[1] Abu-wasel B,Walsh C,Keough V,et al. Pathophysiology, epidemiology,classification and treatment options for polycystic liver diseases. World J Gastroenterol,2013,19(35):5775-5786. [2] Chandok N. Polycystic liver disease:a clinical review. Ann Hepatol,2012,11(6):819-826. [3] Torres VE,Harris PC,Pirson Y. Autosomal dominant polycystic kidney disease. Lancet,2007,369(9569):1287-1301. [4] Hogan MC,Masyuk TV,Page LJ,et al. Randomized clinical trial of long-acting somatostatin for autosomal dominant polycystic kidney and liver disease. J Am Soc Nephrol,2010,21(6):1052-1061. [5] Temmerman F,Missiaen L,Bammens B,et al. Systematic review: the pathophysiology and management of polycystic liver disease. Aliment Pharmacol Therapeut,2011,34(7):702-713. [6] Qian Q. Isolated polycystic liver disease. Adv Chron Kid Dis, 2010,17(2):181-189. [7] Peces R,González P,Venegas J. Enfermedad poliquística hepática no asociada a poliquistosis renal autosómica dominante. Nefrología,2003,23(5):454-458. [8] Lazaridis KN,Strazzabosco M,Larusso NF. The cholangiopathies: Disorders of biliary epithelia. Gastroenterology,2004,127(5): 1565-1577. [9] de la Piscina PR,Duca I,Estrada S,et al. Combined liver and kidney transplant in a patient with Budd-Chiari syndrome secondary to autosomal dominant polycystic kidney disease associated with polycystic liver disease:Report of a case with a 9-year follow-up. Gastrointestinal Med,2014,doi:10.1155/2014/585291. [10] Everson GT. Polycystic liver disease. Gastroenterol Hepatol, 2008,4(3):179-181. [11] Albandea moreno C,Aguilar urbano V,Fernández Pérez F, et al. Enfermedad poliquística hepática. Revista Espanola De Enfermedades Digestivas,2009,101(7):495-497. [12] Masoumi A,Reed-gitomer B,Kelleher C,et al. Developments in the management of autosomal dominant polycystic kidney disease. Therapeut Clin Risk Manag,2008,4(2):393-407. [13] Wilson SJ,Amsler K,Hyink DP,et al. Inhibition of Her-2 (neu/erbb2) restores normal function and structure to polycystic kidney disease(pkd) epithelia. Biochimica Et Biophysica Acta, 2006,1762(7):647-655. [14] Berthier CC,Wahl PR,Le hir M,et al. Sirolimus ameliorates the enhanced expression of metalloproteinases in a rat model of autosomal dominant polycystic kidney disease. Nephrol Dialysis Transplant,2008,23(3):880-889. [15] Walz G,Budde K,Mannaa M,et al. Everolimus in patients with autosomal dominant polycystic kidney disease. New Engl J Med,2010,363(9):830-840. [16] Renken C,Fischer D,Kundt G,et al. Inhibition of mtor with sirolimus does not attenuate progression of liver and kidney disease in Pck rats. Nephrol Dialys Transplant,2011,26(1):92-100. [17] Caroli A,Antiga L,Cafaro M,et al. Reducing polycystic liver volume in adpkd:Effects of somatostatin analogue octreotide. Clin J Am Soc Nephrol,2010,5(5):783-789. [18] Gevers TJ,Drenth JP. Somatostatin analogues for treatment of polycystic liver disease. Curr Opin Gastroenterol,2011,27(3): 294-300. [19] 林建军,金昌男,林圣远. 超声介入治疗非寄生虫性肝囊肿32例. 实用肝脏病杂志,2005,8(2):96-97. [20] 朱龙柏. 肝囊肿经腹腔镜开窗引流治疗的临床效果观察. 中国医药指南,2013,11(8):591-592. [21] Torres VE,Rastogi S,King BF,et al. Hepatic venous outflow obstruction in autosomal dominant polycystic kidney disease. J Am Soc Nephrol,1994,5(5):1186-1192. |