1981
DOI: 10.1111/j.1524-4725.1981.tb00632.x
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Lymphangiosarcoma after Filarial Infection

Abstract: A case of lymphangiosarcoma of a lower extremity is described in a patient with chronic lymphedema of that leg from a filarial infection in childhood. Histologically, the neoplasm resembled lymphangiosarcomas that arise in arms that become lymphedematous after mastectomies, but was different in that it also contained areas of calcification consistent with prior filarial infection. Calcifications were also present in muscle uninvolved by the lymphangiosarcoma of this case. The prolonged survival of this patient… Show more

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Cited by 33 publications
(16 citation statements)
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“…3,4 Other factors with an adverse impact on prognosis are older age, tumor necrosis, and epitheloid features. 5 Tumors can arise either de novo (primary AS, pAS) or as secondary conditions in patients with long standing lymphedema 6,7 or after irradiation 8 (secondary AS; sAS), especially in female patients irradiated for breast cancer. In fact, sAS of the breast is by far the most frequent radiation-induced sarcoma in women treated with radiation therapy as part of their initial treatment, 9 with a more than 1000-fold increased relative risk 10 as compared with the general population.…”
mentioning
confidence: 99%
“…3,4 Other factors with an adverse impact on prognosis are older age, tumor necrosis, and epitheloid features. 5 Tumors can arise either de novo (primary AS, pAS) or as secondary conditions in patients with long standing lymphedema 6,7 or after irradiation 8 (secondary AS; sAS), especially in female patients irradiated for breast cancer. In fact, sAS of the breast is by far the most frequent radiation-induced sarcoma in women treated with radiation therapy as part of their initial treatment, 9 with a more than 1000-fold increased relative risk 10 as compared with the general population.…”
mentioning
confidence: 99%
“…L'angiosarcome développé dans un lymphoedème d'une autre origine, congé nital ou acquis [3,11,18,22,25] doit échap per à la terminologie de syndrome de Ste wart-Treves. La distinction est plus aisée avec l'angiosarcome proprement dit [2,17] et l'hémangioendothéliome malin de la face chez la personne âgée [9,17].…”
Section: Resultsunclassified
“…Muller et al [3] mentioned three cases. Sordillo et al [4], Sinclair et al [5], Hallel-Halevy et al [6], Komorowski et al [7] have also reported cases of angiosarcoma in long-standing elephantiasis.…”
Section: Discussionmentioning
confidence: 98%