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Polycystic Liver Disease: Pathophysiology, Diagnosis and Treatment [PDF]
Hepatic Medicine: Evidence and Research, 2022 Luiz Fernando Norcia,1 Erika Mayumi Watanabe,2 Pedro Tadao Hamamoto Filho,3 Claudia Nishida Hasimoto,1 Leonardo Pelafsky,1 Walmar Kerche de Oliveira,1 Ligia Yukie Sassaki4 1Department of Surgery, São Paulo State University (Unesp), Medical School ...
Norcia LF +6 more
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Polycystic liver disease: a clinical review
Annals of Hepatology, 2012 Polycystic liver disease rarely occurs in isolation as part of autosomal dominant polycystic liver disease, but more commonly, it exists as an extra-renal manifestation of autosomal dominant polycystic kidney disease. The pathogenesis of polycystic liver
Natasha Chandok, M.D., MPH, FRCPC
doaj +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
Isolated Polycystic Liver Disease
Acta Médica Portuguesa, 2017 N/A.
Rita Seara Costa +2 more
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The pathophysiology of polycystic liver disease
Journal of HepatologyContains fulltext : 306407.pdf (Publisher’s version ) (Open Access)
Tom J G Gevers, Melissa M Boerrigter
exaly +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
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 ...
Albandea Moreno,C. +5 more
+8 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
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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
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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
openaire +4 more sources