[染色体易位 t(16;17)的 APL 样白血病：病例报告和文献综述]。

Q3 Medicine

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi Pub Date : 2024-09-14 DOI:10.3760/cma.j.cn121090-20240118-00033

Q Wang, T X Lyu, H Ai, X D Lyu, Q S Yin

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引用次数: 0

摘要

变异型急性早幼粒细胞白血病（APL）和APL样白血病是APL的罕见类型，其中t（16;17）染色体异常更为罕见。我院收治了一名 t（16;17）染色体异常的 APL 样患者，其特点是骨骼、淋巴结和中枢神经系统受累。经过几个周期的化疗后，他的病情完全缓解，随后接受了造血干细胞移植。此外，还报告了该患者的诊断和治疗情况，并进行了文献综述。

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查看原文本刊更多论文

[APL-like leukemia with chromosomal translocation t(16;17): a case report and literature review].

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.

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来源期刊

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi Medicine-Medicine (all)

CiteScore

0.80

自引率

0.00%

发文量

100