Results 11 to 20 of about 31,827 (245)
Co-Occurrence of Neurofibromatosis Type 1 and Polycystic Liver Disease: A Case of Hypertension with PKHD1 Variant. [PDF]
Am J Case RepThewjitcharoen Y +5 more
europepmc +2 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 ...
Albandea Moreno,C. +5 more
+9 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: Advances in Understanding and Treatment. [PDF]
Annu Rev Pathol, 2022 Masyuk TV, Masyuk AI, LaRusso NF.
europepmc +3 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 disease [PDF]
BMJ Case Reports, 2014 A widespread use of ultrasound (US) examination is contributing to an increase in the diagnosis of renal and hepatic cysts. However, the vast majority of these lesions are benign with an indolent course during the patient's lifespan. Adult polycystic kidney disease (APKD) is one of the most common diagnosed entities.
Rodrigo Nazário, Leão +2 more
openaire +2 more sources
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 +2 more sources
Molecular Mechanisms of Isolated Polycystic Liver Diseases
Frontiers in Genetics, 2022 Polycystic liver disease (PLD) is a rare autosomal dominant disorder including two genetically and clinically distinct forms: autosomal dominant polycystic kidney disease (ADPKD) and isolated polycystic liver disease (PCLD).
Ziqi Yu +5 more
doaj +1 more source