论文部分内容阅读
骨髓纤维化是一种骨髓增生性的疾病,以红细胞、粒细胞等系列的异常增生,不同程度的骨髓纤维组织增生及肝脾的髓外化生为特征。本病较少见,国内仅见零星报道。国外文献统计发病以50～70岁为多见,儿童罕见。我院于1985年6月收治一例,报告如下: 患儿男,4(1)/2岁,镇江人,因脸色苍黄20余天,伴不规则发热于1985年6月12日入院。无出血,大小便正常。系第一胎第一产,足月顺产,母乳喂养,周岁断奶。无特殊药物史,也无放射线接触史。体检:发育中等,
Myelofibrosis is a myeloproliferative disease characterized by abnormal proliferation of erythrocytes and granulocytes, varying degrees of myelofibrosis and extrahepatic metaplasia of liver and spleen. The disease is rare, only sporadic domestic reports. The incidence of foreign literature statistics to 50 to 70 years of age is more common, children are rare. In our hospital in June 1985 admitted to a case, the report is as follows: Children male, 4 (1) / 2 years old, Zhenjiang, pale face due to more than 20 days, with irregular fever admitted on June 12, No bleeding, normal urine. Department of the first birth of the first child, term full-term, breast-feeding, wearable age. No special drug history, no history of radiation exposure. Physical examination: developing medium,