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治疗相关的急性早幼粒细胞白血病:一例病例报告及文献综述

Therapy-Related Acute Promyelocytic Leukemia: A Case Report and a Review of Literature.

作者信息

Foster Dawson, Nair Hari K, Robbins Katherine, Rajeh Nabeel

机构信息

Internal Medicine, St. Luke's Hospital, Chesterfield, USA.

Hematology Oncology, Saint Louis University School of Medicine, St. Louis, USA.

出版信息

Cureus. 2023 Jul 17;15(7):e42008. doi: 10.7759/cureus.42008. eCollection 2023 Jul.

Abstract

Acute promyelocytic leukemia (APL) is a subgroup of acute myeloid leukemia (AML), and while not a common form of cancer, it does make up a modest portion of acute leukemia. The genetic hallmark of APL is the t(15;17)(q24.1;q21.2) promyelocytic leukemia/retinoic acid receptor alpha (PML/RARA) protein. We present the case of a patient who had undergone prior therapy for stage IIIC squamous cell carcinoma of the anorectal region with 5-fluorouracil, mitomycin C, and radiation and developed therapy-related acute promyelocytic leukemia about 18 months later. We also review the clinical features and management of APL while also highlighting that therapy-related APL, although uncommon, can develop from chemoradiation. The specific diagnosis of therapy-related APL is its own distinct diagnosis, but its treatment remains the same as primary APL.

摘要

急性早幼粒细胞白血病(APL)是急性髓系白血病(AML)的一个亚组,虽然它不是一种常见的癌症形式,但它在急性白血病中确实占了相当一部分。APL的基因特征是t(15;17)(q24.1;q21.2)早幼粒细胞白血病/维甲酸受体α(PML/RARA)蛋白。我们报告了一例患者,该患者曾接受过5-氟尿嘧啶、丝裂霉素C和放疗治疗IIIC期肛管区域鳞状细胞癌,约18个月后发生了治疗相关的急性早幼粒细胞白血病。我们还回顾了APL的临床特征和管理,同时强调治疗相关的APL虽然不常见,但可由放化疗引起。治疗相关APL的具体诊断是其独特的诊断,但治疗方法与原发性APL相同。

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