Vascular proliferations of the breast
Identifieur interne : 004734 ( Istex/Corpus ); précédent : 004733; suivant : 004735Vascular proliferations of the breast
Auteurs : C. Brodie ; E. ProvenzanoSource :
- Histopathology [ 0309-0167 ] ; 2008-01.
Abstract
Vascular proliferations of the breast are uncommon but potentially diagnostically challenging lesions. Clinically apparent processes are more likely to be malignant; however, a range of benign entities which must be differentiated from angiosarcoma also exists. This review discusses first, breast lesions of apparent vascular origin, then benign and histologically bland perilobular, cavernous and capillary haemangiomas. Subsequently, more diagnostically challenging, atypical haemangiomas, papillary endothelial hyperplasia, angiomatosis and angiolymphoid hyperplasia with eosinophilia (epithelioid haemangioma) are considered. In addition, lesions with low‐grade malignant potential such as haemangiopericytomas and epithelioid haemangioendotheliomas may rarely present in the breast. However, primary angiosarcomas and radiation‐associated vascular lesions are reviewed in depth, as these entities are of greatest clinical and pathological significance.
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DOI: 10.1111/j.1365-2559.2007.02892.x
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Provenzano</name><affiliation><mods:affiliation>Department of Histopathology, University College Hospital, Galway, Ireland, and Addenbrooke’s Hospital, Cambridge, UK</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Histopathology</title><title level="j" type="alt">HISTOPATHOLOGY</title><idno type="ISSN">0309-0167</idno><idno type="eISSN">1365-2559</idno><imprint><biblScope unit="vol">52</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="30">30</biblScope><biblScope unit="page" to="44">44</biblScope><biblScope unit="page-count">15</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2008-01">2008-01</date></imprint><idno type="ISSN">0309-0167</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0309-0167</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Vascular proliferations of the breast are uncommon but potentially diagnostically challenging lesions. 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However, primary angiosarcomas and radiation‐associated vascular lesions are reviewed in depth, as these entities are of greatest clinical and pathological significance.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">angiomatosis</term><term xml:id="k2">angiosarcoma</term><term xml:id="k3">breast</term><term xml:id="k4">epithelioid haemangioendothelioma</term><term xml:id="k5">epithelioid haemangioma</term><term xml:id="k6">haemangioma</term><term xml:id="k7">pseudoangiomatous stromal hyperplasia</term><term xml:id="k8">vascular lesions</term></keywords><classCode scheme="tocHeading1">Reviews</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/970F72F3009EF8FCA0511F0AFA760166EFF86241/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>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1365-2559</doi><issn type="print">0309-0167</issn><issn type="electronic">1365-2559</issn><idGroup><id type="product" value="HIS"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="HISTOPATHOLOGY">Histopathology</title></titleGroup></publicationMeta><publicationMeta level="part" position="01001"><doi origin="wiley">10.1111/his.2008.52.issue-1</doi><numberingGroup><numbering type="journalVolume" number="52">52</numbering><numbering type="journalIssue" number="1">1</numbering></numberingGroup><coverDate startDate="2008-01">January 2008</coverDate></publicationMeta><publicationMeta level="unit" type="reviewArticle" position="5" status="forIssue"><doi origin="wiley">10.1111/j.1365-2559.2007.02892.x</doi><idGroup><id type="unit" value="HIS2892"></id></idGroup><countGroup><count type="pageTotal" number="15"></count></countGroup><titleGroup><title type="tocHeading1">Reviews</title></titleGroup><eventGroup><event type="firstOnline" date="2007-12-13"></event><event type="publishedOnlineFinalForm" date="2007-12-13"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-06"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-27"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-23"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="30">30</numbering><numbering type="pageLast" number="44">44</numbering></numberingGroup><correspondenceTo>C Brodie, Department of Histopathology, University College Hospital, Newcastle Road, Galway, Ireland.
