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Pulmonary fibrosis and myositis in a child with anti-Jo-1 antibody.

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.
AuthorsJ F Chmiel, H U Wessel, I N Targoff, L M Pachman
JournalThe Journal of rheumatology (J Rheumatol) Vol. 22 Issue 4 Pg. 762-5 (Apr 1995) ISSN: 0315-162X [Print] Canada
PMID7791178 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antibodies
  • Histidine-tRNA Ligase
Topics
  • Adolescent
  • Adult
  • Antibodies (analysis)
  • Child
  • Female
  • Histidine-tRNA Ligase (immunology)
  • Humans
  • Myositis (complications, immunology)
  • Pulmonary Fibrosis (complications, immunology)
  • Respiration Disorders (etiology)

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