Autoimmune Pancreatitis Type II: First Report from India

Autoimmune Pancreatitis (AIP) presents in two forms - Type I or lymphoplasmacytic sclerosing pancreatitis and Type II or idiopathic ducto-centric pancreatitis (IDCP). AIP II is rare in south Asia and, especially so, in India. Most patients have either Idiopathic Chronic Pancreatitis (ICP) or alcohol...

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Veröffentlicht in:Journal of clinical and diagnostic research 2017-09, Vol.11 (9), p.PD17-PD18
Hauptverfasser: Desai, Gunjan, Pande, Prasad, Tampi, Chandralekha, Wagle, Prasad
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Sprache:eng
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Zusammenfassung:Autoimmune Pancreatitis (AIP) presents in two forms - Type I or lymphoplasmacytic sclerosing pancreatitis and Type II or idiopathic ducto-centric pancreatitis (IDCP). AIP II is rare in south Asia and, especially so, in India. Most patients have either Idiopathic Chronic Pancreatitis (ICP) or alcohol related chronic pancreatitis. AIP Type I has been described in India. We herein report a patient who had features of ICP on imaging, for whom surgery was performed to relieve chronic pancreatic pain. However, the pathologic features revealed AIP Type II or IDCP.
ISSN:2249-782X
0973-709X
DOI:10.7860/JCDR/2017/29078.10664