes A Van" uniqKey="Dongen J" first="Johannes A. Van" last="Dongen">Johannes A. Van Dongen</name><affiliation><mods:affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">European Journal of Surgical Oncology</title><title level="j" type="abbrev">YEJSO</title><idno type="ISSN">0748-7983</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1995">1995</date><biblScope unit="volume">21</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="155">155</biblScope><biblScope unit="page" to="158">158</biblScope></imprint><idno type="ISSN">0748-7983</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0748-7983</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Stewart-Treves syndrome</term><term>angiosarcoma</term><term>breast carcinoma</term><term>lymphangiosarcoma</term><term>lymphedema</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>lymphangiosarcoma</json:string><json:string>lymphedema</json:string><json:string>radiotherapy</json:string><json:string>mastectomy</json:string><json:string>postmastectomy</json:string><json:string>chest wall</json:string><json:string>axillary</json:string><json:string>axilla</json:string><json:string>chemotherapy</json:string><json:string>abnormality</json:string><json:string>lymphedematous</json:string><json:string>postmastectomy lymphangiosarcoma</json:string><json:string>parasternal</json:string><json:string>breast cancer mast</json:string><json:string>breast cancer</json:string><json:string>sarcoma</json:string><json:string>chronic lymphedema</json:string><json:string>postmastectomy lymphedema</json:string><json:string>angiosarcoma</json:string><json:string>lesion</json:string><json:string>congenital lymphedema</json:string><json:string>forequarter amputation</json:string><json:string>parasternal area</json:string><json:string>median survival</json:string><json:string>netherlands cancer institute</json:string><json:string>primary site</json:string><json:string>edematous extremity</json:string><json:string>upper extremity</json:string><json:string>clinical course</json:string><json:string>slow locoregional progression</json:string><json:string>surgical exploration</json:string><json:string>range years</json:string><json:string>fatal outcome</json:string><json:string>therapeutic options</json:string><json:string>malignant melanoma</json:string><json:string>pathological examination</json:string><json:string>netherlands cancer</json:string><json:string>temporary improvement</json:string><json:string>unusual localization</json:string><json:string>skin abnormalities</json:string><json:string>extensive spread</json:string><json:string>nach brustkrebsoperation</json:string><json:string>syndrome</json:string><json:string>congenital</json:string></teeft></keywords><author><json:item><name>Arieke J. Janse</name><affiliations><json:string>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</json:string></affiliations></json:item><json:item><name>Frits van Coevorden</name><affiliations><json:string>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.</json:string></affiliations></json:item><json:item><name>Hans Peterse</name><affiliations><json:string>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</json:string></affiliations></json:item><json:item><name>Ronald B. Keus</name><affiliations><json:string>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</json:string></affiliations></json:item><json:item><name>Johannes A. van Dongen</name><affiliations><json:string>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>lymphangiosarcoma</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>angiosarcoma</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Stewart-Treves syndrome</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>breast carcinoma</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>lymphedema</value></json:item></subject><articleId><json:string>95902708</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.