Schmitt T, Mathiot C, Benveniste M, Varet B, Levy J P
Nouv Presse Med. 1979 May 26;8(23):1923-5.
The association of Kaposi angiosarcomatosis and an auto-immune haemolytic anaemia is reported in a 69-year-old woman. The direct Coombs test was "igG complement" type positive. This is the 5th reported case and the 2nd in which haemolysis developed during an acute malignant exacerbation of the disease. The patient died less than 4 months following the diagnosis of Kaposi's sarcoma, after treatment with prednisone and chlorambucil. Lymphoid and immunological abnormalities are not rare during the course of Kaposi's sarcoma. The reasons are discussed briefly.
据报道，一名69岁女性患有卡波西血管肉瘤合并自身免疫性溶血性贫血。直接抗人球蛋白试验呈“IgG补体”型阳性。这是第5例报告病例，也是第2例在疾病急性恶性加重期发生溶血的病例。该患者在诊断为卡波西肉瘤后，接受泼尼松和苯丁酸氮芥治疗，不到4个月便去世。在卡波西肉瘤病程中，淋巴和免疫异常并不罕见。文中简要讨论了相关原因。
