Singh Smita, Sharma Sunita, Tejwani Narender, Chandra Jagdish
Department of Pathology, Lady Hardinge Medical College & Associated Kalawati Saran Children Hospital, A-207, Narwana Appartments, Plot no. 89, I.P. Extension, New Delhi, 110092 India.
Indian J Hematol Blood Transfus. 2012 Sep;28(3):184-6. doi: 10.1007/s12288-011-0117-8. Epub 2011 Oct 18.
Idiopathic myelofibrosis a disease of elderly is rarely seen in children. A case of chronic idiopathic myelofibrosis in an 8 year old boy with Down's syndrome is reported here, who presented with progressive pallor and hepatosplenomegaly. Peripheral blood examination revealed pancytopenia, macrocytic anemia and tear drop cells. No blasts were found. Bone marrow aspirate yielded a dry tap and trephine biopsy showed marrow fibrosis with osteosclerosis. Focally megakaryocytes were increased in number with atypical morphology. No blasts were seen. Review of literature revealed 47 reported cases of childhood idiopathic myelofibrosis. Six cases were associated with Down's syndrome and only 3 of them had features of chronic idiopathic myelofibrosis without evidence of acute megakaryoblastic leukaemia.
原发性骨髓纤维化是一种多见于老年人的疾病,在儿童中很少见。本文报道了一例患有唐氏综合征的8岁男孩的慢性原发性骨髓纤维化病例,该男孩表现为进行性面色苍白和肝脾肿大。外周血检查显示全血细胞减少、大细胞性贫血和泪滴状细胞。未发现原始细胞。骨髓穿刺呈干抽,骨髓活检显示骨髓纤维化伴骨硬化。局部巨核细胞数量增加且形态异常。未见到原始细胞。文献回顾显示,有47例儿童原发性骨髓纤维化的报道。6例与唐氏综合征相关,其中只有3例具有慢性原发性骨髓纤维化的特征,且无急性巨核细胞白血病的证据。