How is Sjögren’s Syndrome Related to Scleroderma?
Over 20 percent of patients with systemic sclerosis and a few with localized scleroderma also have secondary Sjögren’s Syndrome. It is more often detected in persons with the limited form of systemic sclerosis. The symptoms and examination findings and methods of diagnosis and treatment in Sjögren’s Syndrome secondary to scleroderma are identical to those in primary Sjögren’s Syndrome. Special problems encountered by scleroderma patients are reduced mouth opening, finger-tip ulcers, and deformities of the fingers, all of which interfere with maintaining good oral hygiene. Therefore it is particularly important for scleroderma patients to consult their dentists and periodontists to make sure that they use appropriate prophylactic measures. Editor’s Note: This article was printed in the form of a brochure available in our store on our Web site or via download. The information provided is for educational purposes only. Any drugs or treatments mentioned should be discussed with your own ph
