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[一例伴有核型异常的慢性中性粒细胞白血病]

[A case of chronic neutrophilic leukemia with abnormal karyotype].

作者信息

Kunishima S, Mizuno R, Fujishiro N, Ohno R

出版信息

Rinsho Byori. 1989 Aug;37(8):943-7.

PMID:2585758
Abstract

A 75-year-old man was admitted to our hospital because of leukocytosis and thrombocytosis. The peripheral blood showed RBC 403 x 10(4)/microliters, Hb 14.1 g/dl, PLT 91 x 10(4)/microliters, and WBC 48,000/microliters with a differential count of 24% band forms, 65% segmented forms and 11% others. The bone marrow aspiration revealed myeloid hyperplasia (94.4% myeloid series, 4.8% erythroid series and 0.8% others), and NAP score was consistently high. The serum level of lysozyme and vitamin B12 were elevated. There were no signs of infection or other malignancy. Cytogenetic study of bone marrow cells showed mosaic karyotypes of 46,XY/46,XY,t(7;16) (q22;q24). The Ph1 chromosome was not found. A diagnosis of chronic neutrophilic leukemia was made. Serial chromosomal analysis showed the coexistence of a clone with 46,XY,t(7;16) (q22;q24) and that with 46, XY.

摘要

一名75岁男性因白细胞增多和血小板增多入住我院。外周血检查显示红细胞403×10⁴/微升,血红蛋白14.1克/分升,血小板91×10⁴/微升,白细胞48,000/微升,分类计数显示杆状核细胞占24%,分叶核细胞占65%,其他占11%。骨髓穿刺显示骨髓增生(髓系94.4%,红系4.8%,其他0.8%),中性粒细胞碱性磷酸酶(NAP)积分持续升高。血清溶菌酶和维生素B₁₂水平升高。无感染或其他恶性肿瘤迹象。骨髓细胞的细胞遗传学研究显示为46,XY/46,XY,t(7;16)(q22;q24)的嵌合核型。未发现Ph1染色体。诊断为慢性中性粒细胞白血病。系列染色体分析显示存在46,XY,t(7;16)(q22;q24)的克隆与46,XY的克隆共存。

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