Lymphangiosarcoma in postmastectomy lymphedema (Stewart‐Treves syndrome): Ultrastructural and immunohistologic characteristics
Identifieur interne : 000F99 ( Istex/Corpus ); précédent : 000F98; suivant : 001000Lymphangiosarcoma in postmastectomy lymphedema (Stewart‐Treves syndrome): Ultrastructural and immunohistologic characteristics
Auteurs : Katsuro Tomita ; Akio Yokogawa ; Yoshio Oda ; Shintaro TerahataSource :
- Journal of Surgical Oncology [ 0022-4790 ] ; 1988-08.
Abstract
Two cases of lymphangiosarcoma arising in a chronic lymphedematous extremity following mastectomy (Stewart‐Treves syndrome) were reported with not only standard histology, but also special study on the ultrastructure and immunohistology. These cancers developed as a result of chronic lymphedema of the involved limb following mastectomy 15 and 16 years ago, respectively, for breast carcinoma. Immunohistologic and electron microscopic examinations proved that this tumor originates in the vascular endotheliocytes, even though they are clinically chronic lesions apparently derived from the lymphatic vessels. This sarcoma develops multicentrically in an edematous arm and spreads out rapidly, so prognosis is quite discouraging in those patients. They need to be radically surgically treated without hesitation; hence, amputation, not limb‐saving surgery, should be indicated.
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DOI: 10.1002/jso.2930380415
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ISTEX:227B5A4592B08A1FB6E5263117420C1FD755518ALe document en format XML
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These cancers developed as a result of chronic lymphedema of the involved limb following mastectomy 15 and 16 years ago, respectively, for breast carcinoma. Immunohistologic and electron microscopic examinations proved that this tumor originates in the vascular endotheliocytes, even though they are clinically chronic lesions apparently derived from the lymphatic vessels. This sarcoma develops multicentrically in an edematous arm and spreads out rapidly, so prognosis is quite discouraging in those patients. They need to be radically surgically treated without hesitation; hence, amputation, not limb‐saving surgery, should be indicated.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>lymphangiosarcoma</json:string><json:string>lymphedema</json:string><json:string>postmastectomy</json:string><json:string>mastectomy</json:string><json:string>tumor cells</json:string><json:string>nodule</json:string><json:string>chronic lymphedema</json:string><json:string>postmastectomy lymphangiosarcoma</json:string><json:string>amputation</json:string><json:string>resection</json:string><json:string>angiosarcoma</json:string><json:string>haslam</json:string><json:string>radical mastectomy</json:string><json:string>sordillo</json:string><json:string>wide resection</json:string><json:string>ultrastructural</json:string><json:string>treves</json:string><json:string>breast carcinoma</json:string><json:string>immunohistologic</json:string><json:string>tomita</json:string><json:string>breast cancer</json:string><json:string>subcutaneous</json:string><json:string>endothelium</json:string><json:string>lumen</json:string><json:string>subcutaneous tissue</json:string><json:string>multiple nodules</json:string><json:string>vascular endotheliocytes</json:string><json:string>vascular endothelium</json:string><json:string>radiation therapy</json:string><json:string>edematous</json:string><json:string>carcinoma</json:string><json:string>recurrence</json:string><json:string>syndrome</json:string><json:string>upper extremity</json:string><json:string>factor viii</json:string><json:string>basement membrane</json:string><json:string>specific marker</json:string><json:string>kanazawa university school</json:string><json:string>orthopaedic surgery</json:string><json:string>histopathologic findings</json:string><json:string>silver staining</json:string><json:string>early amputation</json:string><json:string>reticular fibers</json:string></teeft></keywords><author><json:item><name>Katsuro Tomita MD, PhD</name><affiliations><json:string>Departments of Orthopaedic Surgery, Kanazawa University School of Medicine, Japan</json:string><json:string>Department of Orthopaedic Surgery, Kanazawa University School of Medicine, Takaramachi 13‐1, Kanazawa, 920, Japan</json:string></affiliations></json:item><json:item><name>Akio Yokogawa MD</name><affiliations><json:string>Departments of Orthopaedic Surgery, Kanazawa University School of Medicine, Japan</json:string></affiliations></json:item><json:item><name>Yoshio Oda MD</name><affiliations><json:string>Departments of Pathology, Kanazawa University School of