Unusual Presentation of Primary Sclerosing Cholangitis
Author(s) -
BC Pineau,
LP Pattee,
Shan McGuire,
Arunkumar Sekar,
LJ Scully
Publication year - 1997
Publication title -
canadian journal of gastroenterology
Language(s) - English
Resource type - Journals
eISSN - 1916-7237
pISSN - 0835-7900
DOI - 10.1155/1997/948191
Subject(s) - medicine , primary sclerosing cholangitis , ankylosing spondylitis , ulcerative colitis , sacroiliitis , presentation (obstetrics) , gastroenterology , inflammatory bowel disease , autoimmune hemolytic anemia , hla b27 , autoimmune pancreatitis , pancreatitis , anemia , immunology , disease , human leukocyte antigen , surgery , antigen
A 23-year-old man presenting with acute pancreatitis and autoimmune hemolytic anemia was diagnosed with primary sclerosing cholangitis (PSC) without evidence of ulcerative colitis. This constellation of rare associations constitutes a unique mode of presentation of PSC. Within two years he also developed ankylosing spondylitis with sacroiliitis. Disordered immune regulation as a major factor in the mechanism of injury in PSC is supported by its increased association with other immunologically mediated disorders, most notably ulcerative colitis. Autoimmune hemolytic anemia, however, has been reported to be associated with PSC on only two occasions, and ankylosing spondylitis in the absence of ulcerative colitis is also unusual. In addition, the presentation of PSC with acute pancreatitis has rarely been described. This patient presented with several unusual features of PSC.
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