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与克兰费尔特综合征相关的原发性骨髓化生:一例报告

Agnogenic myeloid metaplasia associated with Klinefelter syndrome: a case report.

作者信息

Kumar S, Menke D M, Dewald G W, Colon-Otero G

机构信息

Division of Hematology and Internal Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Ann Hematol. 2002 Apr;81(4):215-8. doi: 10.1007/s00277-002-0430-2. Epub 2002 Mar 7.

Abstract

Klinefelter syndrome is the most commonly diagnosed sex chromosome disorder among males. It is usually associated with 47 chromosomes, including two Xs and one Y. The formal cytogenetic designation for Klinefelter syndrome is 47, XXY; the extra sex chromosome is due to meiotic chromosomal nondisjunction. Increased risk of various malignant diseases has been recognized among patients with different congenital chromosomal abnormalities. Since the early 1960s, numerous reports have appeared of an increased risk of malignant neoplasms among patients with Klinefelter syndrome. Evidence suggests a correlation with increased incidences of germ cell tumors and breast cancers. Whether these patients are at an increased risk of hematologic malignant disease, especially acute leukemia, is still uncertain. This report describes a patient with agnogenic myeloid metaplasia and Klinefelter syndrome, an association not previously reported.

摘要

克兰费尔特综合征是男性中最常被诊断出的性染色体疾病。它通常与47条染色体相关,包括两条X染色体和一条Y染色体。克兰费尔特综合征的正式细胞遗传学命名为47, XXY;额外的性染色体是由于减数分裂时染色体不分离所致。在患有不同先天性染色体异常的患者中,已认识到患各种恶性疾病的风险增加。自20世纪60年代初以来,已有大量报告指出克兰费尔特综合征患者患恶性肿瘤的风险增加。有证据表明与生殖细胞肿瘤和乳腺癌的发病率增加有关。这些患者患血液系统恶性疾病尤其是急性白血病的风险是否增加仍不确定。本报告描述了一名患有特发性骨髓化生和克兰费尔特综合征的患者,这种关联此前未见报道。

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