Medicine, Japan</json:string></affiliations></json:item><json:item><name>Shintaro Terahata MD</name><affiliations><json:string>Departments of Pathology, Kanazawa University School of Medicine, Japan</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>breast carcinoma</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>lymphedema</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>amputation</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>immunohistology</value></json:item></subject><articleId><json:string>JSO2930380415</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Two cases of lymphangiosarcoma arising in a chronic lymphedematous extremity following mastectomy (Stewart‐Treves syndrome) were reported with not only standard histology, but also special study on the ultrastructure and immunohistology. 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xml:id="author-0000" role="corresp"><persName><forename type="first">Katsuro</forename><surname>Tomita</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Departments of Orthopaedic Surgery, Kanazawa University School of Medicine, Japan<address><country key="JP"></country></address></affiliation><affiliation>Department of Orthopaedic Surgery, Kanazawa University School of Medicine, Takaramachi 13‐1, Kanazawa, 920, Japan</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Akio</forename><surname>Yokogawa</surname><roleName type="degree">MD</roleName></persName><affiliation>Departments of Orthopaedic Surgery, Kanazawa University School of Medicine, Japan<address><country key="JP"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Yoshio</forename><surname>Oda</surname><roleName type="degree">MD</roleName></persName><affiliation>Departments of Pathology, Kanazawa University School of Medicine, Japan<address><country key="JP"></country></address></affiliation></author><author xml:id="author-0003"><persName><forename type="first">Shintaro</forename><surname>Terahata</surname><roleName type="degree">MD</roleName></persName><affiliation>Departments of Pathology, Kanazawa University School of Medicine, Japan<address><country key="JP"></country></address></affiliation></author><idno type="istex">227B5A4592B08A1FB6E5263117420C1FD755518A</idno><idno type="DOI">10.1002/jso.2930380415</idno><idno type="unit">JSO2930380415</idno><idno type="toTypesetVersion">file:JSO.JSO2930380415.pdf</idno></analytic><monogr><title level="j" type="main">Journal of Surgical Oncology</title><title level="j" type="alt">JOURNAL OF SURGICAL ONCOLOGY</title><idno type="pISSN">0022-4790</idno><idno type="eISSN">1096-9098</idno><idno type="book-DOI">10.1002/(ISSN)1096-9098</idno><idno type="book-part-DOI">10.1002/jso.v38:4</idno><idno type="product">JSO</idno><imprint><biblScope unit="vol">38</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="275">275</biblScope><biblScope unit="page" to="282">282</biblScope><biblScope unit="page-count">8</biblScope><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>New York</pubPlace><date type="published" when="1988-08"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p>Two cases of lymphangiosarcoma arising in a chronic lymphedematous extremity following mastectomy (Stewart‐Treves syndrome) were reported with not only standard histology, but also special study on the ultrastructure and immunohistology. These cancers developed as a result of chronic lymphedema of the involved limb following mastectomy 15 and 16 years ago, respectively, for breast carcinoma. Immunohistologic and electron microscopic examinations proved that this tumor originates in the vascular endotheliocytes, even though they are clinically chronic lesions apparently derived from the lymphatic vessels. This sarcoma develops multicentrically in an edematous arm and spreads out rapidly, so prognosis is quite discouraging in those patients. They need to be radically surgically treated without hesitation; hence, amputation, not limb‐saving surgery, should be indicated.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="kwd1">lymphangiosarcoma</term><term xml:id="kwd2">breast carcinoma</term><term xml:id="kwd3">lymphedema</term><term xml:id="kwd4">amputation</term><term xml:id="kwd5">immunohistology</term></keywords><classCode scheme="articleCategory">Article</classCode><classCode scheme="tocHeading1">Articles</classCode></textClass><langUsage><language ident="EN"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/227B5A4592B08A1FB6E5263117420C1FD755518A/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>New York</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1096-9098</doi><issn type="print">0022-4790</issn><issn type="electronic">1096-9098</issn><idGroup><id type="product" value="JSO"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="JOURNAL OF SURGICAL ONCOLOGY">Journal of Surgical Oncology</title><title type="short">J. 