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美法仑治疗的多发性骨髓瘤中出现继发性髓系/自然杀伤细胞急性白血病

[Secondary myeloid/natural killer cell acute leukemia appeared in multiple myeloma treated with melphalan].

作者信息

Kaya H, Nakamura S, Yamazaki H, Kumabashiri I, Ohtake S, Matsuda T

机构信息

Third Department of Internal Medicine, Kanazawa University School of Medicine.

出版信息

Rinsho Ketsueki. 1995 Jul;36(7):682-6.

PMID:7563597
Abstract

A 67-year-old woman was treated with MP-P therapy and combination chemotherapy for multiple myeloma IgG-lambda type. After the therapy for about three years, pancytopenia developed. Bone marrow aspiration study revealed a few of myeloma cell and many atypical cells showing promyelocytic feature. Chromosomal abnormality was 46, X, -X, +8, -13, +mar. CD33 and CD56 were positive, but CD16 and HLA-DR were negative. We diagnosed as multiple myeloma complicated with secondary myeloid/natural killer (NK) cell acute leukemia. After she had been treated with low dose etoposide for leukemia, she obtained complete remission. But since myeloma progressed and the amount of M protein was increased, she was treated with dexamethasone and low dose etoposide, resulting in a decrease in the amount of M protein. After that, because of leukemic cell re-proliferation, she was treated with etoposide. However, she died of sepsis due to severe myelosuppression. This case was interesting one in coexist of multiple myeloma and secondary myeloid/NK cell acute leukemia, and those affecting her clinical course each other.

摘要

一名67岁女性因IgG-λ型多发性骨髓瘤接受MP-P疗法及联合化疗。治疗约三年后,出现全血细胞减少。骨髓穿刺检查发现少量骨髓瘤细胞及许多呈现早幼粒细胞特征的非典型细胞。染色体异常为46,X,-X,+8,-13,+mar。CD33和CD56呈阳性,但CD16和HLA-DR呈阴性。我们诊断为多发性骨髓瘤合并继发性髓系/自然杀伤(NK)细胞急性白血病。在她接受低剂量依托泊苷治疗白血病后,获得完全缓解。但由于骨髓瘤进展且M蛋白量增加,她接受了地塞米松和低剂量依托泊苷治疗,导致M蛋白量减少。此后,由于白血病细胞再次增殖,她接受了依托泊苷治疗。然而,她因严重骨髓抑制导致的败血症死亡。该病例有趣之处在于多发性骨髓瘤与继发性髓系/NK细胞急性白血病并存,且二者相互影响其临床病程。

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