Department of Pediatrics, Hirosaki University School of Medicine, Hirosaki 036-8562, Japan.
Rheumatol Int. 2012 May;32(5):1359-61. doi: 10.1007/s00296-010-1413-6. Epub 2010 Mar 18.
A 7-year-old Japanese boy with a 4-month history of systemic juvenile idiopathic arthritis (s-JIA) experienced disease flare with spiking fever, exanthema and arthralgia. He then developed progressive dyspnea due to severe pericarditis, and proinflammatory hypercytokinemia was suspected. Methylprednisolone pulse therapy was ineffective and echocardiography showed massive pericardial effusion had persisted. Alternatively, subsequent intravenous immunoglobulin (IVIG) therapy resulted in dramatic resolution of the pericardial effusion, and his general condition significantly improved within a few days. This case report may lend further support the use of IVIG for selected patients with s-JIA and severe pericarditis.
一名 7 岁日本男孩,患有系统性幼年特发性关节炎(s-JIA)4 个月,出现发热、皮疹和关节痛等疾病发作。随后,由于严重的心包炎,他出现进行性呼吸困难,怀疑存在促炎细胞因子血症。甲泼尼龙脉冲治疗无效,超声心动图显示大量心包积液持续存在。随后,静脉注射免疫球蛋白(IVIG)治疗导致心包积液明显消退,几天后他的一般状况显著改善。本病例报告可能进一步支持 IVIG 用于 s-JIA 合并严重心包炎的特定患者。