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Published on: May 29, 2020
Autoimmune pancreatitis associated with IgG4-related cholangitis: A radiologic-serologic correlation
Chorouk Mountassir1, Romaissaa Boutachali1, Feryal El Oualladi1
1Department of Radiology, Ibn Rochd University Hospital, Casablanca, Morocco.
Abstract:
Autoimmune pancreatitis (AIP) is a rare fibro-inflammatory disease that may closely mimic pancreatic malignancy, making accurate diagnosis challenging. We report the case of a 42-year-old man presenting with acute epigastric pain, elevated serum lipase levels, and imaging initially suggestive of acute interstitial pancreatitis. Magnetic resonance imaging revealed diffuse pancreatic enlargement with diffusion restriction, a peripheral capsule-like rim, and a tapered stenosis of the main pancreatic duct, associated with circumferential thickening of the bile duct walls and upstream intrahepatic bile duct dilatation. These imaging findings raised the suspicion of type 1 AIP associated with IgG4-related cholangitis. The diagnosis was confirmed by elevated serum IgG4 levels. This case highlights the importance of correlating characteristic pancreatic and biliary imaging features with serological findings to avoid misdiagnosis and unnecessary surgical management.
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Pancreatitis is the inflammation of the pancreas, which occurs when the immune system becomes active and causes swelling, pain, and disruptions in organ function. Pancreatitis can manifest as either an acute or chronic condition.
Acute pancreatitis arises suddenly and lasts for a brief duration, while chronic pancreatitis is a long-term affliction...
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Acute pancreatitis is characterized by rapid inflammation of the pancreas, often caused by factors like gallstone blockage or excessive alcohol consumption. Chronic pancreatitis, on the other hand, is a slow, progressive inflammation that may result from long-term alcohol abuse, obstructions in the pancreatic duct, or genetic factors.
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