Diagnosis of autoimmune pancreatitis

doi:10.3748/wjg.v20.i44.16559

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Nov 28, 2014 (publication date) through Aug 24, 2024

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World Journal of Gastroenterology

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1007-9327

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World J Gastroenterol. Nov 28, 2014; 20(44): 16559-16569
Published online Nov 28, 2014. doi: 10.3748/wjg.v20.i44.16559

Table 5 Characteristics of clinicopathological findings in type 1 and type 2 autoimmune pancreatitis

	Type 1 AIP	Type 2 AIP
Geographical distributuion	Asia > United States, Europe	Europe > United States > Asia
Age at presentation	60-70 s	40-50 s
Gender	Male >> Female	Male = Female
Symptoms	Jaundice, Abdominal pain	Jaundice, Abdominal pain
Serology	IgG4, IgG, Autoantibodies	Usually negative
Pancreatic images	Enlarged (focal, diffuse)	Enlarged (focal, diffuse)
Pancreatic histology	LPSP	IDCP with GEL
Extrapancreatic lesions	Sclerosing cholangitis, sialoadenitis, retroperitoneal fibrosis, interstitional nephritis, etc.	Inflammatory bowel disease
Steroid response	Excellent	Excellent
Relapse	High rate	Rare

AIP: Autoimmune pancreatitis; LPSP: Lymphoplasmacytic sclerosing pancreatitis; IDCP with GEL: Idiopathic duct-centritic pancreatitis with granulocyte epithelial lesion.

Citation: Matsubayashi H, Kakushima N, Takizawa K, Tanaka M, Imai K, Hotta K, Ono H. Diagnosis of autoimmune pancreatitis. World J Gastroenterol 2014; 20(44): 16559-16569
URL: https://www.wjgnet.com/1007-9327/full/v20/i44/16559.htm
DOI: https://dx.doi.org/10.3748/wjg.v20.i44.16559