Knott A W, Ampudia R J, Evankovich C, Teplick S K, Herrera J L, Tucker J A, Rodning C B
Department of Internal Medicine, University of South Alabama, Mobile, USA.
South Med J. 2000 Jul;93(7):698-702.
Intrahepatic nonparasitic cystic disease is rare and may be of congenital or neoplastic origin. The most frequent symptoms and signs are nonspecific and include pain, nausea, fullness, increased girth, and palpable mass. Interventional therapy is reserved for symptomatic patients, which usually corresponds to cysts >5 cm in diameter. Retrospective analysis revealed 26 cases of intrahepatic cystic disease over 15 years at our institution. We discuss the case of a patient who had bilobular biliary cystadenomatous disease, a rare, benign variant of intrahepatic nonparasitic cystic disease.
肝内非寄生虫性囊性疾病较为罕见，可能源于先天性或肿瘤性。最常见的症状和体征不具有特异性，包括疼痛、恶心、饱胀感、腹围增加以及可触及的肿块。介入治疗适用于有症状的患者，通常指直径大于5厘米的囊肿。回顾性分析显示，我们机构在15年间共出现26例肝内囊性疾病。我们讨论了一例患有双叶胆管囊腺瘤病的患者，这是肝内非寄生虫性囊性疾病中一种罕见的良性变体。