</abstract><qualityIndicators><score>3.352</score><pdfVersion>1.3</pdfVersion><pdfPageSize>612 x 828 pts</pdfPageSize><refBibsNative>true</refBibsNative><keywordCount>5</keywordCount><abstractCharCount>671</abstractCharCount><pdfWordCount>2236</pdfWordCount><pdfCharCount>14709</pdfCharCount><pdfPageCount>4</pdfPageCount><abstractWordCount>93</abstractWordCount></qualityIndicators><title>Lymphedema-induced lymphangiosarcoma</title><pii><json:string>S0748-7983(95)90270-8</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Another facet of the Stewart-Treves syndrome</title><language><json:string>unknown</json:string></language><pages><first>456</first><last>463</last></pages></serie><host><title>European Journal of Surgical Oncology</title><language><json:string>unknown</json:string></language><publicationDate>1995</publicationDate><issn><json:string>0748-7983</json:string></issn><pii><json:string>S0748-7983(00)X0052-2</json:string></pii><volume>21</volume><issue>2</issue><pages><first>155</first><last>158</last></pages><genre><json:string>journal</json:string></genre></host><categories><wos><json:string>science</json:string><json:string>surgery</json:string><json:string>oncology</json:string></wos><scienceMetrix><json:string>health sciences</json:string><json:string>clinical medicine</json:string><json:string>oncology & carcinogenesis</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></inist></categories><publicationDate>1995</publicationDate><copyrightDate>1995</copyrightDate><doi><json:string>10.1016/S0748-7983(95)90270-8</json:string></doi><id>4502C1F68AAC9866DC15F684D509EDBAA88ECF0F</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/4502C1F68AAC9866DC15F684D509EDBAA88ECF0F/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/4502C1F68AAC9866DC15F684D509EDBAA88ECF0F/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/4502C1F68AAC9866DC15F684D509EDBAA88ECF0F/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Lymphedema-induced lymphangiosarcoma</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>ELSEVIER</publisher><availability><p>©1995 W.B. Saunders Company Limited</p></availability><date>1995</date></publicationStmt><notesStmt><note type="content">Section title: Original article</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Lymphedema-induced lymphangiosarcoma</title><author xml:id="author-0000"><persName><forename type="first">Arieke J.</forename><surname>Janse</surname></persName><affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Frits van</forename><surname>Coevorden</surname></persName><affiliation>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.</affiliation></author><author xml:id="author-0002"><persName><forename type="first">Hans</forename><surname>Peterse</surname></persName><affiliation>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation></author><author xml:id="author-0003"><persName><forename type="first">Ronald B.</forename><surname>Keus</surname></persName><affiliation>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation></author><author xml:id="author-0004"><persName><forename type="first">Johannes A. van</forename><surname>Dongen</surname></persName><affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation></author><idno type="istex">4502C1F68AAC9866DC15F684D509EDBAA88ECF0F</idno><idno type="DOI">10.1016/S0748-7983(95)90270-8</idno><idno type="PII">S0748-7983(95)90270-8</idno><idno type="ArticleID">95902708</idno></analytic><monogr><title level="j">European Journal of Surgical Oncology</title><title level="j" type="abbrev">YEJSO</title><idno type="pISSN">0748-7983</idno><idno type="PII">S0748-7983(00)X0052-2</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1995"></date><biblScope unit="volume">21</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="155">155</biblScope><biblScope unit="page" to="158">158</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1995</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><item><term>lymphangiosarcoma</term></item><item><term>angiosarcoma</term></item><item><term>Stewart-Treves syndrome</term></item><item><term>breast carcinoma</term></item><item><term>lymphedema</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1995">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/4502C1F68AAC9866DC15F684D509EDBAA88ECF0F/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>YEJSO</jid><aid>95902708</aid><ce:pii>S0748-7983(95)90270-8</ce:pii><ce:doi>10.1016/S0748-7983(95)90270-8</ce:doi><ce:copyright type="unknown" year="1995">W.B. Saunders Company Limited</ce:copyright></item-info><head><ce:dochead><ce:textfn>Original article</ce:textfn></ce:dochead><ce:title>Lymphedema-induced lymphangiosarcoma</ce:title><ce:author-group><ce:author><ce:given-name>Arieke J.