Results 21 to 30 of about 265,644 (234)
Internal Medicine, 2005 Although the pathogenesis of autoimmune pancreatitis is unclear, recent evidence of clinical aspects are presented: (i) mild abdominal symptoms, usually without acute attacks of pancreatitis; (ii) occasional existence of obstructive jaundice; (iii) increased levels of serum gammaglobulin, IgG or IgG4; (iv) presence of autoantibodies; (v) diffuse ...
OKAZAKI, Kazuichi +3 more
+10 more sources
Hepatology, EarlyView., 2022 NRPT 1X reduces ALT and ceramide 14:0 in 65% of subjects as compared to only 28% in the placebo group. Abstract Background and Aims The prevalence of NAFLD is increasing globally and on a path to becoming the most frequent cause of chronic liver disease. Strategies for the prevention and treatment of NAFLD are urgently needed.
Ryan W. Dellinger +7 more
wiley +1 more source
Caracterització dels tipus d'activació de diferents poblacions de macròfags durant la pancreatitis aguda experimental i la seva relació amb la severitat del procés [PDF]
, 2011 Malgrat els esforços dedicats a investigar la pancreatitis aguda (PA), segueixen sense resposta la major part de les preguntes plantejades fa anys. En particular, encara no es coneixen tots els mecanismes pels que una lesió localitzada en el pàncrees pot
Gea Sorli, Sabrina
core +7 more sources
Journal of Gastroenterology and Hepatology, 2011 AbstractThe purpose of this review is to provide a concise view of the existing knowledge of autoimmune pancreatitis (AIP) for practicing clinicians. AIP is a rare disease whose recognition and understanding are evolving. It is a type of chronic pancreatitis that often presents as obstructive jaundice, has a distinctive histology, and is exquisitely ...
Aravind, Sugumar, Suresh T, Chari
openaire +2 more sources
Biomedical Papers, 2014 Autoimmune pancreatitis (AIP) is the specific type of chronic pancreatitis due to autoimmune background and mechanism.The main clinical symptoms of AIP are obstructive jaundice and abdominal discomfort. The typical histological findings are lymphocytes and IgG4 plasma cells infiltration, fibrosis and venulitis within pancreatic gland.
Petr, Dite +5 more
openaire +2 more sources
Two Siblings with Type 1 Autoimmune Pancreatitis [PDF]
, 2013 Type 1 autoimmune pancreatitis (AIP) is characterized by a high serum IgG4 concentration and is closely associated with the HLA-DRB1*04:05-DQB1*04:01 haplotype, for which family studies may disclose its immunogenetic significance.
Ito, Tetsuya +9 more
core +1 more source
Characteristic findings in images of extra-pancreatic lesions associated with autoimmune pancreatitis [PDF]
, 2010 Purpose: Autoimmune pancreatitis is a unique form of chronic pancreatitis characterized by a variety of extra-pancreatic involvements which are frequently misdiagnosed as lesions of corresponding organs.
Kadoya, Masumi +9 more
core +1 more source
Mechanisms of Lower Bile Duct Stricture in Autoimmune Pancreatitis [PDF]
, 2014 Objectives We attempted to clarify the mechanism underlying lower bile duct stricture in autoimmune pancreatitis. Methods Imaging and histologic finding of the bile duct were assessed for 73 patients with autoimmune pancreatitis to clarify whether IgG4 ...
Arakura, Norikazu +17 more
core +1 more source
Gland Surgery, 2016 Autoimmune pancreatitis (AIP) is a rare, distinct and increasingly recognized form of pancreatitis which has autoimmune features. The international consensus diagnostic criteria (ICDC) for AIP recently described two subtypes; type 1[lymphoplasmacytic sclerosing pancreatitis (LPSP)] and type 2 [idiopathic duct-centric pancreatitis (IDCP) or AIP with ...
openaire +2 more sources
Autoimmune Pancreatitis with Extreme Elevation of DUPAN-2 [PDF]
, 2007 An 80-year-old woman was admitted to our hospital with complaints of jaundice and liver dysfunction. She was found to have a high titer of serum IgG4, positive rheumatoid factor and marked elevation of DUPAN-2 (11,148 U/ml).
Masuda, Jun-ich +12 more
core +1 more source