四体
医学
三体8
髓样肉瘤
荧光原位杂交
髓系白血病
三体
病理
骨髓
CD33
髓样
化疗
白血病
内科学
核型
生物
染色体
遗传学
干细胞
川地34
基因
作者
Tohru Takahashi,Hiroyuki Tsukuda,Hirokazu Kimura,Mitsuru Yoshimoto,Masayuki Tsujisaki
出处
期刊:Internal Medicine
[Japanese Society of Internal Medicine]
日期:2010-01-01
卷期号:49 (5): 447-451
被引量:8
标识
DOI:10.2169/internalmedicine.49.2904
摘要
This report describes a patient with extramedullary relapse of acute myeloid leukemia (AML) without involving bone marrow. A 57-year-old man was diagnosed as having acute monoblastic leukemia with t(9;11)(p22;q23) and trisomy 8. Ten months after achieving complete response (CR) with chemotherapy, masses developed in his left forearm and in the back of his thigh, preceded by enigmatic peripheral neurological symptoms. Aspiration from the forearm showed leukemic relapse, and fluorescence in situ hybridization (FISH) revealed that the majority of the cells had 11q23 anomaly and tetrasomy 8. Bone marrow or meningeal relapse was not observed. To our knowledge, this is the first case report of clonal evolution associated with the development of myeloid sarcoma as a relapse in AML.
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