Sixty-four consecutive patients with clinically or laboratory-supported definite multiple sclerosis (MS) were evaluated prospectively for evidence of primary Sjiigren's syndrome (SS). This diagnosis was established when a patient had objective keratoconjunctivitis sicca, xerostomia, or both together
Clinical and serologic study of sjögren's syndrome in patients with progressive systemic sclerosis
✍ Scribed by Thaddeus A. Osial JR.; Theresa L. Whiteside; Robert B. Buckingham; Gurmukh Singh; E. Leon Barnes; John M. Pierce; Gerald P. Rodnan
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 851 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0004-3591
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✦ Synopsis
Fifty-eight patients with progressive systemic sclerosis (PSS) were evaluated clinically and by biopsy of the minor salivary glands of the lips for the presence of Sjogren's syndrome. Clinical findings included dry eyes in 38%' dry mouth in 32%' parotid enlargement in 4%' and an abnormal Schirmer's test in 34%. Histologic changes in lip biopsies included lymphocytic infiltrates characteristic of Sjiigren's syndrome in 17 individuals (29%). In 19 (33%) there was periglandular and intraglandular fibrosis (PSS-fibrosis) without significant inflammation, an alteration characteristic of PSS per se. In the remaining 22 patients (38%) with PSS, no
📜 SIMILAR VOLUMES
## Abstract ## Objective. To address the clinical, serologic, pathologic, and immunogenetic features of sicca syndrome that occurs in systemic lupus erythematosus (SLE), as well as its similarities to, and differences from, sicca syndrome that occurs in primary Sjögren's syndrome (SS). ## Methods