Chronic lymphedema of filarial origin: a very rare etiology of cutaneous lymphangiosarcoma.
Identifieur interne : 001C26 ( PubMed/Checkpoint ); précédent : 001C25; suivant : 001C27Chronic lymphedema of filarial origin: a very rare etiology of cutaneous lymphangiosarcoma.
Auteurs : Shubhangi V. Agale [Inde] ; Wasif Ali Za Khan ; Karishma ChawlaniSource :
- Indian journal of dermatology [ 1998-3611 ] ; 2013.
Abstract
Lymphedema-associated angiosarcoma also known as lymphangiosarcoma is the commonest type of cutaneous angiosarcoma. Post-mastectomy lymphedema is the most frequent cause, while chronic filarial lymphedema is one of the most uncommon etiology for development of lymphangiosarcoma. We report a case of a 50 year old male suffering from chronic filarial lymphedema of right lower extremity, presented with brownish nodules on the right leg, which were diagnosed histopathologically as lymphangiosarcoma.
DOI: 10.4103/0019-5154.105315
PubMed: 23372219
Affiliations:
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<front><div type="abstract" xml:lang="en">Lymphedema-associated angiosarcoma also known as lymphangiosarcoma is the commonest type of cutaneous angiosarcoma. Post-mastectomy lymphedema is the most frequent cause, while chronic filarial lymphedema is one of the most uncommon etiology for development of lymphangiosarcoma. We report a case of a 50 year old male suffering from chronic filarial lymphedema of right lower extremity, presented with brownish nodules on the right leg, which were diagnosed histopathologically as lymphangiosarcoma.</div>
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<Abstract><AbstractText>Lymphedema-associated angiosarcoma also known as lymphangiosarcoma is the commonest type of cutaneous angiosarcoma. Post-mastectomy lymphedema is the most frequent cause, while chronic filarial lymphedema is one of the most uncommon etiology for development of lymphangiosarcoma. We report a case of a 50 year old male suffering from chronic filarial lymphedema of right lower extremity, presented with brownish nodules on the right leg, which were diagnosed histopathologically as lymphangiosarcoma.</AbstractText>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Indian J Cancer. 1977 Jun;14(2):176-8</RefSource>
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