Kohno M, Miyata M, Ohmoto A, Matsuyama R
Rinsho Ketsueki. 1989 Aug;30(8):1310-3.
A case of Kaposi's sarcoma developing during corticosteroid therapy for idiopathic thrombocytopenic purpura is reported. The patient is a 58-year-old female who was admitted to Sapporo City General Hospital for bleeding tendency in March 1987. She had been treated before admission with prednisolone (over 40 mg/day) for idiopathic thrombocytopenic purpura since October 1986, but her platelet count was below 40,000/microliters. In April 1987, several dark red or blue nodules appeared on the tip of her nose, left forearm, right shoulder, trunk and tongue. These nodules rapidly grew. Biopsy specimens from the nodule of the left forearm showed the histologic changes of Kaposi's sarcoma. She was treated with irradiation. Splenectomy was done in May 1987 and prednisolone was decreased to 5 mg/day. Her platelet count was continually kept 50,000/microliters or more. Her Kaposi's sarcoma completely regressed in January 1988. The relationship of immunosuppressive therapy to Kaposi's sarcoma is discussed.
报告了1例在特发性血小板减少性紫癜的皮质类固醇治疗过程中发生的卡波西肉瘤病例。患者为一名58岁女性,1987年3月因出血倾向入住札幌市立综合医院。自1986年10月以来,她因特发性血小板减少性紫癜接受泼尼松龙治疗(每日超过40毫克),但入院前血小板计数低于40,000/微升。1987年4月,她的鼻尖、左前臂、右肩、躯干和舌头出现了几个暗红色或蓝色结节。这些结节迅速增大。左前臂结节的活检标本显示了卡波西肉瘤的组织学变化。她接受了放射治疗。1987年5月进行了脾切除术,泼尼松龙减至每日5毫克。她的血小板计数持续保持在50,000/微升或以上。她的卡波西肉瘤于1988年1月完全消退。文中讨论了免疫抑制治疗与卡波西肉瘤的关系。