Highlights
- •XGP is a very rare form of chronic pancreatitis and in a majority of cases is misdiagnosed as a primary pancreatic neoplasm.
- •XGP can present as a solid or a cystic lesion and typically shows hypoattenuation on CT, high T2 signal, and low T1 signal.
- •XGP is often FDG-avid on PET and can show increased FDG uptake throughout or at the periphery—corresponding to wall uptake.
- •A relatively thick and enhancing wall is usually identified which has an infiltrative appearance about half of the time.
- •XGP should be considered when a pancreatic mass has an infiltrative appearing wall and involves surrounding structures.
Abstract
Xanthogranulomatous pancreatitis (XGP) is an extremely rare cause of a cystic pancreatic
mass. The pathophysiology of this process is not entirely clear but likely results
from a combination of duct obstruction, infection, and repeated hemorrhage. It is
difficult to differentiate this inflammatory lesion from a cystic neoplasm and, therefore,
in the majority of cases XGP is misdiagnosed as a neoplasm on preoperative imaging.
In this report, we describe a case of XGP, the imaging characteristics of XGP, and
a differential diagnosis for a cystic pancreatic lesion.
Keywords
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Article info
Publication history
Published online: May 23, 2017
Accepted:
May 22,
2017
Received in revised form:
May 21,
2017
Received:
March 10,
2017
Identification
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