The clinical features of Sjögren's syndrome in Japanese children

49Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Sjögren's syndrome (SS) is thought to be uncommon in children. An epidemiological study to describe the clinical features distinguishing SS in Japanese children was performed by sending questionnaires to hospitals. A total of 61 cases of SS were reported from 1290 hospitals. The diagnosis of SS was based on histopathological changes and/or sialographic changes in the salivary glands. Forty-two cases had primary SS and 19 were secondary SS with other autoimmune disorders. Fourteen cases (65%) of secondary SS were associated with systemic lupus erythematosus. In primary SS, the initial symptoms were systemic manifestations (fever, exanthema, arthralgia, etc) except for sicca symptoms. In laboratory studies, antinuclear antibodies, elevated serum IgG, rheumatoid factor, anti-Ro/SS-A antibodies and anti-La/SS-B antibodies were frequently observed. 1997 Japan Pediatric Society.

Author supplied keywords

Cite

CITATION STYLE

APA

Tomiita, M., Saito, K., Kohno, Y., Shimojo, N., Fujikawa, S., & Niimi, H. (1997). The clinical features of Sjögren’s syndrome in Japanese children. Pediatrics International, 39(2), 268–272. https://doi.org/10.1111/j.1442-200X.1997.tb03597.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free