Abstract
Autoimmune pancreatitis is characterised by diffuse enlargement of pancreas, narrowing of pancreatic duct, lymphoplasmacytic infiltrations and fibrosis. The disease is responsive to corticosteroid. We report the case of a 32year-old male who presented with unilateral exophthalmos and obstructive jaundice secondary to pancreatic head mass and biliary tract stricture. Serum immunoglobulin G level was raised with a very high immunoglobulin G4 subclass. Ophthalmological imaging revealed unilateral thickening of extraocular muscles. The patient responded well to corticosteroid with resolution of biliary strictures, pancreatic head mass and exophthalmos.
Original language | English |
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Pages (from-to) | 1125-1127 |
Number of pages | 3 |
Journal | Journal of the Pakistan Medical Association |
Volume | 65 |
Issue number | 10 |
Publication status | Published - Oct 2015 |
Externally published | Yes |
Keywords
- Autoimmune pancreatitis
- Exophthalmos
- IgG4-related systemic disease