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 |
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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
Cite this
Recent advances in the diagnosis and management of autoimmune pancreatitis. / Khandelwal, Ashish; Shanbhogue, Alampady Krishna; Takahashi, Naoki; Sandrasegaran, Kumaresan; Prasad, Srinivasa R.
In: American Journal of Roentgenology, Vol. 202, No. 5, 05.2014, p. 1007-1021.Research output: Contribution to journal › Review article
}
TY - JOUR
T1 - Recent advances in the diagnosis and management of autoimmune pancreatitis
AU - Khandelwal, Ashish
AU - Shanbhogue, Alampady Krishna
AU - Takahashi, Naoki
AU - Sandrasegaran, Kumaresan
AU - Prasad, Srinivasa R.
PY - 2014/5
Y1 - 2014/5
N2 - 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.
AB - 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.
KW - Autoimmune pancreatitis
KW - International consensus diagnostic criteria
KW - Pancreas
KW - Pancreatitis
KW - Type 1 autoimmune pancreatitis
KW - Type 2 autoimmune pancreatitis
UR - http://www.scopus.com/inward/record.url?scp=84899535655&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84899535655&partnerID=8YFLogxK
U2 - 10.2214/AJR.13.11247
DO - 10.2214/AJR.13.11247
M3 - Review article
C2 - 24758653
AN - SCOPUS:84899535655
VL - 202
SP - 1007
EP - 1021
JO - American Journal of Roentgenology
JF - American Journal of Roentgenology
SN - 0361-803X
IS - 5
ER -