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两种并存的骨髓增殖性疾病中的染色体异常

Chromosomal anomalies in two coexistent myeloproliferative disorders.

作者信息

Ganti Apar Kishor, Potti Anil, Mehdi Syed A

机构信息

Department of Internal Medicine, University of North Dakota School of Medicine and Health Sciences, Fargo, ND 58102, USA.

出版信息

Cancer Genet Cytogenet. 2003 Sep;145(2):172-5. doi: 10.1016/s0165-4608(03)00095-5.

Abstract

A 58-year-old male presented with fatigue, tiredness, and pruritus after hot showers and an elevated white blood cell count (20000/mm(3)). A diagnosis of polycythemia vera (PV) was made after investigation revealed a low erythropoietin and elevated leukocyte alkaline phosphatase (LAP) score; he was treated with repeated phlebotomies. Two years later he developed elevated white counts again and investigation revealed Philadelphia chromosome positive (19/20 cells) chronic myelocytic leukemia (CML). The karyotype also revealed trisomy 9 in 1 of 20 cells. He was treated with imatinib mesylate and went into clinical, hematologic, cytogenetic, and molecular remission. Repeat chromosomal analysis revealed absence of Philadelphia chromosome and BCR/ABL translocation but presence of trisomy 9. To our knowledge, this is the first reported case of coexisting PV and CML both associated with separate chromosomal abnormalities. This also raises an interesting therapeutic consideration of using concomitant imatinib mesylate and hydroxyurea.

摘要

一名58岁男性,在热水淋浴后出现疲劳、乏力和瘙痒,白细胞计数升高(20000/mm³)。检查发现促红细胞生成素水平降低、白细胞碱性磷酸酶(LAP)评分升高后,诊断为真性红细胞增多症(PV);对其进行了反复放血治疗。两年后,他的白细胞计数再次升高,检查发现费城染色体阳性(20个细胞中有19个),诊断为慢性粒细胞白血病(CML)。核型分析还显示20个细胞中有1个存在9号染色体三体。他接受了甲磺酸伊马替尼治疗,并实现了临床、血液学、细胞遗传学和分子学缓解。重复染色体分析显示费城染色体和BCR/ABL易位均消失,但仍存在9号染色体三体。据我们所知,这是首例报道的同时存在PV和CML且两者均与不同染色体异常相关的病例。这也引发了关于联合使用甲磺酸伊马替尼和羟基脲的有趣治疗思考。

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