Acute Erythroid Leukemia: A Rare Case Report

K. Akhtar, Sadaf Haiyat, A. Khan, B. Juneja, T. Khan, S. H. Arif
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Abstract

AML with myelodysplasia related changes is an uncommon type of acute myeloid leukemia. It comprises less than 5% of acute leukemias. According to the recent World Health Organization (WHO-2016) classification, AML cases with ≥ 50% or more erythroid cells and ≥ 20% total myeloblasts should be diagnosed as AML with myelodysplasia-related changes. Morphologic cellular features help to establish the diagnosis. We present a rare case of AML with myelodysplasia related changes in a 35-year-old female who presented with low-grade fever, mild epistaxis, and shortness of breath and diffuse sternal tenderness. The peripheral smear showed features of pancytopenia with 6% blasts along with evidence of hemolysis. Bone marrow examination revealed erythroid hyperplasia with 65% erythroblasts and 24% myeloblasts. Flow cytometry was used for the confirmation of the diagnosis. The patient was administered chemotherapy with Azacitidine 75 mg/m2/day × 7 days in IV infusion along with 2 units of red cell concentrate prophylactically to prevent anemia. Molecular studies are needed to understand better the pathogenesis of AML with myelodysplasiarelated changes and to develop newer diagnostic and prognostic markers.
急性红细胞白血病1例报道
AML伴骨髓异常增生相关改变是一种罕见的急性髓系白血病。它占急性白血病的不到5%。根据最近世界卫生组织(WHO-2016)的分类,红细胞≥50%及以上、总成髓细胞≥20%的AML患者应被诊断为AML伴骨髓增生异常相关改变。形态学细胞特征有助于确定诊断。我们报告一例罕见的AML伴骨髓增生异常相关改变的病例,患者为35岁女性,表现为低烧、轻度鼻出血、呼吸急促和弥漫性胸骨压痛。外周涂片显示全血细胞减少,伴6%原细胞,伴溶血。骨髓检查显示红系增生,红细胞增生65%,成髓细胞增生24%。流式细胞术用于确诊。给予阿扎胞苷75 mg/m2/天× 7天静脉滴注化疗,同时预防性使用红细胞浓缩物2单位预防贫血。分子研究需要更好地了解AML与骨髓增生异常相关变化的发病机制,并开发新的诊断和预后标志物。
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