Results 111 to 120 of about 265,644 (234)

STAT1 Gain-of-Function with a Novel Clinical Manifestation: Recurrent Pancreatitis Associated with Hypertriglyceridemia and Anti-GPIHBP1 Autoantibodies

open access: yesJournal of Human Immunity
Patients with STAT1 gain-of-function (GOF) variants may present not only with chronic mucocutaneous candidiasis and other forms of immunodeficiency but also with a broad-spectrum of autoimmune manifestations, for which Janus kinase (JAK) inhibitors have ...
Areum Shin   +10 more
doaj   +1 more source

Cystic fibrosis transmembrane conductance regulator gene variants are associated with autoimmune pancreatitis and slow response to steroid treatment

open access: yes, 2017
Background: Autoimmune pancreatitis (AIP) is a distinct type of chronic pancreatitis. To date, the association of CFTR gene variants with AIP has not been studied. Methods: The entire coding and intronic regions of the CFTR gene were examined using next-
鄭永銘;詹一秀;翁昭旼;章明珠;田郁文;楊卿堯;張毓廷   +1 more
core   +1 more source

Autoimmune Pancreatitis: A Report from India [PDF]

open access: yes, 2010
Context Autoimmune pancreatitis is characterized by immune-mediated inflammation, prominent lymphocytic infiltration and fibrosis of pancreas. It accounts for 4.6-6% of chronic pancreatitis but only a few cases from India have been reported.
Noor, Mohd T   +10 more
core   +1 more source

PSC‐DM: A Validated Clinical Diagnostic Model for Distinguishing Primary From Secondary Sclerosing Cholangitis

open access: yesLiver International, Volume 46, Issue 11, November 2026.
ABSTRACT Background and Aims Primary sclerosing cholangitis (PSC) is a rare, progressive cholangiopathy for which diagnosis remains challenging because of the absence of disease‐specific markers and the presence of secondary causes of sclerosing cholangitis (SSC) that closely mimic its clinical presentation. Diagnostic uncertainty can delay appropriate
Miki Scaravaglio   +20 more
wiley   +1 more source

Drug cross-reactivity between methimazole and propylthiouracil causing recurrent pancreatitis in thyroid storm

open access: yesEndocrinology, Diabetes & Metabolism Case Reports
Drug-induced pancreatitis represents 1.1% of acute pancreatitis cases. To date, eight cases of antithyroid drug (ATD)-induced pancreatitis have been reported, including seven associated with methimazole (MMI) and one with carbimazole; however, no cases ...
Yuriko Yamazaki   +8 more
doaj   +1 more source

Kinin-B1 receptors in ischaemia-induced pancreatitis: Functional importance and cellular localisation [PDF]

open access: yes, 2003
In this study we compare the role of kininB1 and B2 receptors during ischaemia/reperfusion of rat pancreas. Our investigations were prompted by the observation that infusion of a kininB2 receptor antagonist produced significant improvement in acute ...
A. A. Roscher   +11 more
core   +1 more source

Diagnosis of autoimmune pancreatitis

open access: yesWorld Journal of Gastroenterology, 2014
Autoimmune pancreatitis (AIP) is a distinct form of chronic pancreatitis that is increasingly being reported. The presentation and clinical image findings of AIP sometimes resemble those of several pancreatic malignancies, but the therapeutic strategy differs appreciably. Therefore, accurate diagnosis is necessary for cases of AIP.
Hiroyuki, Matsubayashi   +6 more
openaire   +2 more sources

Severe Plasmodium vivax Malaria Complicated by Secondary Hemophagocytic Lymphohistiocytosis, Disseminated Intravascular Coagulation, and Acute Pancreatitis: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Plasmodium vivax (P. vivax) malaria, once regarded as a comparatively benign infection, is increasingly recognized as a cause of severe, potentially life‐threatening multisystem disease. Concurrent secondary hemophagocytic lymphohistiocytosis (HLH), disseminated intravascular coagulation (DIC), and acute pancreatitis complicating P.
Tasnim Nafian   +5 more
wiley   +1 more source

Autoimmune pancreatitis: problems and prospects

open access: yesSuizo, 2007
自己免疫性膵炎は本邦から疾患概念が提唱され,世界的にもこの疾患に対する認識が急速に高まりつつある.一方では,IgG4陽性形質細胞の膵への浸潤と血清IgG4高値を特徴とすることや,多彩な膵外病変を伴い全身疾患である可能性が提唱されるなど,疾患概念自体も変化してきており,なお流動的な側面を有している.病因や病態について今後明らかにされるべき多くの問題を抱えているが,特に臨床上早急にコンセンサスを要する点として,1)慢性膵炎の疾患概念における自己免疫性膵炎の位置づけ,2)自己免疫性膵炎の臨床病理学的な均一性,3)ステロイドによる診断的治療の是非,の3点を挙げたい.これらは,この疾患に関して臨床上混乱をきたす可能性のある大きな要因と考えられ,世界的にもより多くの専門家の間でコンセンサスが必要な問題である.
openaire   +2 more sources

Dorsal Pancreatic Agenesis Associated With New‐Onset Diabetes Mellitus and Acute Pancreatitis in an 18‐Year‐Old Man: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Dorsal pancreatic agenesis (DPA) is a rare congenital disorder resulting from failure of development of the dorsal pancreatic bud. Complete DPA implies absence of the pancreatic neck, body, and tail and can be associated with both diabetes mellitus and pancreatitis. The patient was an 18‐year‐old man admitted with a history of epigastric pain,
Mugheesa Rab   +5 more
wiley   +1 more source

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