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[别嘌醇诱发骨髓增殖性疾病患者全血细胞减少症]

[Allopurinol induced pancytopenia in a patient with myeloproliferative disorder].

作者信息

Shinagawa A, Itoh T, Komeno T, Komatsu T, Hasegawa Y, Kobayashi T, Kozima H, Ninomiya H, Nagasawa T, Abe T

机构信息

Division of Hematology, University of Tsukuba.

出版信息

Rinsho Ketsueki. 1997 Jan;38(1):64-71.

PMID:9028164
Abstract

We reported a rare case of pancytopenia caused by allopurinol. A 61-year-old man was first admitted in May 1993, because of thrombocytosis. He had suffered from chronic glomerulonephritis. He was administered allopurinol for hyperuricemia from March 1993. On first admission the laboratory findings revealed leukocytosis (10,100/microliter) and thrombocytosis (971 x 10(3)/microliter) in the peripheral blood. Myelofibrosis was strongly suspected due to increased number of MgK and reticular fiber in the bone marrow. Two months later, he readmitted due to pancytopenia (WBC 1,300/microliter, Hb 6.2g/dl, Plt 10 x 10(3)/microliter). His bone marrow showed markedly hypocellular. Because we suspected that pancytopenia was induced by allopurinol, we discontinued allopurinol and administered oxymetholone, G-CSF, and EPO, WBC, RBC, and platelet count had been recovered about one and half months later. In vitro co-culture indicated that CFU-G, E, and Meg in the bone marrow cells after recovery from pancytopenia were markedly suppressed in the presence of patient's serum and oxipurinol. Pancytopenia due to allopurinol was reported to be rare, and some authors showed that it will sometimes be fatal. Because pancytopenia of this case had been recovered in a relatively short time with cytokine therapy, it was thought to be effective for pancytopenia due to drug like this case.

摘要

我们报告了一例由别嘌醇引起的全血细胞减少症的罕见病例。一名61岁男性于1993年5月因血小板增多症首次入院。他患有慢性肾小球肾炎。自1993年3月起,他因高尿酸血症接受别嘌醇治疗。首次入院时,实验室检查发现外周血白细胞增多(10,100/微升)和血小板增多(971×10³/微升)。由于骨髓中MgK和网状纤维数量增加,强烈怀疑为骨髓纤维化。两个月后,他因全血细胞减少症再次入院(白细胞计数1,300/微升,血红蛋白6.2克/分升,血小板计数10×10³/微升)。他的骨髓显示明显细胞减少。由于我们怀疑全血细胞减少症是由别嘌醇引起的,我们停用了别嘌醇,并给予羟甲烯龙、粒细胞集落刺激因子和促红细胞生成素,白细胞、红细胞和血小板计数在大约一个半月后恢复。体外共培养表明,全血细胞减少症恢复后的骨髓细胞中的CFU-G、E和Meg在患者血清和氧嘌呤醇存在的情况下受到明显抑制。据报道,别嘌醇引起的全血细胞减少症很罕见,一些作者表明它有时会致命。由于该病例的全血细胞减少症通过细胞因子治疗在相对较短的时间内得到了恢复,因此认为这种治疗方法对这种药物引起的全血细胞减少症有效。

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