e‐mail: <email>cmbrodie@gmail.com</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:HIS.HIS2892.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="6"></count><count type="tableTotal" number="2"></count></countGroup><titleGroup><title type="main">Vascular proliferations of the breast</title><title type="shortAuthors"><i>C Brodie & E Provenzano</i></title><title type="short"><i>Vascular proliferations</i></title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>C</givenNames><familyName>Brodie</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>E</givenNames><familyName>Provenzano</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="GB"><unparsedAffiliation>Department of Histopathology, University College Hospital, Galway, Ireland, and Addenbrooke’s Hospital, Cambridge, UK</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">angiomatosis</keyword><keyword xml:id="k2">angiosarcoma</keyword><keyword xml:id="k3">breast</keyword><keyword xml:id="k4">epithelioid haemangioendothelioma</keyword><keyword xml:id="k5">epithelioid haemangioma</keyword><keyword xml:id="k6">haemangioma</keyword><keyword xml:id="k7">pseudoangiomatous stromal hyperplasia</keyword><keyword xml:id="k8">vascular lesions</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><!--
Brodie C & Provenzano E
(2008) Histopathology52, 30–44Vascular proliferations of the breast
--><p>Vascular proliferations of the breast are uncommon but potentially diagnostically challenging lesions. Clinically apparent processes are more likely to be malignant; however, a range of benign entities which must be differentiated from angiosarcoma also exists. This review discusses first, breast lesions of apparent vascular origin, then benign and histologically bland perilobular, cavernous and capillary haemangiomas. Subsequently, more diagnostically challenging, atypical haemangiomas, papillary endothelial hyperplasia, angiomatosis and angiolymphoid hyperplasia with eosinophilia (epithelioid haemangioma) are considered. In addition, lesions with low‐grade malignant potential such as haemangiopericytomas and epithelioid haemangioendotheliomas may rarely present in the breast. However, primary angiosarcomas and radiation‐associated vascular lesions are reviewed in depth, as these entities are of greatest clinical and pathological significance.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Vascular proliferations of the breast</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Vascular proliferations</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Vascular proliferations of the breast</title></titleInfo><name type="personal"><namePart type="given">C</namePart><namePart type="family">Brodie</namePart><affiliation>Department of Histopathology, University College Hospital, Galway, Ireland, and Addenbrooke’s Hospital, Cambridge, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E</namePart><namePart type="family">Provenzano</namePart><affiliation>Department of Histopathology, University College Hospital, Galway, Ireland, and Addenbrooke’s Hospital, Cambridge, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="reviewArticle"></genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2008-01</dateIssued><copyrightDate encoding="w3cdtf">2008</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">2</extent></physicalDescription><abstract lang="en">Vascular proliferations of the breast are uncommon but potentially diagnostically challenging lesions. Clinically apparent processes are more likely to be malignant; however, a range of benign entities which must be differentiated from angiosarcoma also exists. This review discusses first, breast lesions of apparent vascular origin, then benign and histologically bland perilobular, cavernous and capillary haemangiomas. Subsequently, more diagnostically challenging, atypical haemangiomas, papillary endothelial hyperplasia, angiomatosis and angiolymphoid hyperplasia with eosinophilia (epithelioid haemangioma) are considered. In addition, lesions with low‐grade malignant potential such as haemangiopericytomas and epithelioid haemangioendotheliomas may rarely present in the breast. However, primary angiosarcomas and radiation‐associated vascular lesions are reviewed in depth, as these entities are of greatest clinical and pathological significance.</abstract><subject lang="en"><genre>keywords</genre><topic>angiomatosis</topic><topic>angiosarcoma</topic><topic>breast</topic><topic>epithelioid haemangioendothelioma</topic><topic>epithelioid haemangioma</topic><topic>haemangioma</topic><topic>pseudoangiomatous stromal hyperplasia</topic><topic>vascular lesions</topic></subject><relatedItem type="host"><titleInfo><title>Histopathology</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0309-0167</identifier><identifier type="eISSN">1365-2559</identifier><identifier type="DOI">10.1111/(ISSN)1365-2559</identifier><identifier type="PublisherID">HIS</identifier><part><date>2008</date><detail type="volume"><caption>vol.</caption><number>52</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>30</start><end>44</end><total>15</total></extent></part></relatedItem><identifier type="istex">970F72F3009EF8FCA0511F0AFA760166EFF86241</identifier><identifier type="DOI">10.1111/j.1365-2559.2007.02892.x</identifier><identifier type="ArticleID">HIS2892</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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