Childhood Myelodysplastic Syndrome: A Rare Entity

Mavra Fatima
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Abstract

Myelodysplastic syndrome (MDS) is a spectrum of bone marrow disorders resulting from clonal stem cell defect that manifest as cytopenias, ineffective hematopoiesis and dysplasia in all the three cell lines. Myelodysplastic syndrome is rare in children and accounts for less than 5% of the hematopoieitic malignancies below the age of 14 years. Refractory cytopenia of childhood (RCC) is the most common type of MDS that is seen in children. In this study, we report a case of 14 years old boy who presented to us with suspicion of aplastic anemia and was diagnosed as refractory cytopenia of childhood, a type of myelodysplastic syndrome.
儿童骨髓增生异常综合征:一个罕见的实体
骨髓增生异常综合征(MDS)是由克隆干细胞缺陷引起的一系列骨髓疾病,表现为三种细胞系的细胞减少、造血功能低下和发育不良。骨髓增生异常综合征在儿童中很少见,占14岁以下造血恶性肿瘤的不到5%。儿童期难治性细胞减少症(RCC)是儿童中最常见的MDS类型。在这项研究中,我们报告了一个14岁的男孩,他向我们提出了再生障碍性贫血的怀疑,并被诊断为儿童期难治性细胞减少症,一种骨髓增生异常综合征。
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