Suppr超能文献

63例继发性非淋巴性血液疾病的染色体分析:一项合作研究。法国血液细胞遗传学小组。

Chromosome analysis of 63 cases of secondary nonlymphoid blood disorders: a cooperative study. Groupe Francais de Cytogénétique Hématologique.

出版信息

Cancer Genet Cytogenet. 1984 Jun;12(2):95-104. doi: 10.1016/0165-4608(84)90120-1.

Abstract

A cooperative study of secondary nonlymphoid blood disorders [dysmyelopoietic syndrome and acute nonlymphoblastic leukemia (ANLL)] was carried out on 63 patients, 8 after professional exposure to carcinogenic agents and 55 following exposure to therapeutical hazards. Clonal chromosome abnormalities were observed in 56 cases (88.9%). The most common abnormalities were hypodiploidy and structural defects. The chromosomes most often involved were #7, #5, and #17. Monosomy 7 was seen more often following malignant lymphoma than after cancer, whereas monosomy 17 seemed more common in patients formerly exposed to professional hazards. Cytogenetic "variation" is often accompanied by cytologic "variation," which could explain the high proportion of ANLL cases that are difficult to classify into the FAB system. A correlation was found between complete monosomy 7 and the presence of micromegakaryocytes and/or macroplatelets .

摘要

对63例继发性非淋巴性血液疾病[骨髓增生异常综合征和急性非淋巴细胞白血病(ANLL)]患者进行了一项合作研究,其中8例有职业性致癌物接触史,55例有治疗相关危险因素接触史。56例(88.9%)观察到克隆性染色体异常。最常见的异常是亚二倍体和结构缺陷。最常受累的染色体是7号、5号和17号。与癌症患者相比,恶性淋巴瘤患者中7号染色体单体更为常见,而17号染色体单体在既往有职业危险因素接触史的患者中似乎更为常见。细胞遗传学“变异”常伴有细胞学“变异”,这可以解释难以归入FAB系统的ANLL病例比例较高的原因。发现7号染色体完全单体与微小巨核细胞和/或大血小板的存在之间存在相关性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验