妊娠合并急性早幼粒细胞白血病1例报告及文献复习

Ying Li, Pingyong Li, Juan He, Qiong-Zhen Li
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引用次数: 0

摘要

急性早幼粒细胞白血病(APL)是急性髓系白血病(AML)的一个特殊亚群。约95%的患者有特异性染色体易位t(15≤17)(q22,q12)。APL进展迅速,其特征是广泛而严重的出血和弥漫性血管内凝血(DIC)。患者可能表现出严重的临床表现,这通常是由疾病早期DIC的发生引起的。妊娠合并APL在临床上是罕见的。它们并发症多,死亡率高,临床上难以控制。本病例报告描述了一例原发性妊娠合并APL的病例,以更好地了解如何处理此类复杂病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pregnancy Complicated with Acute Promyelocytic Leukemia: A Case Report and a Literature Review
Acute promyelocytic leukemia (APL) is a special subgroup of acute myeloid leukemia (AML). About 95% of the patients have specific chromosome translocation t (15 ≤ 17) (q22, q12). APL progresses rapidly and is characterized by extensive and severe bleeding and disseminated intravascular coagulation (DIC). Patients may present with severe clinical manifestation which is often caused by the occurrence of DIC in the early stages of the disease. Pregnancy complicated with APL is rare in the clinical setting. They have many complications, high mortality and are difficult to manage clinically. This case report describes a case of a primary pregnancy complicated with APL, in order to better understand how to manage such complex cases.
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