McDougal P, Hill D J
Med J Aust. 1981 Jul 25;2(2):89-92. doi: 10.5694/j.1326-5377.1981.tb100806.x.
A review of the clinical and immunological features of 72 children with chronic arthritis revealed a similar pattern of disease in Australian children when compared with overseas studies. Most of the children had pauciarticular disease, but polyarthritis and systemic forms were seen. Although HLA=B27 was identified in some patients, no florid example of ankylosing spondylitis in childhood was seen. A small, but significant, number of children had evidence of potentially blinding iritis which developed insidiously, and one child had acute uveitis. Although elevated antistreptolysin-O titres and raised total IgM levels were seen in a significant number of children, they were not confined to any particular clinical pattern and were not of any major prognostic value. Half the children were severely incapacitated at the height of their disease, but follow-up for periods of up to five years revealed that fewer than 5% had a significant permanent disability.
一项对72名患慢性关节炎儿童的临床和免疫学特征的综述显示,与海外研究相比,澳大利亚儿童的疾病模式相似。大多数儿童患少关节型疾病,但也可见多关节炎和全身型。虽然在一些患者中发现了HLA-B27,但未见到童年期典型的强直性脊柱炎病例。一小部分但数量可观的儿童有潜在致盲性虹膜炎的证据,这种虹膜炎发展隐匿,还有一名儿童患急性葡萄膜炎。虽然相当数量的儿童抗链球菌溶血素O滴度升高和总IgM水平升高,但这些情况并不局限于任何特定的临床类型,也没有任何主要的预后价值。一半儿童在疾病高峰期严重致残,但长达五年的随访显示,不到5%的儿童有明显的永久性残疾。