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先天性肝纤维化合并lgG4相关性疾病1例报告

A case of congenital hepatic fibrosis with lgG4-related disease
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摘要 先天性肝纤维化(congenital hepatic fibrosis,CHF)诊断复杂,发病年龄以青少年为主,成人先天性肝纤维化发病较晚,通常以门静脉高压为主要临床表现,出血风险较高。成人CHF合并lg G4升高病例尚未见临床报道。为总结诊断和治疗CHF的经验,现报道如下。
作者 李正鑫 邢枫 周扬 陈高峰 刘成海 LI Zhengxin, XING Feng, ZHOU Yang, et al.(Institute of Liver Diseases, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China)
出处 《临床肝胆病杂志》 CAS 北大核心 2018年第10期2192-2194,共3页 Journal of Clinical Hepatology
关键词 先天性肝纤维化 免疫球蛋白G 活组织检查 病例报告 congenital hepatic fibrosis immunoglobulin G biopsy case reports
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