Angiosarcoma arising in a lymphedematous abdominal pannus with histologic features reminiscent of Kaposi's sarcoma: report of a case and review of the literature.
Identifieur interne : 002235 ( Ncbi/Curation ); précédent : 002234; suivant : 002236Angiosarcoma arising in a lymphedematous abdominal pannus with histologic features reminiscent of Kaposi's sarcoma: report of a case and review of the literature.
Auteurs : James M. Shehan [États-Unis] ; Iftikhar AhmedSource :
- International journal of dermatology [ 0011-9059 ] ; 2006.
Descripteurs français
- KwdFr :
- Abdomen (anatomopathologie), Diagnostic différentiel, Femelle, Humains, Hémangiosarcome (diagnostic), Hémangiosarcome (secondaire), Hémangiosarcome (traitement médicamenteux), Issue fatale, Obésité morbide, Oedème, Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique), Sarcome de Kaposi (diagnostic), Sujet âgé, Sujet âgé de 80 ans ou plus, Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (diagnostic), Tumeurs cutanées (traitement médicamenteux), Tumeurs du poumon (diagnostic), Tumeurs du poumon (secondaire), Tumeurs du poumon (traitement médicamenteux).
- MESH :
- anatomopathologie : Abdomen, Tumeurs cutanées.
- diagnostic : Hémangiosarcome, Sarcome de Kaposi, Tumeurs cutanées, Tumeurs du poumon.
- secondaire : Hémangiosarcome, Tumeurs du poumon.
- traitement médicamenteux : Hémangiosarcome, Tumeurs cutanées, Tumeurs du poumon.
- usage thérapeutique : Protocoles de polychimiothérapie antinéoplasique.
- Diagnostic différentiel, Femelle, Humains, Issue fatale, Obésité morbide, Oedème, Sujet âgé, Sujet âgé de 80 ans ou plus.
English descriptors
- KwdEn :
- Abdomen (pathology), Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols (therapeutic use), Diagnosis, Differential, Edema, Fatal Outcome, Female, Hemangiosarcoma (diagnosis), Hemangiosarcoma (drug therapy), Hemangiosarcoma (secondary), Humans, Lung Neoplasms (diagnosis), Lung Neoplasms (drug therapy), Lung Neoplasms (secondary), Obesity, Morbid, Sarcoma, Kaposi (diagnosis), Skin Neoplasms (diagnosis), Skin Neoplasms (drug therapy), Skin Neoplasms (pathology).
- MESH :
- diagnosis : Hemangiosarcoma, Lung Neoplasms, Sarcoma, Kaposi, Skin Neoplasms.
- drug therapy : Hemangiosarcoma, Lung Neoplasms, Skin Neoplasms.
- pathology : Abdomen, Skin Neoplasms.
- secondary : Hemangiosarcoma, Lung Neoplasms.
- therapeutic use : Antineoplastic Combined Chemotherapy Protocols.
- Aged, Aged, 80 and over, Diagnosis, Differential, Edema, Fatal Outcome, Female, Humans, Obesity, Morbid.
Abstract
Despite common endothelial origins, angiosarcoma and Kaposi's sarcoma are clinically and histologically distinct vascular proliferations. The development of angiosarcoma in a chronically edematous abdominal pannus is extremely uncommon. Similarly, tumors with the combined histologic features of angiosarcoma and Kaposi's sarcoma have rarely been described.
DOI: 10.1111/j.1365-4632.2004.02560.x
PubMed: 16700780
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pubmed:16700780Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abdomen (pathology)</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Antineoplastic Combined Chemotherapy Protocols (therapeutic use)</term>
<term>Diagnosis, Differential</term>
<term>Edema</term>
<term>Fatal Outcome</term>
<term>Female</term>
<term>Hemangiosarcoma (diagnosis)</term>
<term>Hemangiosarcoma (drug therapy)</term>
<term>Hemangiosarcoma (secondary)</term>
<term>Humans</term>
<term>Lung Neoplasms (diagnosis)</term>
<term>Lung Neoplasms (drug therapy)</term>
<term>Lung Neoplasms (secondary)</term>
<term>Obesity, Morbid</term>
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<term>Skin Neoplasms (diagnosis)</term>
<term>Skin Neoplasms (drug therapy)</term>
<term>Skin Neoplasms (pathology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Abdomen (anatomopathologie)</term>
<term>Diagnostic différentiel</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémangiosarcome (diagnostic)</term>
<term>Hémangiosarcome (secondaire)</term>
<term>Hémangiosarcome (traitement médicamenteux)</term>
<term>Issue fatale</term>
<term>Obésité morbide</term>
<term>Oedème</term>
<term>Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique)</term>
<term>Sarcome de Kaposi (diagnostic)</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Tumeurs cutanées (anatomopathologie)</term>
<term>Tumeurs cutanées (diagnostic)</term>
<term>Tumeurs cutanées (traitement médicamenteux)</term>
<term>Tumeurs du poumon (diagnostic)</term>
<term>Tumeurs du poumon (secondaire)</term>
<term>Tumeurs du poumon (traitement médicamenteux)</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Abdomen</term>
<term>Tumeurs cutanées</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Hemangiosarcoma</term>
<term>Lung Neoplasms</term>
<term>Sarcoma, Kaposi</term>
<term>Skin Neoplasms</term>
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<term>Sarcome de Kaposi</term>
<term>Tumeurs cutanées</term>
<term>Tumeurs du poumon</term>
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<term>Lung Neoplasms</term>
<term>Skin Neoplasms</term>
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<term>Skin Neoplasms</term>
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<term>Tumeurs du poumon</term>
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<term>Lung Neoplasms</term>
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<keywords scheme="MESH" qualifier="therapeutic use" xml:lang="en"><term>Antineoplastic Combined Chemotherapy Protocols</term>
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<term>Tumeurs cutanées</term>
<term>Tumeurs du poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Protocoles de polychimiothérapie antinéoplasique</term>
</keywords>
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<term>Aged, 80 and over</term>
<term>Diagnosis, Differential</term>
<term>Edema</term>
<term>Fatal Outcome</term>
<term>Female</term>
<term>Humans</term>
<term>Obesity, Morbid</term>
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<term>Femelle</term>
<term>Humains</term>
<term>Issue fatale</term>
<term>Obésité morbide</term>
<term>Oedème</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
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<front><div type="abstract" xml:lang="en">Despite common endothelial origins, angiosarcoma and Kaposi's sarcoma are clinically and histologically distinct vascular proliferations. The development of angiosarcoma in a chronically edematous abdominal pannus is extremely uncommon. Similarly, tumors with the combined histologic features of angiosarcoma and Kaposi's sarcoma have rarely been described.</div>
</front>
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