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Chronic myeloid leukemia presenting with absence of basophils and marked dyspoiesis.

机译:慢性粒细胞白血病,缺乏嗜碱性粒细胞和明显的营养不良。

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A 61-year old woman presented to us with fever, weakness and ecchymotic patches for one year. She had leucocytosis, anemia and thrombocytopenia. Peripheral blood smear showed 62% neutrophils, 32% myelocytes and metamyelocytes, 2% promyelocytes, 1% blasts, 2% monocytes, 1% lymphocytes but no basophils and marked dyspoiesis. Bone marrow picture was essentially the same. A diagnosis of atypical chronic myeloid leukemia was suggested. The correct diagnosis of chronic myeloid leukemia-accelerated phase was, however, made on cytogenetic analysis which showed Philadelphia chromosome (Ph) and isochromosome 17q [i(17q)]. This case describes a rare and diagnostically difficult presentation of CML arising out of a combination of prominent dyspoiesis and near absence of peripheral blood basophils.
机译:一名61岁的女性向我们展示了发烧,无力和瘀斑一年。她患有白细胞增多症,贫血和血小板减少症。外周血涂片显示62%的中性粒细胞,32%的骨髓细胞和间质细胞,2%的早幼粒细胞,1%的母细胞,2%的单核细胞,1%的淋巴细胞,但没有嗜碱性粒细胞和明显的营养不良。骨髓图片基本相同。建议诊断为非典型慢性粒细胞白血病。然而,通过细胞遗传学分析可以正确诊断慢性粒细胞白血病加速期,该分析显示了费城染色体(Ph)和等染色体17q [i(17q)]。该病例描述了CML的罕见和诊断困难表现,这是由显着的营养不良和几乎没有外周血嗜碱性粒细胞引起的。

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