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儿童期起病的赖特综合征,特别提及 HLA B27。病例报告及文献复习。

Reiter's disease with childhood onset having special reference to HLA B27. Report of a case and a review.

作者信息

Friis J

出版信息

Scand J Rheumatol. 1980;9(4):250-2. doi: 10.3109/03009748009112358.

Abstract

A case of Reiter's disease occurring in a girl aged 7 is reported. It commenced with diarrhoea precipitated by a salmonella infection. The patient has suffered from recurring arthritis accompanied by conjunctivitis, oral lesions and nail changes. The course was protracted, the patients having had two recurrences during a period of 6 1/2 years. The first of these lasted for more than one year, the second for a few months. The patient carries the histocompatibility antigen HLA B27 and a review of the literature would seem to establish that the correlation between Reiter's disease with childhood onset and this tissue antigen is as close as that reported in adults. It is stressed that the patient is now in complete remission and that no radiological changes have been demonstrated despite the protracted course. The patient shows no signs either of spondylitis or of sacro-iliitis.

摘要

报告了一例发生在7岁女孩身上的赖特综合征病例。该病始于沙门氏菌感染引发的腹泻。患者反复出现关节炎,并伴有结膜炎、口腔病变和指甲改变。病程迁延,患者在6年半的时间里复发了两次。第一次持续了一年多,第二次持续了几个月。患者携带组织相容性抗原HLA B27,文献综述似乎证实儿童期发病的赖特综合征与这种组织抗原之间的相关性与成人报道的一样密切。需要强调的是,患者目前已完全缓解,尽管病程迁延,但未发现放射学改变。患者也没有脊柱炎或骶髂关节炎的迹象。

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