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一名全身型幼年特发性关节炎患者的肌肉磁共振成像异常。

Abnormal muscle MRI in a patient with systemic juvenile arthritis.

作者信息

Miller M L, Levinson L, Pachman L M, Poznanski A

机构信息

Department of Pediatrics, Northwestern University Medical School, Chicago, Illinois, USA.

出版信息

Pediatr Radiol. 1995 Nov;25 Suppl 1:S107-8.

PMID:8577498
Abstract

Although myositis has been described in children with systemic-onset juvenile arthritis (JA), its documentation by MRI has not been reported. We describe a 13-year-old boy with systemic-onset JA, severe myalgia, and elevated muscle enzymes, but normal muscle strength, who had an MRI consistent with myositis. Magnetic resonance imaging can identify the specific location of myositis, allowing more precise definition of a potential complication of systemic JA.

摘要

虽然在全身型幼年特发性关节炎(JA)患儿中已描述过肌炎,但尚未有通过MRI记录该病症的报道。我们描述了一名13岁患有全身型JA的男孩,他有严重肌痛和肌酶升高,但肌力正常,其MRI表现符合肌炎。磁共振成像能够识别肌炎的具体位置,从而更精确地界定全身型JA的一种潜在并发症。

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