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Pulmonary fibrosis and myositis in a child with anti-Jo-1 antibody
J F Chmiel1, H U Wessel, I N Targoff
1Department of Pediatrics, Northwestern University Medical School, Chicago, IL, USA.
Insights
This report details the first child diagnosed with anti-Jo-1 antibody syndrome, presenting with progressive lung disease and inflammatory myositis. Early diagnosis and management are crucial for this rare autoimmune condition in pediatric cases.
Area of Science:
- Pediatric Rheumatology
- Pulmonology
- Autoimmune Diseases
Background:
- Anti-Jo-1 antibodies are associated with idiopathic inflammatory myopathies and interstitial lung disease.
- Pediatric cases of anti-Jo-1 antibody-positive disease are exceptionally rare, with limited documented evidence.
Abstract:
This is the first report of a child with anti-Jo-1 antibody. At 10, she had a chronic cough, wheezing, dyspnea on exertion, a combined obstructive and restrictive ventilatory defect, and a decreased diffusion capacity compatible with alveolar fibrosis (lung biopsy). By age 12, she developed arthralgias, malar rash, frontal alopecia, Raynaud's phenomenon, and was seropositive for antinuclear antibodies, (SSA)Ro, Jo-1 and rheumatoid factor. At 16, symptomatic inflammatory myositis (elevated creatinine kinase, muscle biopsy) was documented with persistent anti-Jo-1. Her pulmonary symptoms have progressed despite appropriate therapy. Although her digits have become sausage shaped with swan neck deformities, joint pain is not frequent.
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