Wijermans P W, van Groningen K, van Royen E A, Bruijn J A
Department of Hematology, Municipal Hospital Leyenburg, The Hague, The Netherlands.
Ann Hematol. 1994 Jun;68(6):307-10. doi: 10.1007/BF01695038.
A patient is described with a rapidly progressive Kaposi's sarcoma following immunosuppressive therapy with fludarabine monophosphate (FAMP) for chronic lymphocytic leukemia. The development of this tumor was accompanied by progressive thrombocytopenia, due to trapping of the platelets in the Kaposi sarcoma, without signs of consumptive coagulopathy or microangiopathic hemolytic anemia. This sequestration process might be caused by the abnormal structure of the tumoral vessels, leading to exposure of subendothelial structures like collagen, von Willebrand's factor, and tenascin to the vessel lumen. A severe immunosuppression due to the lymphocytotoxic effect of FAMP on several T-cell subpopulations was seen. This case confirms the importance of immunosuppression as a co-factor in the development of Kaposi's sarcoma also in HIV-negative patients, and adds Kaposi's sarcoma to the differential diagnosis of thrombocytopenia in immunosuppressed patients.
本文描述了一名慢性淋巴细胞白血病患者,在接受单磷酸氟达拉滨(FAMP)免疫抑制治疗后,出现了快速进展的卡波西肉瘤。该肿瘤的发生伴随着进行性血小板减少,这是由于血小板被困在卡波西肉瘤中,而无消耗性凝血病或微血管病性溶血性贫血的迹象。这种扣押过程可能是由肿瘤血管的异常结构引起的,导致内皮下结构如胶原蛋白、血管性血友病因子和腱生蛋白暴露于血管腔内。可见由于FAMP对多个T细胞亚群的淋巴细胞毒性作用导致严重免疫抑制。该病例证实了免疫抑制作为卡波西肉瘤发生的辅助因素在HIV阴性患者中的重要性,并将卡波西肉瘤纳入免疫抑制患者血小板减少的鉴别诊断中。