Autoimmune Pancreatitis
TYPE-1 Autoimmune Pancreatitis
What is type-1 autoimmune pancreatitis in the framework of an IgG4-related disease?
Lymphoplasmacytic sclerosing pancreatitis as part of a systemic fibroinflammatory disease that may affect several organs (liver, kidneys, lungs, etc.).
How is it diagnosed?
Type-1 autoimmune pancreatitis manifests itself mainly in men (80% of cases) ages 50 and over. Revealing symptoms may include obstructive jaundice secondary to a cephalic pancreatic mass or the presence of cholangitis (intrapancreatic or diffuse cholangitis of the biliary tree). Other symptoms may include clear alteration of general health, with diabetic decompensation, anorexia and weight loss, thus mimicking pancreatic adenocarcinoma. As an IgG4-type disease, complications involving other organs (whether synchronous or metachronous) are present in more than 50% of cases. The patient may thus show symptoms of these extrapancreatic complications.
Imaging is used to establish the autoimmune origin (heterogeneity of the pancreatic parenchyma, peripancreatic halo, loss of pancreatic lobulations with “sausage” appearance, irregular diameter of the main pancreatic duct, tumour-like appearance). Other organs may be affected (cholangitis, retroperitoneal fibrosis, etc.).
The serum IgG4 level is high (> 1.35 g/L or more than twice the normal level) in most cases.
A pancreatic biopsy, if performed, will reveal a lymphoplasmacytic infiltrate and the presence of plasmacytes strongly expressing the anti-IgG4 antibody.
What is its specific treatment?
In case of symptoms, treatment is based on corticosteroids (40 mg/day) for one month, followed by progressive decrease in dosage. In case of resistance to or dependence on corticosteroids, treatment with immunomodulators should be discussed in a specialised centre.
Recommendations on IgG4 diseases: United European Gastroenterology (UEG) Webinar
Follow the UEG webinar presenting the new management recommendations for IgG4 pathologies by:
Jonas ROSENDAHL and Matthias LÖHR (Internal Medicine I, Martin Luther University of Halle, Germany)
and Vinciane REBOURS (Pancreaty Service, Beaujon Hospital, Clichy, University of Paris, France)TYPE-2 Autoimmune Pancreatitis
What is type-2 autoimmune pancreatitis?
Pancreatitis that is secondary to destruction of ductal epithelial cells via infiltration of neutrophilic polynuclear compounds.
How is it diagnosed?
Type-2 autoimmune pancreatitis manifests itself mainly as acute, isolated and benign pancreatitis. The sex ratio is one to one, and symptoms generally begin to appear at around age 40. Twenty to thirty percent of patients have a related chronic inflammatory bowel disease (IBD). The serum IgG4 level is normal.
Imaging is used to establish the autoimmune origin (heterogeneity of the pancreatic parenchyma, peripancreatic halo, loss of pancreatic lobulations with “sausage” appearance, irregular diameter of the main pancreatic duct).
A pancreatic biopsy, if performed, will reveal destruction of the ductal epithelial cells by infiltration of neutrophilic polynuclear compounds.
Diagnosis can be complex to perform. It is rare to obtain histological proof after puncture of the pancreas and revelation of a granulocytic epithelial lesion (GEL, a characteristic histological lesion). Diagnosis is thus based on the combination of morphological criteria by X-ray, the presence of related IBD and response to treatment with corticosteroids.
What is its specific treatment?
In case of symptoms, treatment is based on corticosteroids (40 mg/day) for one month, followed by progressive decrease in dosage. In case of resistance to or dependence on corticosteroids, treatment with immunomodulators should be discussed.
Source: Reference Centre for Rare Pancreatic Diseases and Disorders
Relevant reference centre: PaRaDis
