| Literature DB >> 17643198 |
M Gwosdz1, A Körber, U Hillen, J Dissemond.
Abstract
Sjögren syndrome is a rare chronic systemic autoimmune disease characterized by progressive dryness of the mucous membranes. There are many variable clinical manifestations. A 40-year-old woman presented with painful leg ulcers refractory to various therapies. She had a history of xerostomia and xerophthalmia for several years. Based on clinical, serologic and histopathologic findings, we diagnosed leg ulcers in primary Sjögren syndrome. Combing immunosuppressive therapy with phase-adapted modern wound-therapy resulted in a complete healing of the ulcers. In the case of clinically atypical leg ulcers, Sjögren syndrome should be considered as a rare differential diagnostic possibility.Entities:
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Year: 2008 PMID: 17643198 DOI: 10.1007/s00105-007-1375-0
Source DB: PubMed Journal: Hautarzt ISSN: 0017-8470 Impact factor: 0.751