Cavanzo F J, Garcia C F, Botero R C
Department of Pathology, Fundación Santa Fé de Bogotá, Colombia.
Gastroenterology. 1990 Sep;99(3):854-6. doi: 10.1016/0016-5085(90)90980-f.
The unique case of severe chronic cholestasis with paucity of bile ducts accompanied by pure red cell aplasia and the Stevens-Johnson syndrome in a 35-year-old woman after ampicillin ingestion is presented. The patient improved gradually and is asymptomatic 4 years later. Sequential histological and clinical follow-up substantiate the course of her disease.
本文报告了一例35岁女性在服用氨苄西林后出现严重慢性胆汁淤积伴胆管稀少，并伴有纯红细胞再生障碍和史蒂文斯-约翰逊综合征的独特病例。患者逐渐好转，4年后无症状。连续的组织学和临床随访证实了她的病程。
