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Transient Acute Myeloid Leukemia in a Newborn with Down?s Syndrome

机译:唐氏综合征新生儿的短暂性急性髓细胞白血病

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We report the case of a newborn with Down's syndrome associated with transient acute myeloid leukemia (AML). The leukemic presentation resolved spontaneously without treatment just 4 weeks after birth. A 2 days old newborn presented with respiratory distress, lethargy, poor suck and mild hepatosplenomegaly with features of Down's syndrome. Total white cell count was 144,000/cmm with blasts 92%. Other Septic work up was negative. Peripheral blood smear revealed hyper leukocytosis and presence of blast cells. Flow cytometric analysis revealed acute myeloid leukemia. The peripheral blast cells persisted for 4 weeks, after which the hemogram and the differential WBC count returned to normal and a final diagnosis of transient acute myeloid leukemia was made. Only few cases of congenital leukemia with Down's syndrome have been reported in the literature. In Down's syndrome, AML whether transient or not, generally shows cytogenetic and molecular aspects that differ from those of adult acute leukemiasJ Bangladesh Coll Phys Surg 2016; 34(4): 213-217
机译:我们报告了唐氏综合症与短暂性急性髓细胞性白血病(AML)相关的新生儿的病例。出生后仅四个星期,白血病症状未经治疗即自动消退。 2天大的新生儿表现出呼吸窘迫,嗜睡,吮吸不良和轻度肝脾肿大,并伴有唐氏综合症。白细胞总数为144,000 / cmm,爆炸率为92%。其他化粪池检查结果为负面。外周血涂片显示白细胞增多和原始细胞的存在。流式细胞仪分析显示急性髓性白血病。外周母细胞持续4周,此后血象图和WBC差异计数恢复正常,并最终诊断为短暂性急性髓细胞性白血病。文献中仅报道了先天性唐氏综合症白血病病例。在唐氏综合症中,AML(无论是否短暂)通常显示出不同于成人急性白血病的细胞遗传学和分子学方面的内容(J Bangladesh Coll Phys Surg 2016; 2011)。 34(4):213-217

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