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以非典型胸痛为表现最终诊断为急性早幼粒细胞白血病:一例报告

Atypical Chest Pain Leading to the Diagnosis of Acute Promyelocytic Leukemia: A Case Report.

作者信息

Dennis Roy L, Dorsey Dade, Scott Mitchell, Shaban Ahmed, Himes Seraphim

机构信息

Internal Medicine, Oklahoma State University Medical Center, Tulsa, USA.

Internal Medicine, Edward Via College of Osteopathic Medicine (VCOM) Carolinas, Spartanburg, USA.

出版信息

Cureus. 2025 Jan 9;17(1):e77196. doi: 10.7759/cureus.77196. eCollection 2025 Jan.

Abstract

Acute promyelocytic leukemia (APML) is a rare leukemia that leads to complications of renal toxicity, infections, leukocytosis, hemorrhaging, and disseminated intravascular coagulation, which is fatal. APML normally presents with bruising, bleeding, weakness, and infections. Patients can present with chest pain and shortness of breath due to coagulopathy. The workup for APML usually occurs when patients' labs return with leukocytosis and thrombocytopenia. Here, we report a case of a 75-year-old female with a past medical history of bronchiectasis, hypertension, and rheumatic fever who presented with chest pain and shortness of breath with elevated troponins and a normal EKG. The patient had worsened thrombocytopenia, leukocytosis, and an elevated D-dimer that did not resolve with steroids. The following report presents a patient diagnosed with APML with the initial symptoms of chest pain and shortness of breath without signs of acute coronary syndrome, leading to the diagnosis and treatment with ATRA.

摘要

急性早幼粒细胞白血病(APML)是一种罕见的白血病,可导致肾毒性、感染、白细胞增多、出血和弥散性血管内凝血等并发症,这些并发症是致命的。APML通常表现为瘀伤、出血、虚弱和感染。由于凝血功能障碍,患者可能会出现胸痛和呼吸急促。当患者实验室检查结果显示白细胞增多和血小板减少时,通常会对APML进行检查。在此,我们报告一例75岁女性病例,她有支气管扩张、高血压和风湿热病史,出现胸痛和呼吸急促,肌钙蛋白升高而心电图正常。该患者血小板减少、白细胞增多加重,D-二聚体升高,使用类固醇治疗后未缓解。以下报告介绍了一名被诊断为APML的患者,其最初症状为胸痛和呼吸急促,无急性冠状动脉综合征迹象,最终确诊并接受全反式维甲酸治疗。

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