Recent advances in the diagnosis and management of autoimmune pancreatitis

Ashish Khandelwal; Alampady Krishna Shanbhogue; Naoki Takahashi; Kumaresan Sandrasegaran; Srinivasa R. Prasad

doi:10.2214/AJR.13.11247

Recent advances in the diagnosis and management of autoimmune pancreatitis

Ashish Khandelwal, Alampady Krishna Shanbhogue, Naoki Takahashi, Kumaresan Sandrasegaran, Srinivasa R. Prasad

Research output: Contribution to journal › Review article › peer-review

29 Scopus citations

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	https://doi.org/10.2214/AJR.13.11247
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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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.",

keywords = "Autoimmune pancreatitis, International consensus diagnostic criteria, Pancreas, Pancreatitis, Type 1 autoimmune pancreatitis, Type 2 autoimmune pancreatitis",

author = "Ashish Khandelwal and Shanbhogue, {Alampady Krishna} and Naoki Takahashi and Kumaresan Sandrasegaran and Prasad, {Srinivasa R.}",

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AU - Shanbhogue, Alampady Krishna

AU - Takahashi, Naoki

AU - Sandrasegaran, Kumaresan

AU - Prasad, Srinivasa R.

PY - 2014/5

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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

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KW - Type 1 autoimmune pancreatitis

KW - Type 2 autoimmune pancreatitis

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Recent advances in the diagnosis and management of autoimmune pancreatitis

Abstract

Keywords

ASJC Scopus subject areas

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