Inoue T, Furukawa Y, Yamane T, Sasaki A, Im T, Tatsumi N, Sannomiya Y
Rinsho Ketsueki. 1989 Apr;30(4):541-5.
A 55-year-old woman developed a secondary leukemia following 1-year treatment of Hodgkin's disease. She was admitted to our hospital because of the celiac lymphadenopathy. Open laparotomy was performed. Biopsy specimens of the lymph node demonstrated Reed Sternberg cells with mature lymphocytes. She was diagnosed as having Hodgkin's disease (lymphocyte predominant type). She was treated by the combination chemotherapy consisting of mitoxantrone, cyclophosphamide, vincristine and prednisolone for Hodgkin's disease in November 1986. Hodgkin's disease achieved complete remission and she was regularly followed. No abnormal findings were observed in the peripheral blood and bone marrow. But thrombocytopenia and the blastoid cells appeared in the peripheral blood in February 1988. The bone marrow specimen was hypercellular and occupied by 90% of blastoid cells that were positive for peroxidase staining. She was diagnosed as having AML from the bone marrow aspiration and biopsy specimens. She did not respond to several chemotherapy regimens and now she is treated by low dose Ara C.
一名55岁女性在接受霍奇金病治疗1年后发生了继发性白血病。她因腹腔淋巴结病入住我院。行剖腹探查术。淋巴结活检标本显示有里德·斯腾伯格细胞和成熟淋巴细胞。她被诊断为霍奇金病(淋巴细胞为主型)。1986年11月,她接受了由米托蒽醌、环磷酰胺、长春新碱和泼尼松龙组成的联合化疗方案治疗霍奇金病。霍奇金病达到完全缓解,此后她接受定期随访。外周血和骨髓未观察到异常发现。但1988年2月外周血出现血小板减少和原始细胞。骨髓标本细胞增多,90%为原始细胞,过氧化物酶染色阳性。通过骨髓穿刺和活检标本,她被诊断为急性髓系白血病。她对多种化疗方案均无反应,目前正在接受小剂量阿糖胞苷治疗。