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一名免疫缺陷儿童的乳头狭窄和硬化性胆管炎。

Papillary stenosis and sclerosing cholangitis in an immunodeficient child.

作者信息

Gremse D A, Bucuvalas J C, Bongiovanni G L

机构信息

Children's Hospital Research Foundation, University of Cincinnati College of Medicine, Ohio.

出版信息

Gastroenterology. 1989 Jun;96(6):1600-3. doi: 10.1016/0016-5085(89)90533-7.

Abstract

Sclerosing cholangitis, an inflammatory disease of the biliary tree that occurs infrequently in childhood, has been recognized in combination with papillary stenosis in adults with the acquired immunodeficiency syndrome. A 10-yr-old child with a familial immunodeficiency syndrome characterized by defective T-cell function and deficiencies of immunoglobulins A and G developed papillary stenosis and sclerosing cholangitis associated with cryptosporidium enteritis. The patient presented with fever, jaundice, right upper quadrant pain, and elevated serum concentrations of transaminases and alkaline phosphatase. The pain and jaundice resolved after endoscopic sphincterotomy, but the biochemical abnormalities persisted. This case demonstrates that the combination of papillary stenosis and sclerosing cholangitis can occur in children as well as adults and may be associated with immunodeficiency syndromes other than the acquired immunodeficiency syndrome. Endoscopic sphincterotomy can provide symptomatic treatment for papillary stenosis in children with this condition, although the effect of sphincterotomy on the natural history of the sclerosing cholangitis is uncertain.

摘要

硬化性胆管炎是一种在儿童期很少发生的胆管树炎症性疾病,在患有获得性免疫缺陷综合征的成年人中已被认识到与乳头狭窄同时存在。一名10岁患有以T细胞功能缺陷以及免疫球蛋白A和G缺乏为特征的家族性免疫缺陷综合征的儿童,出现了乳头狭窄和与隐孢子虫肠炎相关的硬化性胆管炎。该患者表现出发热、黄疸、右上腹疼痛以及血清转氨酶和碱性磷酸酶浓度升高。内镜下括约肌切开术后疼痛和黄疸消退,但生化异常持续存在。该病例表明,乳头狭窄和硬化性胆管炎的组合在儿童和成人中均可发生,并且可能与获得性免疫缺陷综合征以外的免疫缺陷综合征相关。内镜下括约肌切开术可为患有这种疾病的儿童的乳头狭窄提供对症治疗,尽管括约肌切开术对硬化性胆管炎自然病程的影响尚不确定。

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