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原发性胆汁性胆管炎合并非酒精性脂肪性肝炎一例 被引量：1

A case of primary biliary cholangitis with non-alcoholic steatohepatitis
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摘要 原发性胆汁性胆管炎(PBC)原名原发性胆汁性肝硬化,是器官特异性的慢性胆汁淤积性自身免疫性肝病[1]。PBC患者早期常有轻度乏力和间歇性瘙痒,半数患者有轻度肝肿大,血清碱性磷酸酶(ALP)和(或)γ-谷氨酰转肽酶(GGT)增高常为唯一阳性发现,也可有抗线粒体抗体(AMA)、抗核抗体(ANA)阳性;肝脏活组织病理检查可确诊,并可诊断疾病发展阶段及预测预后。
作者 何红梅 徐姝嫣 卞兆连 HE Hongmei;XU Shuyan;BIAN Zhaolian
机构地区 南通市第三人民医院消化内科
出处 《国际消化病杂志》 CAS 2021年第2期148-150,共3页 International Journal of Digestive Diseases
关键词 自身免疫性肝病 原发性胆汁性胆管炎 抗线粒体抗体 非酒精性脂肪性肝炎 活组织病理检查 阳性发现 原发性胆汁性肝硬化 轻度肝肿大
分类号 R57 [医药卫生—消化系统]
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国际消化病杂志
2021年 第2期

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