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[伴有维生素B12缺乏的非典型白血病]

[Atypical leukemia accompanied by vitamin B12 deficiency].

作者信息

Tsukamoto N, Inose K, Matsushima T, Uchiyama T, Sugita Y, Takeuchi T, Sato S, Omine M, Naruse T

机构信息

Division of Internal Medicine, Takasaki National Hospital.

出版信息

Rinsho Ketsueki. 1992 Apr;33(4):461-6.

PMID:1602609
Abstract

A 76 year old female with atypical leukemia complicated by vitamin B12 deficiency demonstrated marked fluctuation in blast percentage and hemopoiesis over 8 month period. She underwent surgical removal of pancreas head cancer 5.5 years ago. In January 1989 severe pancytopenia and mild increase of bone marrow blast were found. Blood transfusions and inadvertent administration of Vitamin B12 resulted in alleviation of pancytopenia and decrease in blast percentage. Several months later her bone marrow blast exceeded 30%, when serum B12 concentration was below 90 pg/ml. B12 injection and blood transfusion resulted in significant improvement in her hematological condition, but shortly thereafter she died of fulminant hepatitis. Her bone marrow cells showed a polyclonal constitution, as assessed by the RFLP-methylation technique using the PGK gene as a probe. The coexistence of leukemic- and normal clones under Vitamin B12 deficiency conditions and the differing behavior of such clones to B12 supplementation may explain the unusual clinical course observed in this patient.

摘要

一名76岁女性,患有非典型白血病并伴有维生素B12缺乏,在8个月的时间里原始细胞百分比和造血功能出现明显波动。她于5.5年前接受了胰头癌手术切除。1989年1月,发现严重全血细胞减少和骨髓原始细胞轻度增加。输血和无意中给予维生素B12导致全血细胞减少缓解和原始细胞百分比下降。几个月后,当血清B12浓度低于90 pg/ml时,她的骨髓原始细胞超过30%。注射B12和输血使她的血液学状况有显著改善,但此后不久她死于暴发性肝炎。通过使用PGK基因作为探针的RFLP-甲基化技术评估,她的骨髓细胞显示出多克隆构成。维生素B12缺乏条件下白血病克隆和正常克隆的共存以及这些克隆对补充B12的不同反应可能解释了该患者观察到的不寻常临床病程。

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