Sarcoidosis is a multisystemic disorder of unknown cause characterized by non-caseating granulomas. The skin is affected in 20-35% of cases with systemic compromise (1), although exclusively cutaneous sarcoidosis has also been described (1). Diagnosis is frequently first established by a dermatologist. Cutaneous lesions have been well characterized, and commonly consist of papules, plaques (including angiolupoid and lupus pernio) and nodules; rarer forms include ulcerated, lichenoid, atrophic, psoriasiform, ichthyosiform, and vitiligo-like presentations (1). Oral mucosal lesions of sarcoidosis have been reported only rarely, and most descriptions come from the dental literature (2-5). However, clinical characterization of the lesions has not been properly performed in most of these publications: the lesions are imprecisely described as “masses”, “swellings”, “granulomas”, “gingivitis”, “gingival hyperplasia” or “gingival recession” (2-6). In none of these cases was any attempt made to correlate mucosal and cutaneous lesions. There are no studies comparing oral mucosal lesions of sarcoidosis with their cutaneous counterpart.
CITATION STYLE
Nico, M. M. S., Guimarães, A. L. M., Correa, P. Y. S. S., & Lourenço, S. V. (2016). Oral mucosal lesions in sarcoidosis: Comparison with cutaneous lesions. Acta Dermato-Venereologica, 96(3), 392–393. https://doi.org/10.2340/00015555-2262
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