论文部分内容阅读
血栓性血小板减少性紫癜(简称TTP)是一少见疾病,常易误诊,作者所见两例,报告如下: 例一:邓×、女、21岁、未婚、工人、住院号262388、1983年12月12日入院。八三年七月,始有两膝关节游走性疼痛、行动受限,按“风湿”在厂医院治疗五天,服强地松症状消失而出院。至八月份感乏力、厌油、纳差、肝功有异,按“肝炎”住院治疗、症状无改善。九月份始发热、咳嗽、伴肌肉酸痛、时有吐、于10月26日住某院治疗。三天后全身出紫癜,体温达39—40℃,用安比西林静点及服强地
Thrombotic thrombocytopenic purpura (referred to as TTP) is a rare disease, often misdiagnosed, the authors see two cases, the report is as follows: Example 1: Deng ×, female, 21 years old, unmarried, workers, hospital number 262388, 1983 12 On the 12th admission. In July 1983, two knees began to have painful sexual intercourse and their mobility was limited. According to “Rheumatism”, they were treated in the hospital for five days, and their symptoms of prednisone disappeared and discharged. To August a sense of fatigue, tired of oil, anorexia, different liver function, according to “hepatitis” hospitalized, no improvement in symptoms. September was fever, cough, with muscle soreness, sometimes vomiting, on October 26 to live in a hospital for treatment. Three days after the body purpura, body temperature of 39-40 ℃, with ampicillin static points and convincing