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Polycystic Kidney/Liver Disease
Clinics in Liver Disease, 2022Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder that leads to chronic kidney disease and end-stage kidney disease (ESKD). Polycystic liver disease (PCLD) is the most common extrarenal manifestation of ADPKD. Though isolated PCLD and PCLD due to ADPKD are genetically distinct, they follow a similar clinical course of ...
Douglas T Dieterich +2 more
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Diagnosis and management of polycystic liver disease
Nature Reviews Gastroenterology and Hepatology, 2013 Item does not contain fulltextPolycystic liver disease (PLD) is arbitrarily defined as a liver that contains >20 cysts. The condition is associated with two genetically distinct diseases: as a primary phenotype in isolated polycystic liver disease (PCLD)
Tom J G Gevers
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Polycystic liver disease: ductal plate malformation and the primary cilium
Trends in Molecular Medicine, 2014 Item does not contain fulltextPolycystic livers are found in autosomal dominant polycystic kidney disease (ADPKD), caused by polycystic kidney disease (PKD)1 and PKD2 mutations in virtually all cases, and in isolated polycystic liver disease (PCLD ...
Ronald Roepman, Edgar S Wills
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Polycystic Disease of the Liver
Acta Radiologica. Diagnosis, 1977Three cases of the syndrome of polycystic disease of the liver and kidneys are present. The definite diagnoses were established by means of angiography. Exploratory laparotomy was avoided. The incidence and symptoms of the syndrome and the diagnostic potentials of the methods of examination are reviewed.
B, Brun, J, Palbol
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1996
Abstract The term ‘Polycystic liver disease’ (PLO) is often used to describe a condition with numerous cysts scattered throughout the liver parenchyma (Poinso et al. 1954; Melnick 1955; Peltokallio 1970; Sanfelippo et al. 1974; Vauthey et al. 1991).
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Abstract The term ‘Polycystic liver disease’ (PLO) is often used to describe a condition with numerous cysts scattered throughout the liver parenchyma (Poinso et al. 1954; Melnick 1955; Peltokallio 1970; Sanfelippo et al. 1974; Vauthey et al. 1991).
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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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Management of polycystic liver disease
Current Gastroenterology Reports, 2005The adult forms of polycystic liver disease are characterized by autosomal dominant inheritance and numerous hepatic cysts, with or without renal involvement. Mutations in two distinct genes predispose to renal and liver cysts (PKD1 and PKD2), and mutations in two different genes yield isolated liver cysts (PRKCSH and SEC63).
Gregory T, Everson, Matthew R G, Taylor
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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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