</ce:given-name><ce:surname>Janse</ce:surname><ce:cross-ref refid="aff1"><ce:sup>a</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Frits van</ce:given-name><ce:surname>Coevorden</ce:surname><ce:cross-ref refid="cor1"><ce:sup>*</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Hans</ce:given-name><ce:surname>Peterse</ce:surname><ce:cross-ref refid="aff2"><ce:sup>*</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Ronald B.</ce:given-name><ce:surname>Keus</ce:surname><ce:cross-ref refid="aff3"><ce:sup>†</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Johannes A. van</ce:given-name><ce:surname>Dongen</ce:surname><ce:cross-ref refid="aff1"><ce:sup>a</ce:sup></ce:cross-ref></ce:author><ce:affiliation id="aff1"><ce:label>a</ce:label><ce:textfn>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</ce:textfn></ce:affiliation><ce:affiliation id="aff2"><ce:label>*</ce:label><ce:textfn>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</ce:textfn></ce:affiliation><ce:affiliation id="aff3"><ce:label>†</ce:label><ce:textfn>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</ce:textfn></ce:affiliation><ce:correspondence id="cor1"><ce:label>*</ce:label><ce:text>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.</ce:text></ce:correspondence></ce:author-group><ce:date-accepted day="20" month="10" year="1994"></ce:date-accepted><ce:abstract id="ab1" class="author" xml:lang="en"><ce:abstract-sec><ce:simple-para>A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:keywords xml:lang="en"><ce:keyword><ce:text>lymphangiosarcoma</ce:text></ce:keyword><ce:keyword><ce:text>angiosarcoma</ce:text></ce:keyword><ce:keyword><ce:text>Stewart-Treves syndrome</ce:text></ce:keyword><ce:keyword><ce:text>breast carcinoma</ce:text></ce:keyword><ce:keyword><ce:text>lymphedema</ce:text></ce:keyword></ce:keywords></head><tail><ce:bibliography><ce:section-title>References</ce:section-title><ce:bibliography-sec><ce:bib-reference id="bib1"><ce:label>1.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Stewart</ce:surname><ce:given-name>FM</ce:given-name></sb:author><sb:author><ce:surname>Treves</ce:surname><ce:given-name>N</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Lymphangiosarcoma in post-mastectomy lymphedema</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Cancer</sb:maintitle></sb:title><sb:volume-nr>1</sb:volume-nr></sb:series><sb:date>1948</sb:date></sb:issue><sb:pages><sb:first-page>64</sb:first-page><sb:last-page>81</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib2"><ce:label>2.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Fitzpatrick</ce:surname><ce:given-name>PJ</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Lymphangiosarcoma in breast cancer</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Can J Surg</sb:maintitle></sb:title><sb:volume-nr>12</sb:volume-nr></sb:series><sb:date>1969</sb:date></sb:issue><sb:pages><sb:first-page>172</sb:first-page><sb:last-page>177</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib3"><ce:label>3.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Shirger</ce:surname><ce:given-name>A</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Postoperative lymphedema: Etiology and diagnostic factors</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Med Clin North Am</sb:maintitle></sb:title><sb:volume-nr>46</sb:volume-nr></sb:series><sb:date>1962</sb:date></sb:issue><sb:pages><sb:first-page>1045</sb:first-page><sb:last-page>1050</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib4"><ce:label>4.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Barthal</ce:surname><ce:given-name>AH</ce:given-name></sb:author><sb:author><ce:surname>Pinsky</ce:surname><ce:given-name>CM</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Malignant melanoma appearing in a post-mastectomy lymphedematous arm: a novel association of double primary tumours</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>J Surg Oncol</sb:maintitle></sb:title><sb:volume-nr>30</sb:volume-nr></sb:series><sb:date>1985</sb:date></sb:issue><sb:pages><sb:first-page>16</sb:first-page><sb:last-page>18</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib5"><ce:label>5.