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2020
Polycystic liver disease is a rare disease, manifesting with progressive bile duct enlargement and development of multiple cysts of various sizes in the liver. While it can be regarded as a hereditary disease, with either autosomal dominant transmission or autosomal recessive transmission, only about 20% of patients have been identified to have genetic
Carmen Fierbinteanu-Braticevici +1 more
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Polycystic liver disease is a rare disease, manifesting with progressive bile duct enlargement and development of multiple cysts of various sizes in the liver. While it can be regarded as a hereditary disease, with either autosomal dominant transmission or autosomal recessive transmission, only about 20% of patients have been identified to have genetic
Carmen Fierbinteanu-Braticevici +1 more
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Journal of Diagnostic Medical Sonography, 2004
As sonographic resolution capabilities improve and more abdominal sonograms are requested, diagnosis of polycystic liver disease (PLD) is on the increase. At first glance, the numerous liver cysts caused by PLD can be alarming. However, the disease is usually asymptomatic, and lab tests are generally within normal ranges.
Paula Rhodes, Sharon Aranda
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As sonographic resolution capabilities improve and more abdominal sonograms are requested, diagnosis of polycystic liver disease (PLD) is on the increase. At first glance, the numerous liver cysts caused by PLD can be alarming. However, the disease is usually asymptomatic, and lab tests are generally within normal ranges.
Paula Rhodes, Sharon Aranda
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Revue medicale suisse, 2022
Polycystic liver disease (PLD) includes three entities in adults : biliary hamartomas which develop as a result of ductal plate malformation, autosomal dominant polycystic liver disease (ADPLD) and autosomal dominant polycystic kidney disease (ADPKD) which occur in the setting of genetic disorders. Hamartomas are asymptomatic and benign. PLD are marked
Marie, Ongaro +4 more
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Polycystic liver disease (PLD) includes three entities in adults : biliary hamartomas which develop as a result of ductal plate malformation, autosomal dominant polycystic liver disease (ADPLD) and autosomal dominant polycystic kidney disease (ADPKD) which occur in the setting of genetic disorders. Hamartomas are asymptomatic and benign. PLD are marked
Marie, Ongaro +4 more
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Genetics of polycystic liver diseases
Current Opinion in Gastroenterology, 2019This review provides an outline of the most recent insights and significant discoveries regarding the genetic mechanisms involved in polycystic liver disease.Polycystic liver disease includes a heterogeneous group of genetic disorders characterized by multiple hepatic cysts. Isolated liver cysts are caused by mutations in Protein Kinase C Substrate 80K-
Lee-Law, Pui Y. +3 more
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JAMA, 1976
ABSTRACT POLYCYSTIC liver disease is a relatively rare condition with a reported autopsy incidence varying from 1/687 autopsies to 8/11, 245 autopsies.1-3 Ante-mortem diagnosis is usually made at surgery.4,5 It is the purpose of this report to discuss the noninvasive approach to the diagnosis of polycystic liver disease and to emphasize the role of ...
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ABSTRACT POLYCYSTIC liver disease is a relatively rare condition with a reported autopsy incidence varying from 1/687 autopsies to 8/11, 245 autopsies.1-3 Ante-mortem diagnosis is usually made at surgery.4,5 It is the purpose of this report to discuss the noninvasive approach to the diagnosis of polycystic liver disease and to emphasize the role of ...
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Cysts and Polycystic Liver Disease
2015Cystic and polycystic diseases are genetic and congenital disorders in which cysts occur in the liver (simple cysts and autosomal dominant polycystic liver disease) or in combination with cysts in the kidneys (autosomal dominant polycystic kidney disease). Women have a higher prevalence with a female-to-male ratio of 1.5:1.
GIULIANI, ANTONIO +5 more
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Liver Transplantation for Polycystic Liver Disease
Journal of the American College of Surgeons, 2014Daniel, Zamora-Valdés +2 more
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