Abstract
OBJECTIVE. Autoimmune pancreatitis (AIP) is a rare chronic relapsing steroid-responsive fibroinflammatory disorder of the pancreas that is likely caused by immune dysregulation. It is now thought that AIP consists of two distinct clinicopathologic syndromes currently designated as types 1 and 2. CONCLUSION. A current update on etiopathogenesis, pathology, and clinical and imaging findings of AIP is provided with an emphasis on diagnosis and management.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1007-1021 |
| Number of pages | 15 |
| Journal | American Journal of Roentgenology |
| Volume | 202 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 2014 |
Keywords
- Autoimmune pancreatitis
- International consensus diagnostic criteria
- Pancreas
- Pancreatitis
- Type 1 autoimmune pancreatitis
- Type 2 autoimmune pancreatitis
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging
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Cite this
Khandelwal, A., Shanbhogue, A. K., Takahashi, N., Sandrasegaran, K., & Prasad, S. R. (2014). Recent advances in the diagnosis and management of autoimmune pancreatitis. American Journal of Roentgenology, 202(5), 1007-1021. https://doi.org/10.2214/AJR.13.11247