Idiopathic Duct-Centric Pancreatitis (IDCP)
نویسندگان
چکیده
منابع مشابه
Simultaneous Presentation of Idiopathic Duct-Centric Pancreatitis and Ulcerative Colitis
A 22-year-old female with no significant past medical history was admitted with chronic bloody diarrhea and persistent epigastric pain radiating to the back for the previous 2 months. There was no history of nonsteroidal anti-inflammatory drugs or alcohol consumption. Physical examination revealed tenderness in the epigastrum, without peritoneal signs. Laboratory results showed leukocytosis (15...
متن کاملIdiopathic Duct Centric Pancreatitis in Korea: A Clinicopathological Study of 14 Cases
Autoimmune pancreatitis (AIP) is a distinct form of chronic pancreatitis, which has several autoimmune features such as elevated serum immunoglobulin levels and heavy lymphoplasmacytic infiltration. Two histological subtypes have been recently described: 1) lymphoplasmacytic sclerosing pancreatitis (LPSP) or type 1 AIP and 2) idiopathic duct centric pancreatitis (IDCP) or type 2 AIP. LPSP is ch...
متن کاملAutoimmune pancreatitis with histologically proven lymphoplasmacytic sclerosing pancreatitis with granulocytic epithelial lesions.
Recent histological and clinical studies have suggested the existence of 2 distinct types of autoimmune pancreatitis (AIP): type 1 AIP related to IgG4, exhibiting lymphoplasmacytic sclerosing pancreatitis (LPSP), and type 2 AIP related to granulocyte epithelial lesions (GELs), exhibiting idiopathic duct-centric chronic pancreatitis (IDCP). We herein present a case of type 1 AIP with histologica...
متن کاملHistopathologic and clinical subtypes of autoimmune pancreatitis: the Honolulu consensus document.
Autoimmune pancreatitis (AIP) has been extensively reported from Japan, Europe, and the United States. Whereas the descriptions of AIP from Japan have predominantly been based on the presence of a distinct clinical phenotype, reports from Europe and the United States describe at least 2 histopathologic patterns in patients' condition currently diagnosed as AIP, viz, lymphoplasmacytic sclerosing...
متن کاملRecent Advances in Autoimmune Pancreatitis.
Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis that is characterized clinically by frequent presentation with obstructive jaundice, histologically by a dense lymphoplasmacytic infiltrate with fibrosis, and therapeutically by a dramatic response to corticosteroid therapy. Two distinct diseases, type 1 and type 2 AIP, share these features. However, these 2 diseases have unique pa...
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ژورنال
عنوان ژورنال: Internal Medicine
سال: 2010
ISSN: 0918-2918,1349-7235
DOI: 10.2169/internalmedicine.49.4457