| Literature DB >> 20237928 |
Tomomi Aizawa-Yashiro1, Eishin Oki, Kazushi Tsuruga, Tohru Nakahata, Etsuro Ito, Hiroshi Tanaka.
Abstract
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.Entities:
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Year: 2010 PMID: 20237928 DOI: 10.1007/s00296-010-1413-6
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631