Sherry D D, Kredich D W
Pediatrics. 1985 Oct;76(4):600-3.
Three children have been presented who have had long-standing, typical systemic juvenile rheumatoid arthritis. They also had a transient illness with thrombocytopenia, antiplatelet antibodies, and the simultaneous appearance of anti-DNA antibodies and hypocomplementemia. Other single abnormalities included the development of a positive ANA, Coombs, and lupus bands test. All responded to high-dose steroid therapy. Their similar clinical and serologic findings are noteworthy and represent one of the numerous complications seen in patients with systemic juvenile rheumatoid arthritis.
本文报告了3例患有长期典型全身型幼年类风湿关节炎的儿童。他们还曾患过一种短暂性疾病，伴有血小板减少、抗血小板抗体，同时出现抗DNA抗体和补体降低。其他单一异常包括抗核抗体、库姆斯试验和狼疮带试验呈阳性。所有患儿对大剂量类固醇治疗均有反应。他们相似的临床和血清学表现值得关注，代表了全身型幼年类风湿关节炎患者中众多并发症之一。
