Polycystic Liver Disease: A Case Report

R. Adiwinata, Natalin Allorerung, Jonathan Arifputra, Andrea Livina, P. Lasut, B. J. Waleleng, Fandy Gosal, Luciana Rotty, Jeanne Winarta, Andrew Waleleng, M. Tendean
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Abstract

Polycystic liver disease is characterized by multiple cystic lesions on the liver. Liver cysts are typically incidental findings, with occasional complications including cyst hemorrhage, infection and rupture. Polycystic liver disease may be part of autosomal dominant polycystic liver disease (ADPLD). Autosomal dominant polycystic liver disease is considered rare autosomal dominant disease, with prevalence of 1/100,000-1,000,000. Without family history of polycystic liver disease, ADPLD is defined as the presence of more than 20 liver cysts with no renal cysts, however up to third of ADPLD may have small number of renal cysts without kidney function impairment. This case of a 73-year-old woman with symptomatic polycystic liver disease, and we performed cyst fenestration-deroofing via laparoscopic.
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多囊性肝病1例报告
多囊性肝病的特点是肝脏出现多个囊性病变。肝囊肿通常是偶然发现的,偶有并发症,包括囊肿出血、感染和破裂。多囊性肝病可能是常染色体显性多囊性肝病(ADPLD)的一部分。常染色体显性多囊性肝病被认为是罕见的常染色体显性疾病,患病率为1/100,000-1,000,000。无多囊性肝病家族史的ADPLD定义为有20个以上的肝囊肿而无肾囊肿,但高达三分之一的ADPLD可能有少量的肾囊肿而无肾功能损害。本病例是一名73岁女性多囊性肝病的症状,我们通过腹腔镜进行囊肿开窗清除。
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