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[小剂量N4-山嵛酰-1-β-D-阿拉伯呋喃糖基胞嘧啶成功治疗1例慢性粒-单核细胞白血病急变期]

[Successful treatment with a small dose of N4-behenoyl-1-beta-D-arabinofuranosylcytosine in a case of chronic myelomonocytic leukemia in blastic crisis].

作者信息

Tsukada J, Misago M, Sato T, Kikuchi M, Nakata K, Nagata K, Mori N, Otani H, Oda S, Chiba S

出版信息

Rinsho Ketsueki. 1989 Jan;30(1):61-6.

PMID:2716200
Abstract

A 56-year-old female was admitted for the examination of leukocytosis in May, 1982. The hematological examination showed hemoglobin 12.0g/dl, platelets 14.5 X 10(4)/microliters and leukocytes 18,000/microliters with 28% of monocytes. A bone marrow aspiration revealed granulocytic hyperplasia. Granulocytes showed nuclear abnormalities, such as folding or lobulation. From these data, a diagnosis of chronic myelomonocytic leukemia (CMMoL) was made and followed with no treatment for 2 years. However, fever, bone pain, anemia, thrombocytopenia and the increase of monoblasts in the peripheral blood and bone marrow were observed in May, 1984. These findings indicated that she was in the blastic phase. She was treated by intensive combination chemotherapy (BHAC-AMP), but did not attain any remission. Therefore, a small dose of N4-behenoyl-1-beta-D-arabinofuranosylcytosine (BH-AC; 1 mg/kg/day) was administered for 70 days. As a result, complete remission was obtained and continued for 37 months with the same therapy. The experience of this case suggests that small dose of BH-AC could be applied to a case of CMMoL in blastic crisis.

摘要

一名56岁女性于1982年5月因白细胞增多入院检查。血液学检查显示血红蛋白12.0g/dl,血小板14.5×10⁴/微升,白细胞18,000/微升,单核细胞占28%。骨髓穿刺显示粒细胞增生。粒细胞显示核异常,如折叠或分叶。根据这些数据,诊断为慢性粒单核细胞白血病(CMMoL),并随访2年未治疗。然而,1984年5月观察到发热、骨痛、贫血、血小板减少以及外周血和骨髓中原始单核细胞增加。这些发现表明她处于原始细胞期。她接受了强化联合化疗(BHAC-AMP),但未达到任何缓解。因此,给予小剂量的N⁴-二十二酰基-1-β-D-阿拉伯呋喃糖基胞嘧啶(BH-AC;1mg/kg/天),持续70天。结果获得完全缓解,并采用相同疗法持续37个月。该病例的经验表明,小剂量的BH-AC可应用于处于原始细胞危象的CMMoL病例。

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