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t(15;17) 超颗粒型急性早幼粒细胞白血病(M3)在复发时发展为无t(15;17)的t(3;6) M3。

t(15;17) hypergranular acute promyelocytic leukemia (M3) developing into a t(3;6) M3 without t(15;17) at relapse.

作者信息

Desangles F, Vilain E, Arborio M, De Revel T, Flandrin G

机构信息

Laboratoire de Biologie Clinique, HIA Val de Grâce, Paris, France.

出版信息

Leuk Lymphoma. 1995 Sep;19(1-2):185-8. doi: 10.3109/10428199509059675.

DOI:10.3109/10428199509059675
PMID:8574167
Abstract

This report describes a case of acute promyelocytic leukemia (APL) M3. At diagnosis, the specific t(15;17) translocation was observed. After chemotherapy including retinoic acid, a complete remission was achieved and the karyotype became normal. At relapse of the M3 leukemia, the t(15;17) clone was no longer observed but a t(3;6) translocation was then detected. Several hypotheses for this unusual cytogenetic course of APL are discussed.

摘要

本报告描述了一例急性早幼粒细胞白血病(APL)M3型病例。诊断时,观察到特异性t(15;17)易位。在包括维甲酸在内的化疗后,实现了完全缓解,核型恢复正常。在M3白血病复发时,未再观察到t(15;17)克隆,但随后检测到t(3;6)易位。本文讨论了APL这种不寻常细胞遗传学过程的几种假说。

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