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>d'Amore</ce:surname><ce:given-name>ESG</ce:given-name></sb:author><sb:author><ce:surname>Wick</ce:surname><ce:given-name>MR</ce:given-name></sb:author><sb:author><ce:surname>Geisinger</ce:surname><ce:given-name>KR</ce:given-name></sb:author><sb:author><ce:surname>Frizzera</ce:surname><ce:given-name>G</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Primary malignant lymphoma arising in postmastectomy lymphedema</sb:maintitle></sb:title></sb:contribution><sb:host><sb:edited-book><sb:title><sb:maintitle>Another facet of the Stewart-Treves syndrome</sb:maintitle></sb:title><sb:book-series><sb:series><sb:title><sb:maintitle>Am J Surg Pathol</sb:maintitle></sb:title><sb:volume-nr>14</sb:volume-nr></sb:series></sb:book-series><sb:date>1990</sb:date></sb:edited-book><sb:pages><sb:first-page>456</sb:first-page><sb:last-page>463</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib6"><ce:label>6.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>McWilliams</ce:surname><ce:given-name>LJ</ce:given-name></sb:author><sb:author><ce:surname>Harris</ce:surname><ce:given-name>M</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Histogenesis of post-mastectomy angiosarcoma-an ultrastructural study</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Histopathology</sb:maintitle></sb:title><sb:volume-nr>9</sb:volume-nr></sb:series><sb:date>1985</sb:date></sb:issue><sb:pages><sb:first-page>331</sb:first-page><sb:last-page>343</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib7"><ce:label>7.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Tomita</ce:surname><ce:given-name>K</ce:given-name></sb:author><sb:author><ce:surname>Yokogawa</ce:surname><ce:given-name>A</ce:given-name></sb:author><sb:author><ce:surname>Oda</ce:surname><ce:given-name>Y</ce:given-name></sb:author><sb:author><ce:surname>Terahata</ce:surname><ce:given-name>S</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Lymphangiosarcoma in postmastectomy lymphedema (Stewart-Treves syndrome): ultrastructural and immunologic characteristics</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>J Surg Oncol</sb:maintitle></sb:title><sb:volume-nr>38</sb:volume-nr></sb:series><sb:date>1988</sb:date></sb:issue><sb:pages><sb:first-page>275</sb:first-page><sb:last-page>282</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib8"><ce:label>8.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>McConnell</ce:surname><ce:given-name>AH</ce:given-name></sb:author><sb:author><ce:surname>Haslam</ce:surname><ce:given-name>P</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Angiosarcoma in post-mastectomy lymphedema: a report of five cases and a review of the literature</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Br J Surg</sb:maintitle></sb:title><sb:volume-nr>46</sb:volume-nr></sb:series><sb:date>1959</sb:date></sb:issue><sb:pages><sb:first-page>322</sb:first-page><sb:last-page>332</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib9"><ce:label>9.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Woodward</ce:surname><ce:given-name>AH</ce:given-name></sb:author><sb:author><ce:surname>Ivins</ce:surname><ce:given-name>JC</ce:given-name></sb:author><sb:author><ce:surname>Soule</ce:surname><ce:given-name>EH</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Lymphangiosarcoma arising in chronic lymphedematous extremities</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Cancer</sb:maintitle></sb:title><sb:volume-nr>30</sb:volume-nr></sb:series><sb:date>1972</sb:date></sb:issue><sb:pages><sb:first-page>562</sb:first-page><sb:last-page>572</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib10"><ce:label>10.</ce:label><sb:reference><sb:comment>Band VI/Heft</sb:comment><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Gregl</ce:surname><ce:given-name>A</ce:given-name></sb:author><sb:author><ce:surname>Schauer</ce:surname><ce:given-name>A</ce:given-name></sb:author><sb:author><ce:surname>Heyden</ce:surname><ce:given-name>VD</ce:given-name></sb:author><sb:author><ce:surname>Irrgang</ce:surname><ce:given-name>B</ce:given-name></sb:author><sb:author><ce:surname>Muschter</ce:surname><ce:given-name>R</ce:given-name></sb:author><sb:author><ce:surname>Oxen</ce:surname><ce:given-name>H</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Stewart-Treves-Syndrom am ödematösen Arm nach Brustkrebsoperation</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Lymphol</sb:maintitle></sb:title><sb:volume-nr>1</sb:volume-nr></sb:series><sb:date>1982</sb:date></sb:issue><sb:pages><sb:first-page>51</sb:first-page><sb:last-page>66</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib11"><ce:label>11.