Uncommon localization of amyloidosis in gallbladder: Description of a case and brief literature review
Journal Title: Annals of Hepatology - Year 2011, Vol 10, Issue 2
Abstract
Amyloidosis is a rare disease that is caused by extracellular deposits of amorphous, insoluble fibrillar protein, which often occur in the kidneys, the heart, the nervous system, the digestive tract, especially the hepatosplenic and intestinal tract, and can be present in bone marrow, though unusual in the gallbladder. The interest of this case lies in the rarity of amyloidosis localisation and in the uncommon clinical presentation as acute cholecystitis. We have reviewed cases of amyloidosis with gallbladder involvement in literature and briefly discussed thepredictive value of the main histological diagnostic methods.
Authors and Affiliations
Daniela Tirotta, Vittorio Durante
Epidemiology and natural history of non-alcoholic fatty liver disease (NAFLD)
[b][/b]The authors summarize and update the most recent knowledge in the field of prevalence, natural history and incidence of Non Alcoholic Fatty Liver Disease (NAFLD) and Non Alcoholic Steatohepatitis (NASH). These nov...
Can ARFI elastography predict the presence of significant esophageal varices in newly diagnosed cirrhotic patients?
Aim. To establish an algorithm which includes the liver stiffness (LS) and/or spleen stiffness (SS) assessed by ARFI for the prediction of significant esophageal varices-EV (at least grade 2). Material and methods. Our...
Multiple Biliary Hamartomas, The ‘‘Von Meyenburg Complexes’’
-
The socioeconomic impact of hepatitis C infection and liver transplantation in Mexico
Efficacy of telaprevir-based therapy in stable liver transplant patients with chronic genotype 1 hepatitis C
Background and rationale. The REPLACE study (NCT01571583) investigated telaprevir-based triple therapy in patients whohave recurrent genotype 1 hepatitis C virus (HCV) infection following liver transplantation and are o...