Sobjanek M, Żelazny I, Włodarkiewicz A, Nowicki R, Michajłowski I. Case reportMelkersson-Rosenthal syndrome. Case report and review of the literature. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii. 2008;25(1):43-47.
APA
Sobjanek, M., Żelazny, I., Włodarkiewicz, A., Nowicki, R., & Michajłowski, I. (2008). Case reportMelkersson-Rosenthal syndrome. Case report and review of the literature. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, 25(1), 43-47.
Chicago
Sobjanek, Michał, Izabela Żelazny, Adam Włodarkiewicz, Roman Nowicki, and Igor Michajłowski. 2008. "Case reportMelkersson-Rosenthal syndrome. Case report and review of the literature". Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii 25 (1): 43-47.
Harvard
Sobjanek, M., Żelazny, I., Włodarkiewicz, A., Nowicki, R., and Michajłowski, I. (2008). Case reportMelkersson-Rosenthal syndrome. Case report and review of the literature. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, 25(1), pp.43-47.
MLA
Sobjanek, Michał et al. "Case reportMelkersson-Rosenthal syndrome. Case report and review of the literature." Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, vol. 25, no. 1, 2008, pp. 43-47.
Vancouver
Sobjanek M, Żelazny I, Włodarkiewicz A, Nowicki R, Michajłowski I. Case reportMelkersson-Rosenthal syndrome. Case report and review of the literature. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii. 2008;25(1):43-47.
Melkersson-Rosenthal syndrome is characterized by a triad of signs: oedema of the face and lips, recurrent peripheral facial nerve paralysis, and fissured tongue (lingua plicata). Monosymptomatic or oligosymptomatic forms of Melkersson-Rosenthal syndrome are common. Aetiology is still unclear. Genetic, autoimmune and infectious factors have been proposed. The authors present a case of a 40-year-old man with Melkersson-Rosenthal syndrome treated with good effect by combination therapy consisting of intralesional injection of triamcinolone, and oral dapsone. The authors also review the literature of clinical presentation and current treatment of this rare syndrome.