论文部分内容阅读
瑞氏综合征又称急性脑病合并内脏脂肪浸润综合征、呕吐病、肝脏脂质沉着症等,由澳大利亚医生 Reye 氏首次报道,迄今只有20多年的历史。本病发病急,死亡率高,主要危及儿童(3月～14岁),在我国及世界各地都有发生。为进一步探讨瑞氏综合征的临床和病理特点,我们对我院近13年来收集的41例瑞氏综合征尸检病例的临床和病理资料进行了复习,总结如下。材料和方法1972年12月至1985年10月,由我院及外院诊治并经尸体解剖检查证实的瑞氏综合征共41例(其中38例在我院诊治),常规取材,10%福
Reye’s syndrome, also known as acute encephalopathy with visceral fat infiltration syndrome, vomiting, liver lipidosis, etc., was first reported by the Australian doctor Reye’s, so far only 20 years of history. The incidence of acute disease, high mortality, the main endanger children (March to 14 years old), in our country and around the world have occurred. To further explore the clinical and pathological features of Wright’s syndrome, we reviewed the clinical and pathological data of 41 cases of Wright’s syndrome autopsy collected in our hospital in the past 13 years, and summarized as follows. Materials and Methods From December 1972 to October 1985, 41 patients with Wright’s syndrome (38 of them were diagnosed and treated in our hospital) were diagnosed by autopsy and confirmed by autopsy in our hospital from December 1972 to October 1985.