Infantile-onset multisystem inflammatory disease: a differential diagnosis of systemic juvenile rheumatoid arthritis
- PMID: 9108852
- DOI: 10.1016/s0022-3476(97)70238-5
Infantile-onset multisystem inflammatory disease: a differential diagnosis of systemic juvenile rheumatoid arthritis
Abstract
We describe four unrelated children with neonatal maculopapular rash, fever, arthritis, hepatosplenomegaly, lymphadenopathy, eye involvement, and neurologic symptoms. Radiographs of the joints were surprisingly similar, showing an abnormal epiphyseal and metaphyseal appearance. These clinical and radiologic findings allowed us to include these children in a very peculiar syndrome described as infantile-onset multisystemic inflammatory disease. A chondrosarcoma developed in one of our patients.
Comment in
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Recognition of infantile-onset multisystem inflammatory disease as a unique entity.J Pediatr. 1997 Apr;130(4):513-5. J Pediatr. 1997. PMID: 9108844 No abstract available.
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