Ulcerative colitis, autoimmune hemolytic anemia and primary sclerosing cholangitis in a child

被引:7
|
作者
Gilmour, SM
Chait, P
Phillips, MJ
Roberts, EA
机构
[1] Hospital for Sick Children, University of Toronto, Toronto, Ont.
[2] Div. of Gastroenterol. and Nutrition, Hospital for Sick Children, Toronto, Ont. M5G 1X8
来源
CANADIAN JOURNAL OF GASTROENTEROLOGY | 1996年 / 10卷 / 05期
关键词
autoimmune hemolytic anemia; autoimmune phenomena; child; primary sclerosing cholangitis; ulcerative colitis;
D O I
10.1155/1996/762589
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:301 / 303
页数:3
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