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肾移植受者中表现为噬血细胞综合征的播散性血管肉瘤。

Disseminated angiosarcoma presenting as a hemophagocytic syndrome in a renal allograft recipient.

作者信息

Dargent J L, Vermylen P, Abramowicz D, Lespagnard L, Cochaux P, Capel P, Velu T, Vereerstraeten P, Haot J, De Wolf-Peeters C

机构信息

Department of Pathology, ULB-Erasme Hospital, Brussels, Belgium.

出版信息

Transpl Int. 1997;10(1):61-4. doi: 10.1007/BF02044344.

Abstract

A case of angiosarcoma arising in the setting of transplantation is reported. This rare and malignant tumor of the endothelial system is seldom observed in allograft recipients, with only seven cases having been previously reported. What is interesting about the present observation is that the tumor is thought to have developed in the vicinity of a Dacron graft and that it showed prominent erythrophagocyte-like activity. This activity was associated with a particular clinical syndrome that shared some attributes with infection-associated hemophagocytic syndrome.

摘要

本文报告了一例发生于移植背景下的血管肉瘤病例。这种内皮系统的罕见恶性肿瘤在同种异体移植受者中很少见,此前仅报告过7例。本次观察中有趣的是,该肿瘤被认为是在涤纶移植物附近发生的,并且表现出显著的类红细胞吞噬活性。这种活性与一种特殊的临床综合征相关,该综合征与感染相关噬血细胞综合征有一些共同特征。

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