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Gregl</ce:surname><ce:given-name>A</ce:given-name></sb:author><sb:author><ce:surname>Pavic</ce:surname><ce:given-name>S</ce:given-name></sb:author><sb:author><ce:surname>Pavic</ce:surname><ce:given-name>Z</ce:given-name></sb:author><sb:author><ce:surname>Schauer</ce:surname><ce:given-name>A</ce:given-name></sb:author><sb:author><ce:surname>Wilke</ce:surname><ce:given-name>CH</ce:given-name></sb:author><sb:author><ce:surname>Zinn</ce:surname><ce:given-name>H</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Stewart-Treves-Syndrom am ödematösen Arm nach Brustkrebsoperation</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Lymphol</sb:maintitle></sb:title><sb:volume-nr>XII</sb:volume-nr></sb:series><sb:date>1988</sb:date></sb:issue><sb:pages><sb:first-page>66</sb:first-page><sb:last-page>83</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib12"><ce:label>12.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Brady</ce:surname><ce:given-name>MS</ce:given-name></sb:author><sb:author><ce:surname>Garfein</ce:surname><ce:given-name>CF</ce:given-name></sb:author><sb:author><ce:surname>Petrek</ce:surname><ce:given-name>JA</ce:given-name></sb:author><sb:author><ce:surname>Brennan</ce:surname><ce:given-name>MF</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Post-treatment sarcoma in breast cancer patients</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Ann Surg Oncol</sb:maintitle></sb:title><sb:volume-nr>1</sb:volume-nr></sb:series><sb:date>1994</sb:date></sb:issue><sb:pages><sb:first-page>66</sb:first-page><sb:last-page>72</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib13"><ce:label>13.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Amberger</ce:surname><ce:given-name>H</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Die Behandlung des Stewart-Treves-Syndrom</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Chirurg</sb:maintitle></sb:title><sb:volume-nr>54</sb:volume-nr></sb:series><sb:date>1983</sb:date></sb:issue><sb:pages><sb:first-page>487</sb:first-page><sb:last-page>489</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib14"><ce:label>14.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Martorell</ce:surname><ce:given-name>F</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Tumorigenic lymphedema</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Angiology</sb:maintitle></sb:title><sb:volume-nr>2</sb:volume-nr></sb:series><sb:date>1951</sb:date></sb:issue><sb:pages><sb:first-page>386</sb:first-page><sb:last-page>392</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib15"><ce:label>15.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Schreiber</ce:surname><ce:given-name>H</ce:given-name></sb:author><sb:author><ce:surname>Barry</ce:surname><ce:given-name>FM</ce:given-name></sb:author><sb:author><ce:surname>Russell</ce:surname><ce:given-name>WC</ce:given-name></sb:author><sb:author><ce:surname>Macon</ce:surname><ce:given-name>WL</ce:given-name></sb:author><sb:author><ce:surname>Ponsky</ce:surname><ce:given-name>JL</ce:given-name></sb:author><sb:author><ce:surname>Pories</ce:surname><ce:given-name>WJ</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Stewart-Treves syndrome: A lethal complication of postmastectomy lymphedema and regional immune deficiency</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Arch Surg</sb:maintitle></sb:title><sb:volume-nr>114</sb:volume-nr></sb:series><sb:date>1979</sb:date></sb:issue><sb:pages><sb:first-page>82</sb:first-page><sb:last-page>85</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib16"><ce:label>16.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Kaufmann</ce:surname><ce:given-name>T</ce:given-name></sb:author><sb:author><ce:surname>Chu</ce:surname><ce:given-name>F</ce:given-name></sb:author><sb:author><ce:surname>Kaufmann</ce:surname><ce:given-name>R</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Post-mastectomy lymphangiosarcoma (Stewart-Treves syndrome): report of two long term survivals</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Br J Radiol</sb:maintitle></sb:title><sb:volume-nr>64</sb:volume-nr></sb:series><sb:date>1991</sb:date></sb:issue><sb:pages><sb:first-page>857</sb:first-page><sb:last-page>860</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib17"><ce:label>17.