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References
Arnold HL, Harrison SA (2005) New advances in evaluation and management of patients with polycystic liver disease. Am J Gastroenterol 100: 2569–82
Bistritz L, Tamboli C, Bigam D, et al (2005) Polycystic liver disease: experience at a teaching hospital. Am J Gastroenterol 100: 2212–7
Caremani M, Vincenti A, Benci A, et al (1993) Ecographic epidemiology of non-parasitic hepatic cysts. J Clin Ultrasound 21: 115–8
Comfort MW, Gray HK, Dahlin DC, et al (1952) Polycystic disease of the liver: a study of 24 cases. Gastroenterology 20: 66–78
Cowles RA, Mulholland MW (2000) Solitary hepatic cysts. J Am Coll Surg 191: 311–21
Doty JE, Tompkins RK (1989) Management of cystic disease of the liver. Surg Clin N Am 69: 185–95
Drenth JP, Martina JA, Te Morsche RH, et al (2004) Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease. Gastroenter-ology 126: 1819–27
Everson GT, Taylor MRG, Doctor RB (2004) Polycystic disease of the liver. Hepatology 40: 774–82
Karhunen PJ, Tenhu M (1986) Adult polycystic liver and kidney diseases are separate entities. Clin Genet 30: 29–37
Kida T, Nakanuma Y, Terada T (1992) Cystic dilatation of peribiliary glands in livers with adult polycystic disease and livers with solitary nonparasitic cysts: an autopsy study. Hepatology 16: 334–40
Luoma PV, Sotaniemi EA, Ehnholm C (1980) Low high-density lipoprotein and reduced antipyrine metabolism in members of a family with polycystic liver disease. Scand J Gastroenterol 15: 869–73
Madariaga JR, Iwatsuki S, Starzl TE, et al (1993) Hepatic resection for cystic lesions of the liver. Ann Surg 218: 610–4
Melnick PJ (1954) Polycystic liver. Analysis of seventy cases. Arch Pathol Lab Med 59: 162–72
Milutinovic J, Fialkow PJ, Rudd TG, et al (1980) Liver cysts in patients with autosomal dominant polycystic kidney disease. Am J Med 68: 741–4
Nichols MT, Gidey E, Matzakos T, et al (2004) Secretion of cytokines and growth factors into autosomal dominant polycystic kidney disease liver cyst fluid. Hepatology 40: 836–46
Pirson Y, Lannoy N, Peters D, et al (1996) Isolated polycys-tic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2. Hepatology 23: 249–52
Que F, Nagorney D, Gross J Jr, et al (1995) Liver resection and cyst fenestration in the treatment of severe polycystic liver disease. Gastroenterology 108: 487–94
Qian Q, Li A, King BF, et al (2003) Clinical profile of auto-somal dominant polycystic liver disease. Hepatology 37: 164–71
Reynolds DM, Falk CT, Li AR (2000) Identification of a locus for autosomal dominant polycystic liver disease on chromosome 19p13.2–13.1. Am J Hum Genet 67: 1598–1604
Saini S, Mueller PR, Ferrucci JT Jr, et al (1983) Percutaneous aspiration of hepatic cysts does not provide definitive therapy. Am J Roentgenol 141: 559–60
Schievink WI, Spetzler RF (1998) Screening for intracranial aneurysms in patients with isolated polycystic liver disease. J Neurosurg 89: 719–21
Torres V, Rastogi S, King B, et al (1994) Hepatic venous outflow obstruction in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 5: 1186–92
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Dancygier, H. (2010). Liver Cysts and Polycystic Liver Disease. In: Clinical Hepatology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-04519-6_3
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