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Rheumatology 2002; 41: 1190-1193
© 2002 British Society for Rheumatology

Paediatric Rheumatology

Sjögren syndrome: an unexpected disease occurring fourteen years after oligoarticular onset juvenile idiopathic arthritis

K. Bouayed, M.-A. Alyanakian1, C. Cordonnier2, S. Caillat-Zucman1, S. Testelin3, G. Lambrey4 and A.-M. Prieur

Unité d'Immunohématologie et Rhumatologie Pédiatriques, Hôpital des Enfants Malades, and
1 Service d'Immunologie Clinique, Hôpital Necker, Université Paris V, Paris
2 Service d'Anatomopathologie and
3 Service de Chirurgie Maxillo-Faciale et Stomatologie, CHU Amiens and
4 Service de Médecine Interne, Centre Hospitalier de Beauvais, Beauvais, France

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SIR, Sjögren syndrome (SS) is a very rare condition in childhood. Only single case reports or small groups of patients have been reported in the literature [1–4]. SS has been reported occasionally during the course of systemic lupus erythematosus or other connective tissue diseases in childhood, including a few cases of polyarticular-onset juvenile idiopathic arthritis (JIA), but never, to our knowledge, during the course of oligoarticular-onset JIA (OA-JIA). OA-JIA is the most frequent chronic inflammatory rheumatic condition in childhood, occurring mostly in girls before the age of 4 yr [5]. Chronic iridocyclitis is a frequent . . . [Full Text of this Article]


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