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青少年慢性关节炎

Juvenile chronic arthritis.

作者信息

Ansell B M

机构信息

Division of Rheumatology, CRC, Northwick Park Hospital, Harrow, England.

出版信息

Scand J Rheumatol Suppl. 1987;66:47-50. doi: 10.3109/03009748709102521.

Abstract

Juvenile Chronic Arthritis is a relatively uncommon childhood disease. There are no absolute diagnostic tests and many classification criteria have evolved (4, 15, 7) based variably on joint number, disease course, associated clinical features and rheumatoid factor seropositivity. These are of no help diagnostically, but do allow investigative and follow-up studies to compare like with like. It is generally accepted that there are three main modes of onset, the commonest being pauci-articular with less than five joints in the first 3 to 6 months. Arising from the population immediately around the old MRC rheumatism unit at the Canadian Red Cross Memorial Hospital, Taplow, this accounted for 68%, with a poly-articular onset in 20% and systemic onset in 12%. Despite this low incidence of systemic illness, it remains a great challenge.

摘要

青少年慢性关节炎是一种相对罕见的儿童疾病。没有绝对的诊断测试,并且许多分类标准已经基于关节数量、病程、相关临床特征和类风湿因子血清阳性等因素而不断演变(4, 15, 7)。这些标准在诊断上并无帮助,但确实有助于进行调查和随访研究以进行同类比较。一般认为有三种主要的发病方式,最常见的是少关节型,在前3至6个月累及少于五个关节。该研究源于加拿大红十字会纪念医院(位于塔普洛)旧的医学研究委员会风湿病科周围的人群,其中少关节型发病占68%,多关节型发病占20%,全身型发病占12%。尽管全身型疾病的发病率较低,但它仍然是一个巨大的挑战。

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