Results 191 to 200 of about 39,270 (221)
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Autoimmune Pancreatitis

Digestive Diseases and Sciences, 2017
Autoimmune pancreatitis (AIP) is a chronic fibroinflammatory disease of the pancreas that belongs to the spectrum of immunoglobulin G-subclass4-related diseases (IgG4-RD) and typically presents with obstructive jaundice. Idiopathic duct-centric pancreatitis (IDCP) is a closely related but distinct disease that mimics AIP radiologically but manifests ...
Shounak, Majumder   +2 more
openaire   +2 more sources

Autoimmune pancreatitis

ANZ Journal of Surgery, 2002
The recommended treatment for a focal mass in the head of the pancreas is pancreaticoduodenectomy. Preoperative biopsy is not advised in patients who are candidates for resection because of the documented risk of tumour dissemination along the needle tract and significant false negative results.1 Autoimmune pancreatitis is a relatively uncommon ...
Mehrdad, Nikfarjam   +4 more
openaire   +2 more sources

Autoimmune pancreatitis mimicking pancreatic cancer

Journal of Hepato-Biliary-Pancreatic Sciences, 2009
Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis that can often be difficult to distinguish from pancreatic cancer. We describe the clinical and radiographic features of 23 patients with AIP whose presentations mimicked pancreatic cancer.A review of clinic, radiology, and endoscopy records from a 6-year period identified patients with ...
Lindsay S, Robison   +5 more
openaire   +2 more sources

Autoimmune Chronic Pancreatitis

The American Journal of Gastroenterology, 2004
In recent years a peculiar type of chronic pancreatitis with underlying autoimmunity has been described. Lymphoplasmacytic infiltration and fibrosis on histology and elevated IgG levels or detected autoantibodies on laboratory data support the concept of autoimmune chronic pancreatitis (AIP).
Kyu-Pyo, Kim   +5 more
openaire   +2 more sources

Autoimmune Pankreatitis

Der Internist, 2009
Autoimmune pancreatitis has been established as a special entity of pancreatitis. It is an enigmatic disease since it is adding an autoimmune etiology to the existing causes of pancreatitis. Morphological hallmarks of the disease are narrowing of the pancreatic duct system and the bile duct by periductal lymphoplasmocytic inflammation.
A, Schneider, J M, Löhr
openaire   +2 more sources

Autoimmune Pankreatitis

Zeitschrift für Gastroenterologie, 2002
Over the last years several case reports and articles have been published suggesting that a new form of chronic pancreatitis has been diagnosed and named autoimmune pancreatitis. The present overview scrutinizes the proposed evidence in the light of the current literature and aims to prove whether autoimmune pancreatitis is a special entity of chronic ...
M, Rünzi   +4 more
openaire   +2 more sources

Diagnosing autoimmune pancreatitis with the Unifying-Autoimmune-Pancreatitis-Criteria

Pancreatology, 2017
We had developed the Unifying-Autoimmune-Pancreatitis-Criteria (U-AIP) to diagnose autoimmune pancreatitis (AiP) within the M-ANNHEIM classification of chronic pancreatitis. In 2011, International-Consensus-Diagnostic-Criteria (ICDC) to diagnose AiP have been published. We had applied the U-AIP long before the ICDC were available. The aims of the study
Alexander Schneider   +15 more
openaire   +2 more sources

Pancreatic islet autoimmunity

La Presse Médicale, 2012
Type 1 diabetes (T1D) represents 10 to 15% of all forms of diabetes. Its incidence shows a consistent rise in all countries under survey. Evidence for autoimmunity in human T1D relies on the detection of insulitis, of islet cell antibodies, of activated β-cell-specific T lymphocytes and on the association of T1D with a restricted set of class II major ...
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Autoimmune pancreatitis

Gastrointestinal Endoscopy, 2004
Terumi, Kamisawa   +2 more
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[Autoimmune pancreatitis].

La Revue du praticien, 2015
There are two types of autoimmune pancreatitis. Type 1 is a part of a polyexocrinopathy syndrome associated with an elevation of serum igG4. Other organs might be involved: salivary glands, biliary ducts, retroperitoneum, kidneys, etc. Relapse risk is elevated and evolution to exocrine and endocrine insufficiencies is possible.
Vinciane, Rebours, Philippe, Lévy
openaire   +1 more source

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