Results 11 to 20 of about 50,700 (248)
Liver Transplantation for Polycystic Liver Disease [PDF]
Archives of Surgery, 1990 Four female patients with severe complications of polycystic liver disease were treated with liver replacement; two patients were also given kidneys from their liver donors. All four of the patients were suffering from extreme fatigue.
Gordon, R +5 more
core +4 more sources
Management of Polycystic Liver Disease [PDF]
Canadian Journal of Gastroenterology, 2004 Polycystic liver disease (PCLD) is characterized by multiple cysts throughout the liver. Patients may develop chronic intractable symptoms that may be debilitating. Others may develop medical complications that necessitate intervention.
Justin Cheung +2 more
doaj +3 more sources
Polycystic disease of the liver [PDF]
Hepatology, 2004 Autosomal dominant polycystic disease is genetically heterogeneous with mutations in two distinct genes predisposing to the combination of renal and liver cysts (AD-PKD1 and AD-PKD2) and mutations in a third gene yielding isolated liver cysts (the polycystic liver disease gene).
Gregory T. Everson +2 more
openalex +5 more sources
Combined liver-kidney transplant in polycystic diseases: a case report [PDF]
Einstein (São Paulo), 2023 Polycystic liver disease, a hereditary pathology, usually manifests as autosomal dominant polycystic kidney disease. The many cysts in the liver cause massive hepatomegaly, majorly affecting the patient’s quality of life. In cases of refractory symptoms,
Olival Cirilo Lucena da Fonseca Neto +7 more
doaj +1 more source
Severe polycystic liver disease in a cat. [PDF]
JFMS Open Rep, 2023 Case summary Ductal plate malformations (DPMs) are poorly documented in the veterinary literature, particularly those of the polycystic liver disease (PCLD) phenotype. A 13-year-old female spayed cat presented with progressive icterus, abdominal distension, weight loss and elevated liver enzymes.
King EM +5 more
europepmc +4 more sources
Polycystic liver disease [PDF]
Revista Española de Enfermedades Digestivas, 2009 A 54-year-old man had an asymptomatic elevation of cytolysis-related enzymes, GGT, and alkaline phosphatase, detected at a routine laboratory study. The patient reported no alcohol abuse, no history of liver disease, and no constitutional syndrome. Physical examination showed a good general status, normal colored skin and mucosas, and no stigmata of ...
A. Sánchez Cantos +5 more
openaire +5 more sources
Polycystic Liver Disease: A Case Report
The Indonesian Journal of Gastroenterology, Hepatology and Digestive Endoscopy, 2021 Polycystic liver disease is characterized by multiple cystic lesions on the liver. Liver cysts are typically incidental findings, with occasional complications including cyst hemorrhage, infection and rupture.
Randy Adiwinata +10 more
doaj +1 more source
Polycystic liver disease: an overview of clinical manifestations, diagnosis, and treatment [PDF]
Kosin Medical Journal, 2023 Polycystic liver disease (PLD) is a hereditary disease characterized by the presence of 20 or more liver cysts. It is classified into three types: isolated autosomal dominant PLD, PLD with autosomal dominant polycystic kidney disease, and PLD with ...
Joonho Jeong, Hyun Joon Park
doaj +1 more source
Polycystic liver diseases [PDF]
Digestive and Liver Disease, 2010 Polycystic liver diseases (PCLDs) are genetic disorders with heterogeneous etiologies and a range of phenotypic presentations. PCLD exhibits both autosomal or recessive dominant pattern of inheritance and is characterized by the progressive development of multiple cysts, isolated or associated with polycystic kidney disease, that appear more extensive ...
ONORI, PAOLO +7 more
openaire +3 more sources
An Empirical Biomarker-based Calculator for Autosomal Recessive Polycystic Kidney Disease - The Nieto-Narayan Formula [PDF]
, 2016 Autosomal polycystic kidney disease (ARPKD) is associated with progressive enlargement of the kidneys fuelled by the formation and expansion of fluid-filled cysts.
Goldberg, Itzhak D. +3 more
core +10 more sources