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These cancers developed as a result of chronic lymphedema of the involved limb following mastectomy 15 and 16 years ago, respectively, for breast carcinoma. Immunohistologic and electron microscopic examinations proved that this tumor originates in the vascular endotheliocytes, even though they are clinically chronic lesions apparently derived from the lymphatic vessels. This sarcoma develops multicentrically in an edematous arm and spreads out rapidly, so prognosis is quite discouraging in those patients. They need to be radically surgically treated without hesitation; hence, amputation, not limb‐saving surgery, should be indicated.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Lymphangiosarcoma in postmastectomy lymphedema (Stewart‐Treves syndrome): Ultrastructural and immunohistologic characteristics</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Lymphangiosarcoma in Postmastectomy Lymphedema (Stewart‐Treves Syndrome)</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Lymphangiosarcoma in postmastectomy lymphedema (Stewart‐Treves syndrome): Ultrastructural and immunohistologic characteristics</title></titleInfo><name type="personal"><namePart type="given">Katsuro</namePart><namePart type="family">Tomita</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Departments of Orthopaedic Surgery, Kanazawa University School of Medicine, Japan</affiliation><affiliation>Department of Orthopaedic Surgery, Kanazawa University School of Medicine, Takaramachi 13‐1, Kanazawa, 920, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role><description>Associate Professor</description></name><name type="personal"><namePart type="given">Akio</namePart><namePart type="family">Yokogawa</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Orthopaedic Surgery, Kanazawa University School of Medicine, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Yoshio</namePart><namePart type="family">Oda</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Pathology, Kanazawa University School of Medicine, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Shintaro</namePart><namePart type="family">Terahata</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Pathology, Kanazawa University School of Medicine, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">1988-08</dateIssued><dateValid encoding="w3cdtf">1987-09-14</dateValid><copyrightDate encoding="w3cdtf">1988</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">6</extent><extent unit="tables">1</extent><extent unit="references">17</extent></physicalDescription><abstract lang="en">Two cases of lymphangiosarcoma arising in a chronic lymphedematous extremity following mastectomy (Stewart‐Treves syndrome) were reported with not only standard histology, but also special study on the ultrastructure and immunohistology. These cancers developed as a result of chronic lymphedema of the involved limb following mastectomy 15 and 16 years ago, respectively, for breast carcinoma. Immunohistologic and electron microscopic examinations proved that this tumor originates in the vascular endotheliocytes, even though they are clinically chronic lesions apparently derived from the lymphatic vessels. This sarcoma develops multicentrically in an edematous arm and spreads out rapidly, so prognosis is quite discouraging in those patients. They need to be radically surgically treated without hesitation; hence, amputation, not limb‐saving surgery, should be indicated.</abstract><subject lang="en"><genre>keywords</genre><topic>lymphangiosarcoma</topic><topic>breast carcinoma</topic><topic>lymphedema</topic><topic>amputation</topic><topic>immunohistology</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Surgical Oncology</title></titleInfo><titleInfo type="abbreviated"><title>J. Surg. Oncol.</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Article</topic></subject><identifier type="ISSN">0022-4790</identifier><identifier type="eISSN">1096-9098</identifier><identifier type="DOI">10.1002/(ISSN)1096-9098</identifier><identifier type="PublisherID">JSO</identifier><part><date>1988</date><detail type="volume"><caption>vol.</caption><number>38</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>275</start><end>282</end><total>8</total></extent></part></relatedItem><identifier type="istex">227B5A4592B08A1FB6E5263117420C1FD755518A</identifier><identifier type="DOI">10.1002/jso.2930380415</identifier><identifier type="ArticleID">JSO2930380415</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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