Skandrani K, Richardet J P, Duvoux C, Cherqui D, Zafrani E S, Dhumeaux D
Service d'Hépatologie et de Gastroentérologie, Hôpital Henri-Mondor, Créteil.
Gastroenterol Clin Biol. 1997;21(8-9):623-5.
We report a case of severe cholestasis and sicca syndrome after thiabendazole administration for Strongyloides stercoralis infection in a 26-year-old patient. Liver biopsy, performed 15 days after the onset of jaundice, revealed a marked paucity of bile ducts, and cholestasis rapidly progressed to biliary cirrhosis. Because of the progression of jaundice and the development of esophageal varices, orthotopic liver transplantation was performed, 18 months after the beginning of disease. The mechanism responsible for thiabendazole-induced biliary injury is unknown. The association between sicca syndrome and biliary disease suggests an immunoallergic mechanism against an antigen which could be common to the biliary, lacrimal and salivary duct epithelium.
我们报告了一例26岁患者在使用噻苯达唑治疗粪类圆线虫感染后出现严重胆汁淤积和干燥综合征的病例。黄疸出现15天后进行的肝活检显示胆管明显稀少,胆汁淤积迅速发展为胆汁性肝硬化。由于黄疸进展和食管静脉曲张的出现,在疾病开始18个月后进行了原位肝移植。噻苯达唑引起胆汁损伤的机制尚不清楚。干燥综合征与胆道疾病之间的关联提示了针对一种抗原的免疫过敏机制,该抗原可能是胆管、泪腺和唾液腺上皮所共有的。