Abstract:
:Autoimmune pancreatitis (AIP) is defined as a particular form of pancreatitis that often manifests as obstructive jaundice associated with a pancreatic mass or an obstructive bile duct lesion, and that has an excellent response to corticosteroid treatment. The prevalence of AIP worldwide is unknown, and it is considered as a rare entity. The clinical and radiological presentation of AIP can mimic bilio-pancreatic cancer, presenting difficulties for diagnosis and obliging the surgeon to balance decision-making between the potential risk presented by the misdiagnosis of a deadly disease against the desire to avoid unnecessary major surgery for a disease that responds effectively to corticosteroid treatment. In this review we detail the current and critical points for the diagnosis, classification and treatment for AIP, with a special emphasis on surgical series and the methods to differentiate between this pathology and bilio-pancreatic cancer.
journal_name
Cir Espjournal_title
Cirugia espanolaauthors
Saavedra-Perez D,Vaquero EC,Ayuso JR,Fernandez-Cruz Ldoi
10.1016/j.ciresp.2014.01.013subject
Has Abstractpub_date
2014-12-01 00:00:00pages
645-53issue
10eissn
0009-739Xissn
1578-147Xpii
S0009-739X(14)00076-1journal_volume
92pub_type
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