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一名患有骨髓增生异常综合征伴骨髓纤维化患者的18号染色体长臂等臂染色体。

An isochromosome of the long arm of chromosome 18 in a patient with myelodysplastic syndrome with myelofibrosis.

作者信息

Xue Y, Cao Y, Gao Y, Xie X, Lu D, Chen Z

机构信息

Jiangsu Institute of Hematology, Leukemia Research Unit, Suzhou Medical College, PR China.

出版信息

Cancer Genet Cytogenet. 1995 Feb;79(2):149-52. doi: 10.1016/0165-4608(94)00136-y.

Abstract

A case of myelodysplastic syndrome (MDS) with myelofibrosis and i(18q) is reported. The patient, a 29-year-old Chinese man, was noted to be anemic over a 10-year period. Recently, his spleen became progressively massive and bone marrow aspirates yielded "dry taps" on several occasions. Hematologic investigation disclosed pancytopenia, numerous nucleated red cells, and slightly increased myeloblasts (8%) in the peripheral blood. Bone marrow aspirate and biopsy revealed hypercellular marrow, trilineage dysplasia, and significant reticulin fibrosis, but without collagen formation. Bone marrow karyotypic analysis with R-banding showed an isochromosome 18q as a sole abnormality in 20 of 24 metaphases analysed. The patient died of severe anemia and bleeding due to bone marrow failure. We believe that i(18q) and myelofibrosis may be related to his poor prognosis.

摘要

报告了1例伴有骨髓纤维化和i(18q)的骨髓增生异常综合征(MDS)。患者为一名29岁的中国男性,在10年期间被发现患有贫血。最近,他的脾脏逐渐肿大,多次骨髓穿刺均出现“干抽”。血液学检查发现全血细胞减少、外周血中有大量有核红细胞以及原始粒细胞略有增加(8%)。骨髓穿刺和活检显示骨髓细胞增多、三系发育异常以及明显的网状纤维纤维化,但无胶原形成。采用R显带技术的骨髓核型分析显示,在分析的24个中期细胞中有20个存在等臂染色体18q,为唯一异常。患者死于严重贫血和骨髓衰竭导致的出血。我们认为i(18q)和骨髓纤维化可能与他的不良预后有关。

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