韦格内氏肉芽肿(Wegner’s Granulomatosis)是一种罕见而又严重的疾病。其发病年龄多在40岁以上,国内仅有少数病例报道,小儿病例更为罕见。现将所见的一例经尸检证实的儿童病例报告于后。患儿女,11岁,学生,住院号17758。于1976年2月11月入院。患者于入院前两月开始高热、头痛、鼻衄、音哑、口咽疼痛及溃烂,用青、链霉素治疗无效,以“疑似白喉”于1976年1月3日首 Wegner’s Granulomatosis is a rare and serious disease. The age of onset more than 40 years of age, only a few cases of domestic reports, more rare cases of children. A case of confirmed childhood autopsy will be reported later. Children with children, 11 years old, student, hospital number 17758. In February 1976 admitted to hospital in November. Patients began fever, headache, epistaxis, dumbness, oropharyngeal pain and ulceration two months before admission. Treatment with streptomycin and streptomycin was ineffective and “suspected diphtheria” was first placed on January 3, 1976