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Ulcerative Colitis, Autoimmune Hemolytic Anemia and Primary Sclerosing Cholangitis in a Child
Author(s) -
Susan Gilmour,
Peter Chait,
Melinda Phillips,
Eve A. Roberts
Publication year - 1996
Publication title -
canadian journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
eISSN - 2291-2797
pISSN - 2291-2789
DOI - 10.1155/1996/762589
Subject(s) - autoimmune hemolytic anemia , ulcerative colitis , medicine , primary sclerosing cholangitis , inflammatory bowel disease , vitiligo , pathogenesis , immunology , alopecia areata , gastroenterology , anemia , autoimmune disease , incidence (geometry) , disease , physics , optics
A 15-month-old female who initially presented with autoimmune hemolytic anemia (AIHA) is described. She developed bloody stools and was diagnosed with ulcerative colitis (UC). Investigations of persistent hepatomegaly revealed primary sclerosing cholangitis (PSC). The association of AIHA, UC and PSC has never been reported. All these conditions entail impaired immunoregulation. Patients with a clustering of autoimmune diseases may help to delineate the pathogenesis of UC. Autoimmune phenomena may be prominent in inflammatory bowel disease. UC, in particular, exhibits a high incidence of associated autoimmune diseases including hypothyroidism, PSC, vitiligo and alopecia areata. AIHA is well described in 0.5% to 1.0% of adult UC patients but has not been reported in children with UC

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