Shiraishi J, Sudo Y, Katori Y, Akiyama M, Takada O, Maki K, Sawada K, Inaba T, Shimazaki C, Nakagawa M
Department of Internal Medicine, Ohmihachiman City Hospital.
Rinsho Ketsueki. 1998 Aug;39(8):600-5.
A 46-year-old man who had been treated with azathioprine (150 mg/day) and prednisolone (7.5-10 mg/day) for 16 years after allogeneic renal transplantation was admitted to our hospital in July 1996 for evaluation of pancytopenia. Three years earlier he had been given a diagnosis of renal pelvic and ureteral cancer, and underwent left nephrectomy with total uretectomy. His bone marrow was normocellular with excess of blasts (27.6%), and displayed trilineage myelodysplasia. A chromosomal analysis of the bone marrow revealed 43-45, XY with del (1) (p13), -5, del (7) (q22), -17, -18, and -19. The patient was given a diagnosis of refractory anemia with excess of blasts in transformation (RAEB in T), and treated with idarubicin and cytosine arabinoside. Two months later, overt acute leukemia developed and reinduction chemotherpay was started, but the patient died of cerebral hemorrhage in October. This case suggests that immunosuppressive agents such as azathioprine might play an important role in the pathogenesis of MDS (RAEB in T) and renal pelvic and ureteral cancer after renal transplantation.
一名46岁男性,在接受同种异体肾移植后,使用硫唑嘌呤(150毫克/天)和泼尼松龙(7.5 - 10毫克/天)治疗了16年。1996年7月因全血细胞减少症入院我院评估。三年前,他被诊断为肾盂输尿管癌,并接受了左肾切除术及全输尿管切除术。其骨髓细胞正常,但原始细胞增多(27.6%),显示三系骨髓发育异常。骨髓染色体分析显示为43 - 45,XY,伴有del(1)(p13)、-5、del(7)(q22)、-17、-18和-19。该患者被诊断为难治性贫血伴原始细胞增多的转化型(RAEB - T),并接受了去甲氧柔红霉素和阿糖胞苷治疗。两个月后,发生明显的急性白血病并开始再次诱导化疗,但患者于10月死于脑出血。该病例提示,硫唑嘌呤等免疫抑制剂可能在肾移植后骨髓增生异常综合征(RAEB - T)及肾盂输尿管癌的发病机制中起重要作用。