急性早幼粒细胞白血病和Brugada综合征:三氧化二砷/全反式视黄酸治疗的安全性报告。

IF 1.1 Q4 HEMATOLOGY Hematology Reports Pub Date : 2023-07-17 DOI:10.3390/hematolrep15030045
Giorgio Rosati, Sofia Camerlo, Matteo Dalmazzo, Melissa Padrini, Tiziano Tommaso Busana, Marco De Gobbi, Alessandro Fornari, Alessandro Morotti
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引用次数: 0

摘要

急性早幼粒细胞白血病(APL)是一种罕见的侵袭性急性髓性白血病(AML)。代替细胞毒性化疗,全反式维甲酸(ATRA)和三氧化二砷(ATO)的联合治疗代表了低风险患者的一线治疗。然而,如果同时诊断为Brugada综合征(BrS),则治疗方法可能具有挑战性,Brugada综合征是一种以心律失常和心源性猝死风险增加为特征的遗传性疾病。在这里,我们提出了一例BrS患者,他被诊断为低风险APL,并接受ATRA和ATO治疗,但未观察到心律失常事件。特别是,我们强调临床医生在诊断检查和选择这些患者的最佳治疗时遇到的困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Acute Promyelocytic Leukemia and Brugada Syndrome: A Report on the Safety of Arsenic Trioxide/All-Trans-Retinoic Acid Therapy.

Acute promyelocytic leukemia (APL) is a rare and aggressive form of acute myeloid leukemia (AML). Instead of cytotoxic chemotherapy, a combination of all-trans-retinoic acid (ATRA) and arsenic trioxide (ATO) represents front-line therapy in low-risk patients. However, the therapeutic approach could be challenging in the case of a concomitant diagnosis of Brugada syndrome (BrS), a genetic disease characterized by an increased risk of arrhythmias and sudden cardiac death. Here, we present the case of a BrS patient who has been diagnosed with low-risk APL and treated with ATRA and ATO without observing arrhythmic events. In particular, we highlight the difficulties encountered by clinicians during the diagnostic work-up and the choice of the best treatment for these patients.

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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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