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骨髓增生异常综合征患者的细胞遗传学分析。

Cytogenetic analysis in patients with myelodysplastic syndrome.

作者信息

Hu N, Bian M

机构信息

Cancer Institute, CAMS, Beijing.

出版信息

Proc Chin Acad Med Sci Peking Union Med Coll. 1990;5(3):135-9.

PMID:2098765
Abstract

Forty-six patients with myelodysplastic syndrome (MDS) were studied. Chromosomal abnormalities were observed in 20 of the 46 patients (43%). Abnormalities of chromosome No. 5 occurred in 6 patients (13%); four of them had a deletion of the long arm of this chromosome [del (5q)]. Four patients had monosomy 7 (8.6%), and six patients had trisomy 8 (13%). Our results suggest that chromosomal abnormalities, deletion (5q), monosomy 7 and trisomy 8, might play important roles in the pathogenesis of MDS.

摘要

对46例骨髓增生异常综合征(MDS)患者进行了研究。46例患者中有20例(43%)观察到染色体异常。6例患者(13%)出现5号染色体异常;其中4例该染色体长臂缺失[del(5q)]。4例患者有7号染色体单体(8.6%),6例患者有8号染色体三体(13%)。我们的结果表明,染色体异常、5号染色体长臂缺失、7号染色体单体和8号染色体三体可能在MDS的发病机制中起重要作用。

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