Popov M S, Rutkovskiĭ O V
Arkh Patol. 1982;44(4):60-3.
An observation of primary biliary hepatocirrhosis with granulomatous reaction in a woman of 50 is presented. The disease for 3 years was accompanied by hepatic cholestasis. Diagnostic laparotomy done to exclude the mechanical nature of cholestasis revealed cholecystolithiasis, and cholecystectomy was performed. The material of marginal intraoperational liver biopsy revealed chronic nonsuppurative destructive cholangitis, proliferation of biliary tubules and periductullar fibrosis, granulomas containing giant multinuclear cells of Pirogov-Langhans type, and morphological signs of chronic active hepatitis.
本文报告了一名50岁女性原发性胆汁性肝硬变伴肉芽肿反应的病例。该疾病3年来伴有肝内胆汁淤积。为排除胆汁淤积的机械性病因进行了诊断性剖腹手术,发现有胆囊结石,并实施了胆囊切除术。术中肝边缘活检材料显示为慢性非化脓性破坏性胆管炎、胆小管增生及管周纤维化、含有皮罗果夫-朗汉斯型巨大多核细胞的肉芽肿以及慢性活动性肝炎的形态学表现。