Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease)--diagnostic beacons and a review of the literature.
Identifieur interne : 005763 ( PubMed/Curation ); précédent : 005762; suivant : 005764Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease)--diagnostic beacons and a review of the literature.
Auteurs : T W Offori [Royaume-Uni] ; C C Platt ; M. Stephens ; G B HopkinsonSource :
- Clinical and experimental dermatology [ 0307-6938 ] ; 1993.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Hémangiosarcome, Tumeurs cutanées.
- génétique : Lymphoedème.
- étiologie : Hémangiosarcome, Tumeurs cutanées.
- Adulte, Famille, Femelle, Humains, Jambe, Lymphoedème.
English descriptors
- KwdEn :
- MESH :
- complications : Lymphedema.
- congenital : Lymphedema.
- etiology : Hemangiosarcoma, Skin Neoplasms.
- genetics : Lymphedema.
- pathology : Hemangiosarcoma, Skin Neoplasms.
- Adult, Family, Female, Humans, Leg.
Abstract
In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses should act as a diagnostic beacon warning of dangers. A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. A review of cases of angiosarcoma complicating congenital hereditary and non-hereditary lymphoedema is also presented.
PubMed: 8482001
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A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. A review of cases of angiosarcoma complicating congenital hereditary and non-hereditary lymphoedema is also presented.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">8482001</PMID><DateCreated><Year>1993</Year><Month>06</Month><Day>03</Day></DateCreated><DateCompleted><Year>1993</Year><Month>06</Month><Day>03</Day></DateCompleted><DateRevised><Year>2005</Year><Month>11</Month><Day>16</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0307-6938</ISSN><JournalIssue CitedMedium="Print"><Volume>18</Volume><Issue>2</Issue><PubDate><Year>1993</Year><Month>Mar</Month></PubDate></JournalIssue><Title>Clinical and experimental dermatology</Title><ISOAbbreviation>Clin. Exp. Dermatol.</ISOAbbreviation></Journal><ArticleTitle>Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease)--diagnostic beacons and a review of the literature.</ArticleTitle><Pagination><MedlinePgn>174-7</MedlinePgn></Pagination><Abstract><AbstractText>In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses should act as a diagnostic beacon warning of dangers. A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. 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