APL-like leukemia with chromosomal translocation t(16;17): a case report and literature review
10.3760/cma.j.cn121090-20240118-00033
- VernacularTitle:伴有t(16;17)染色体异常的APL样白血病1例报告并文献复习
- Author:
Qian WANG
1
;
Tianxin LYU
;
Hao AI
;
Xiaodong LYU
;
Qingsong YIN
Author Information
1. 郑州大学附属肿瘤医院（河南省肿瘤医院），郑州 450008
- From:
Chinese Journal of Hematology
2024;45(9):856-860
- CountryChina
- Language:Chinese
-
Abstract:
Variant acute promyelocytic leukemia (APL) and APL-like leukemia are rare types of APL, with t (16;17) chromosome abnormality being even rarer. An APL-like patient with t (16;17) chromosome abnormality, which was characterized by bone, lymph node, and central nervous system involvement, was admitted to our hospital. He achieved complete remission after several cycles of chemotherapy and subsequently underwent hematopoietic stem cell transplantation. Furthermore, the diagnosis and treatment of this patient were reported and a literature review was conducted.
