Atypical morphology and aberrant immunophenotypic expression: A diagnostic dilemma in acute promyelocytic leukemia

Q4 Medicine
Shipra Verma, Paresh Singhal, Sharanjit Singh, Satyaranjan Das
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引用次数: 3

Abstract

Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia, which is highly aggressive, yet the most curable. It is a medical emergency that requires a very high index of suspicion, as delay in the treatment could lead to fatality. The initial diagnosis is made on the basis of its typical clinical presentation, morphological and immunophenotypic features. However, definitive diagnosis rests on the cytogenetic study. We present one such interesting case of APL where the morphology as well as immunophenotypic features was quite deceiving, leading to a diagnostic dilemma.
非典型形态和异常免疫表型表达:急性早幼粒细胞白血病的诊断困境
急性早幼粒细胞白血病(APL)是急性髓系白血病的一种亚型,具有高度侵袭性,但最容易治愈。这是一种需要高度怀疑的医疗紧急情况,因为延误治疗可能导致死亡。根据其典型的临床表现、形态学和免疫表型特征进行初步诊断。然而,最终的诊断取决于细胞遗传学研究。我们提出了一个有趣的APL病例,其形态学和免疫表型特征非常具有欺骗性,导致诊断困境。
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来源期刊
Journal of Applied Hematology
Journal of Applied Hematology Medicine-Hematology
CiteScore
0.40
自引率
0.00%
发文量
34
审稿时长
24 weeks
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