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血液系统疾病中的9号染色体三体:可能与原发性血小板增多症相关。

Trisomy 9 in hematologic disorders: possible association with primary thrombocytosis.

作者信息

Cournoyer D, Noël P, Schmidt M A, Dewald G W

出版信息

Cancer Genet Cytogenet. 1987 Jul;27(1):73-8. doi: 10.1016/0165-4608(87)90262-7.

Abstract

Ten patients with a hematologic disorder and a clone of cells with trisomy 9 in the bone marrow were studied in order to investigate the clinical significance of this chromosome anomaly. In five of the patients, trisomy 9 was the only anomaly; in four, there was also trisomy 8; and in one, a Y chromosome was also lacking. Four patients had a myelodysplastic syndrome, and six had a myeloproliferative disorder. Interestingly, four patients had primary thrombocytosis.

摘要

为了研究这种染色体异常的临床意义,对10例患有血液系统疾病且骨髓中有9号染色体三体细胞克隆的患者进行了研究。在5例患者中,9号染色体三体是唯一的异常;在4例患者中,还存在8号染色体三体;在1例患者中,还缺少一条Y染色体。4例患者患有骨髓增生异常综合征,6例患者患有骨髓增殖性疾病。有趣的是,4例患者有原发性血小板增多症。

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