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. 2014 Aug 18;8(5):462–470. doi: 10.5009/gnl14107

Table 3.

Subtypes of Autoimmune Pancreatitis

Subtype of AIP Type 1 Type 2
Other nomenclatures AIP without GEL AIP with GEL
IgG4-related IgG4-unrelated
LPSP IDCP
Prevalence Asia>USA, EU EU>USA>Asia
Age High aged Younger
Gender Male>>Female Male=Female (NS)
Symptoms
 Obstructive jaundice Often Often
 Abdominal pain Rare Common
Pancreas swelling Common Common
Serology High serum IgG, IgG4, autoAbs (+) Normal IgG, normal IgG4, autoAbs (−)
OOI Sclerosing cholangitis Unrelated with OOI
Sclerosing sialadenitis
Reteroperitoneal fibrosis
Others
Ulcerative colitis Rare Often
Steroid Responsive Responsive
Relapse High rate Rare

AIP, autoimmune pancreatitis; GEL, granulocytic epithelial lesion; LPSP, lymphoplasmacytic sclerosing pancreatitis; IDCP, idiopathic duct-centric chronic pancreatitis; NS, not significant; OOI, other organ involvement.