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儿童新发系统性幼年特发性关节炎伴复发性心脏压塞。

Recurrent cardiac tamponade in a child with newly diagnosed systemic-onset juvenile idiopathic arthritis.

机构信息

Department of Pediatrics, Washington University School of Medicine, St Louis, MO, USA.

出版信息

J Clin Rheumatol. 2012 Sep;18(6):304-6. doi: 10.1097/RHU.0b013e3182685857.

Abstract

A previously healthy 5-year-old boy presented with prolonged fever, evanescent rash, and arthralgias. Diagnostic tests were significant for marked systemic inflammation. He rapidly developed pleural and pericardial effusions with cardiac tamponade, requiring placement of a pericardial drain. He briefly responded to nonsteroidal anti-inflammatory drugs and pulse methylprednisolone, but tamponade recurred shortly thereafter. Subsequently, he required high-dose intravenous immunoglobulin, infliximab, and anakinra. Thus, we report a patient with severe serositis and recurrent cardiac tamponade as the initial presentation of systemic juvenile idiopathic arthritis (sJIA) and review the literature regarding pericarditis and tamponade in sJIA. This potentially fatal complication of sJIA requires timely recognition and therapy to avoid significant morbidity and mortality.

摘要

一位原本健康的 5 岁男孩出现了长时间发热、一过性皮疹和关节痛。诊断性检查显示全身炎症明显。他迅速出现胸腔和心包积液并伴有心脏压塞,需要放置心包引流管。他曾短暂对非甾体抗炎药和脉冲甲基强的松龙有反应,但压塞随后再次发生。此后,他需要大剂量静脉注射免疫球蛋白、英夫利昔单抗和阿那白滞素。因此,我们报告了一例以严重浆膜炎和复发性心脏压塞为首发表现的全身型幼年特发性关节炎(sJIA)患者,并回顾了 sJIA 中有关心包炎和心脏压塞的文献。这种 sJIA 的潜在致命并发症需要及时识别和治疗,以避免严重的发病率和死亡率。

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