先天性无胆囊者临床罕见,笔者接诊及尸检一例,现报告如下: 患儿男,3个月,生后进行性皮肤巩膜黄染,大便呈陶土色。当地乡卫生院曾查肝功能诊为“新生儿肝炎”,治疗二月无效。皮下肌注处流血不止,伴阵发性尖叫及抽搐二天转来本院。 Congenital absence of gallbladder are clinically rare, the author admissions and autopsy in one case, are as follows: Children, 3 months after birth, the scleral skin sclerosis, stool color was clay. Local township hospitals have checked liver function diagnosed as “neonatal hepatitis”, treatment February invalid. Subcutaneous muscle injection at the bleeding, with paroxysmal screaming and convulsions transferred to the hospital two days.