论文部分内容阅读
原发性血小板减少性紫癜(ITP),系一种常见的出血性疾病,本文分析我院1976～1985年收治的82例ITP病例,探讨骨髓巨核细胞象改变对ITP的诊断意义。一、临床资料:82例诊断标准按1984年全国血液病会议提出的标准。其中年龄最小3个月,最大66岁,25岁以下64例;男性42例,女性40例;病程最短1天,最长12年,1个月以内38例,6个月以内56例;急性型29例,慢性型53例。其中81例均有皮下出血,且为就诊的首要症状;粘膜下出血以鼻衄、牙龈
Primary thrombocytopenic purpura (ITP) is a common hemorrhagic disease. This article analyzes 82 cases of ITP treated in our hospital from 1976 to 1985 to investigate the significance of the changes of bone marrow megakaryocytes in the diagnosis of ITP. First, the clinical data: 82 cases of diagnostic criteria by the 1984 national blood disease meeting proposed standards. Among them, the youngest 3 months, the oldest 66 years old, 64 cases under the age of 25; 42 males and 40 females; duration of the shortest 1 day, up to 12 years, 38 months within 1 month, 56 cases within 6 months; acute 29 cases, 53 cases of chronic type. Among them, 81 cases had subcutaneous hemorrhage, and the most important symptom of treatment; submucosal hemorrhage with epistaxis, gums