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[小剂量柔红霉素联合口服泼尼松龙治疗慢性粒细胞白血病急变期逆转至慢性期]

[Reversion to chronic phase of chronic myelogenous leukemia in blast crisis with small-dose daunorubicin and oral prednisolone].

作者信息

Kuyama J, Take H

机构信息

Department of Internal Medicine, Toyoanaka Municipal Hospital.

出版信息

Rinsho Ketsueki. 1995 Dec;36(12):1353-8.

PMID:8587171
Abstract

In December 1993, a 76-year-old Japanese male presented with general fatigue. Peripheral blood (PB) examination indicated marked leukocytosis (WBC count, 19.8 x 10(4)/microliter; leukemic blast differential, 89.5%). Leukemic blasts were positive for CD33, and negative for lymphoid antigens, with 2% of the blasts being positive for myeloperoxidase staining. On admission, chromosome analysis of leukemic cells in PB showed 45, X,-Y, t (9;22) [12/15]/46, XY, t (9;22) [3/15]. Southern blot analysis of the DNA from PB showed a rearrangement at the M-BCR region and germline configurations of both TCR beta and IgH chain genes. The patient was diagnosed as Philadelphia-positive chronic myelogenous leukemia (CML) in blast crisis. We commenced treatment with daunorubicin (DNR; 20 mg/day x 1 IV) and daily prednisolone (PSL; 60 mg/day PO). Leukemic blasts disappeared rapidly from PB, while the promyelocytes showed a transient increase, peaked 7 days after the start of therapy, and then disappeared. Myelocytes and metamyelocytes also showed transient increases. Without a period of severe myelosuppression, the patient reverted to the chronic phase of CML and karyotypic analysis of bone marrow cells showed 45, X,-Y, t (9;22) [33/35]/46, XY, [2/35]. Consolidation chemotherapy with DNR and BHAC was started, but the patient's condition deteriorated due to bacterial infection and he died of hepatic failure on March 1994. In this case, reversion to the chronic phase of CML in blast crisis may be accomplished by the cytodifferentiating effects of small-dose DNR and oral PSL to the leukemic blasts.

摘要

1993年12月,一名76岁的日本男性因全身乏力就诊。外周血(PB)检查显示白细胞显著增多(白细胞计数为19.8×10⁴/微升;白血病原始细胞比例为89.5%)。白血病原始细胞CD33呈阳性,淋巴样抗原呈阴性,2%的原始细胞髓过氧化物酶染色呈阳性。入院时,外周血白血病细胞的染色体分析显示为45,X,-Y,t(9;22)[12/15]/46,XY,t(9;22)[3/15]。外周血DNA的Southern印迹分析显示M-BCR区域发生重排,TCRβ和IgH链基因均为种系构型。该患者被诊断为费城染色体阳性的慢性粒细胞白血病(CML)急变期。我们开始用柔红霉素(DNR;20毫克/天×1次静脉注射)和每日泼尼松龙(PSL;60毫克/天口服)进行治疗。白血病原始细胞迅速从外周血中消失,而早幼粒细胞出现短暂增加,在治疗开始后7天达到峰值,然后消失。中幼粒细胞和晚幼粒细胞也出现短暂增加。在没有严重骨髓抑制期的情况下,患者恢复到CML慢性期,骨髓细胞的核型分析显示为45,X,-Y,t(9;22)[33/35]/46,XY,[2/35]。开始用DNR和BHAC进行巩固化疗,但患者因细菌感染病情恶化,于1994年3月死于肝功能衰竭。在这种情况下,CML急变期恢复到慢性期可能是通过小剂量DNR和口服PSL对白血病原始细胞的诱导分化作用实现的。

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