血栓性血小板减少性紫癜(Thrombtic thrombocytopenic purpura简称TTP),Moschcowitg于1952年首先描述,又称Moschcowitg综合征。本征甚为少见,临床经过凶险。我院于1986年收治一例,报告如下。患者王某、女性、32岁,于1986—05—17以血小板减少性紫癜入院。病人半月前头晕、头痛、发烧1 d,伴恶心、呕吐,不能进食,继之牙龈渗血、鼻衄,皮肤紫癜和淤斑。于当地医院就诊,曾用青霉素、氢考、维生素等,不见好转,症状进行性加重转来我院。患者既往健康。体检:体温36.5℃,脉搏80次/min,呼吸20次/min,血压110/80 Thrombotic thrombocytopenic purpura (TTP), Moschcowitg first described in 1952, also known as Moschcowitg syndrome. Very rare intrinsic, clinically dangerous. Our hospital admitted in 1986 a case, the report is as follows. Patient Wang, female, 32 years old, admitted to hospital with thrombocytopenic purpura on May 23, 1986. Half a month before the patient dizziness, headache, fever 1 d, with nausea, vomiting, can not eat, followed by gingival bleeding, epistaxis, purpura and ecchymosis. In the local hospital for treatment, once used penicillin, hydrogen test, vitamins, etc., did not improve, progressive symptoms increased to our hospital. The patient’s past health. Physical examination: body temperature 36.5 ℃, pulse 80 beats / min, breathing 20 beats / min, blood pressure 110/80