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血栓性血小板减少性紫癜(简称 TTP)是一种少见的综台征,其临床特点为血小板减少性紫癜,微血管病性溶血性贫血,中枢神经系统功能障碍及肾脏损害等。现将1例报告如下。郑××,男,31岁。因畏寒,发热、齿龈出血及皮肤紫癜20余天于1982年10月22日入院。10多年前因外伤致右眼失明。体检:T37℃,BP128/76mmHg,神志清楚,贫血外观。胸部及双下肢皮肤可见大量散在紫癜,巩膜轻度黄染。右眼外伤性白内障。心肺
Thrombotic thrombocytopenic purpura (referred to as TTP) is a rare syndrome, its clinical features of thrombocytopenic purpura, microangiopathic hemolytic anemia, central nervous system dysfunction and renal damage. Now one report is as follows. Zheng × ×, male, 31 years old. Due to chills, fever, bleeding gums and skin purpura more than 20 days in October 22, 1982 admitted. 10 years ago due to trauma to the right eye blindness. Physical examination: T37 ℃, BP128 / 76mmHg, conscious, anemic appearance. Chest and lower extremity skin visible a large number of scattered purpura, scleral mild yellow dye. Right eye traumatic cataract. Heart and lungs