Acute Promyelocytic Leukemia and Chronic Lymphocytic Leukemia: Concomitant Presentation of Two Molecularly Distinct Entities.

Jingdong Su, Diana Veillon, Rodney Shackelford, James Cotelingam, Hazem El-Osta, Glenn Mills, Reinhold Munker, Srinivas Devarakonda
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Abstract

Acute myeloid leukemia (AML) developing in patients with chronic lymphocytic leukemia (CLL) is very uncommon and usually associated with prior treatment. Acute promyelocytic leukemia (APL) accounts for a very small proportion of treatment-associated AML. So far, there has been only one reported case of APL occurring post radiation for prostate cancer in a patient with CLL. We report herein the first case of APL and CLL presenting concomitantly in an untreated patient. Evaluation of peripheral blood and bone marrow aspirate with immunohistochemistry, flow cytometry, and FISH to confirm two morphologically, molecularly and genetically distinct leukemic populations characteristic of APL and CLL is required. APL is a hematologic emergency, and aggressive management is vital to a successful therapeutic outcome. Standard treatment is with All-trans retinoic acid (ATRA) and anthracycline-based regimen, whether the process is de novo or therapy-related. Due to increased incidence of secondary malignancies in CLL patients, active surveillance is necessary.

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急性早幼粒细胞白血病和慢性淋巴细胞白血病:两种不同分子实体的同时表现。
急性髓性白血病(AML)在慢性淋巴细胞白血病(CLL)患者中发展是非常罕见的,通常与既往治疗有关。急性早幼粒细胞白血病(APL)占治疗相关AML的很小比例。到目前为止,只有一例慢性淋巴细胞白血病患者在前列腺癌放疗后发生APL。我们在此报告第一例APL和CLL同时出现在未经治疗的患者。需要用免疫组织化学、流式细胞术和FISH对外周血和骨髓抽吸物进行评估,以确认APL和CLL两种形态、分子和遗传上不同的白血病群体特征。APL是一种血液急症,积极的治疗对成功的治疗结果至关重要。标准治疗是全反式维甲酸(ATRA)和以蒽环类药物为基础的方案,无论该过程是从头开始还是与治疗相关。由于CLL患者继发恶性肿瘤的发生率增加,主动监测是必要的。
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