首页> 外文期刊>International Journal of Applied and Basic Medical Research >The paradox of recurrent with rare: A rare case of bilateral proptosis and facial palsy in acute myeloid leukemia with recurrent cytogenetic translocation t(8:21)
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The paradox of recurrent with rare: A rare case of bilateral proptosis and facial palsy in acute myeloid leukemia with recurrent cytogenetic translocation t(8:21)

机译:复发与罕见的悖论:急性髓样白血病中双侧眼突和面神经麻痹的罕见病例,复发性细胞遗传学易位t(8:21)

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摘要

A 13-year-old female child presented with bilateral proptosis and subconjuctival hemorrhage of 2 months duration. Subsequently, the biopsy and peripheral smears confirmed the diagnosis of acute myeloid leukemia (AML). Recurrent cytogenetic translocation t(8:21) in AML associated with extramedullary manifestation; was discovered which is a rare event. Furthermore, myeloperoxidase negative blasts and periodic acid Schiff negative blasts in AML with t(8:21) is a very rare combination to the best of our knowledge.Keywords: Acute myeloid leukemia, bilateral proptosis, cytogenetics
机译:一名13岁女童出现双侧突眼和结膜下出血,病程2个月。随后,活检和外周涂片证实了急性髓细胞性白血病(AML)的诊断。 AML中与髓外表现相关的复发性细胞遗传易位t(8:21);被发现是罕见的事件。此外,据我们所知,AML中t(8:21)的髓过氧化物酶阴性母细胞和高碘酸Schiff阴性母细胞是非常罕见的组合。关键词:急性髓细胞性白血病,双侧眼突,细胞遗传学

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