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Disimone</ce:surname><ce:given-name>RN</ce:given-name></sb:author><sb:author><ce:surname>El-Mahdi</ce:surname><ce:given-name>AM</ce:given-name></sb:author><sb:author><ce:surname>Hazra</ce:surname><ce:given-name>T</ce:given-name></sb:author><sb:author><ce:surname>Lott</ce:surname><ce:given-name>S</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>The response of Stewart-Treves syndrome to radiotherapy</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Radiology</sb:maintitle></sb:title><sb:volume-nr>97</sb:volume-nr></sb:series><sb:date>1970</sb:date></sb:issue><sb:pages><sb:first-page>121</sb:first-page><sb:last-page>125</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib18"><ce:label>18.</ce:label><ce:other-ref><ce:textref>Gonzalez Gonzalez D. Personal communication.</ce:textref></ce:other-ref></ce:bib-reference><ce:bib-reference id="bib19"><ce:label>19.</ce:label><sb:reference><sb:contribution langtype="en"><sb:authors><sb:author><ce:surname>Yap</ce:surname><ce:given-name>BS</ce:given-name></sb:author><sb:author><ce:surname>Yap</ce:surname><ce:given-name>HY</ce:given-name></sb:author><sb:author><ce:surname>McBride</ce:surname><ce:given-name>CM</ce:given-name></sb:author><sb:author><ce:surname>Bodey</ce:surname><ce:given-name>GP</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Chemotherapy for postmastectomy lymphangiosarcoma</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Cancer</sb:maintitle></sb:title><sb:volume-nr>47</sb:volume-nr></sb:series><sb:date>1981</sb:date></sb:issue><sb:pages><sb:first-page>853</sb:first-page><sb:last-page>856</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>Lymphedema-induced lymphangiosarcoma</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Lymphedema-induced lymphangiosarcoma</title></titleInfo><name type="personal"><namePart type="given">Arieke J.</namePart><namePart type="family">Janse</namePart><affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Frits van</namePart><namePart type="family">Coevorden</namePart><affiliation>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Hans</namePart><namePart type="family">Peterse</namePart><affiliation>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ronald B.</namePart><namePart type="family">Keus</namePart><affiliation>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Johannes A. van</namePart><namePart type="family">Dongen</namePart><affiliation>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, The Netherlands</affiliation><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">1995</dateIssued><copyrightDate encoding="w3cdtf">1995</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">A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.</abstract><note type="content">Section title: Original article</note><subject lang="en"><topic>lymphangiosarcoma</topic><topic>angiosarcoma</topic><topic>Stewart-Treves syndrome</topic><topic>breast carcinoma</topic><topic>lymphedema</topic></subject><relatedItem type="host"><titleInfo><title>European Journal of Surgical Oncology</title></titleInfo><titleInfo type="abbreviated"><title>YEJSO</title></titleInfo><genre type="journal">journal</genre><originInfo><dateIssued encoding="w3cdtf">199504</dateIssued></originInfo><identifier type="ISSN">0748-7983</identifier><identifier type="PII">S0748-7983(00)X0052-2</identifier><part><date>199504</date><detail type="volume"><number>21</number><caption>vol.</caption></detail><detail type="issue"><number>2</number><caption>no.</caption></detail><extent unit="issue pages"><start>125</start><end>230</end></extent><extent unit="pages"><start>155</start><end>158</end></extent></part></relatedItem><identifier type="istex">4502C1F68AAC9866DC15F684D509EDBAA88ECF0F</identifier><identifier type="DOI">10.1016/S0748-7983(95)90270-8</identifier><identifier type="PII">S0748-7983(95)90270-8</identifier><identifier type="ArticleID">95902708</identifier><accessCondition type="use and reproduction" contentType="copyright">©1995 W.B. Saunders Company Limited</accessCondition><recordInfo><recordContentSource>ELSEVIER</recordContentSource><recordOrigin>W.B. Saunders Company Limited, ©1995</recordOrigin></recordInfo></mods></metadata></istex></record>Pour manipuler ce document sous Unix (Dilib)
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