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[急性髓系白血病伴inv(16)(p13q22)的巨大淋巴结病:一例报告]

[Bulky lymphadenopathy in acute myeloid leukemia with inv (16) (p13q22): a case report].

作者信息

Zhou Hui-Fen, Li Jian-Yong, Qian Si-Xuan, Qiu Hai-Rong, Zhang Su-Jiang, Zhang Jian-Fu, Wu Yu-Jie, Shen Rui-Lan

机构信息

Department of Hematology, The First Affiliated Hospital, Nanjing Medical University, Jiangsu Province Hospital, Nanjing 210029, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2006 Oct;14(5):1033-7.

Abstract

The study was aimed to investigate the different prognosis of acute myeloid leukemia (AML) with inv (16). A 13-year-old patient diagnosed as M4Eo presenting with bulky lymphadenopathy was reported, the curative process of patients was presented and the related issues were discussed. The karyotype and inv (16) were detected by conventional cytogeneties and fluorescence in situ hybridization (FISH), respectively, the immunophenotype was detected by flow cytometry. The results showed that conventional cytogenetics and FISH analysis revealed inv (16). Induction therapy included idarubicin and cytarabine. After complete remission, patient received consolidation theray containing high-dose cytarabine (HDAC). FISH analysis revealed poor response of patient to HDAC. It is concluded that bulky lymphadenopathy in AML with inv (16) may be a negative prognostic sign. FISH for inv (16) is specific and constitutes an reliable tool to be used for diagnosis and minimal residual disease (MRD).

摘要

本研究旨在探讨伴有inv(16)的急性髓系白血病(AML)的不同预后。报告了1例诊断为M4Eo且伴有巨大淋巴结病的13岁患者,介绍了患者的治疗过程并讨论了相关问题。分别采用传统细胞遗传学和荧光原位杂交(FISH)检测核型和inv(16),采用流式细胞术检测免疫表型。结果显示,传统细胞遗传学和FISH分析均发现inv(16)。诱导治疗包括伊达比星和阿糖胞苷。完全缓解后,患者接受了含大剂量阿糖胞苷(HDAC)的巩固治疗。FISH分析显示患者对HDAC反应不佳。结论是,伴有inv(16)的AML中的巨大淋巴结病可能是一个不良预后标志。用于检测inv(16)的FISH具有特异性,是用于诊断和微小残留病(MRD)的可靠工具。

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