Results 281 to 290 of about 50,269 (316)
Some of the next articles are maybe not open access.
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.
Birgitte Brun, Jørn Palbøl
openaire +3 more sources
Diagnosis and management of polycystic liver disease
Nature Reviews Gastroenterology & Hepatology, 2013Polycystic 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) and as an extrarenal manifestation in autosomal dominant polycystic kidney disease (ADPKD).
Gevers, T.J.G., Drenth, J.P.H.
openaire +4 more sources
Liver transplantation for adult polycystic liver disease
Liver Transplantation and Surgery, 1996Patients with adult polycystic liver disease and massive cystic replacement of the liver may present with severe debilitation and impairment of functional performance or, rarely, with signs of portal hypertension or hepatic dysfunction. In those patients incapacitated by severe hepatomegaly secondary to massive cystic replacement with predominantly ...
William Kenneth Washburn +3 more
openaire +3 more sources
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
openaire +3 more sources
Orthotopic Liver Transplantation in Polycystic Liver Disease
Cirugía Española (English Edition), 2013There is currently no effective medical therapy for polycystic liver (PCL). Cyst puncture and sclerotherapy, cyst fenestration, or partial hepatic resections have been used as palliative treatments. Orthotopic liver transplantation (OLT) has become the treatment of choice for terminal PCL, being indicated in patients with limiting symptoms not ...
Jorge Arredondo +7 more
openaire +3 more sources
Polycystic Liver Disease in Autosomal Dominant Polycystic Kidney Disease
Global Journal of Gastroenterology & Hepatology, 2016Liver cysts are a commonly encountered phenomenon and may represent a broad cluster of disorders of diverse etiology. Most cysts are asymptomatic and do not require treatment. Simple cysts are the most prevalent. Polycystic liver disease (PLD) can be diagnosed when more than 20 cysts are detected in the liver.
Mariusz Niemczyk +2 more
openaire +2 more sources
Liver Transplantation for Polycystic Liver Disease
New England Journal of Medicine, 2007A 51-year-old woman with polycystic liver and kidney disease had undergone renal transplantation 21 years before presentation. She had no evidence of cerebrovascular malformations. Both her father and aunt also had polycystic kidney disease. After the renal transplantation, her liver had become progressively diseased and enlarged through cystic changes.
openaire +2 more sources
POLYCYSTIC DISEASE OF THE LIVER
Australian and New Zealand Journal of Surgery, 1953Norman Waddle, Roland Rodda
openaire +3 more sources
Onconephrology: The intersections between the kidney and cancer
Ca-A Cancer Journal for Clinicians, 2021Mitchell H Rosner +2 more
exaly