Melkersson-Rosenthal syndrome (MRS) is a rare neuromucocutaneous syndrome characterized by recurrent facial paralysis, orofacial edema and fissured tongue. Oligosymptomatic and monosymptomatic forms are more common than the triad. The presence of two manifestations or one manifestation with granulomatous cheilitis in biopsy is sufficient to make diagnosis of Melkersson-Rosenthal syndrome. We present a 12 years-old male who is diagnosed Melkersson-Rosenthal syndrome.
Melkersson E. Case of recurrent facial paralysis with angioneurotic edema. Hygiea. 1928;90:737-41.
Rosenthal C. Klinisch-erbbiologischer Beitrag zur Konstitutions-pathologie: Gemeinsames Auftreten von (rezidivierender familiärer). Facialislähmung, angioneurotischem gesichtsödem und lingua plicata in arthritismus-familien. Ztschr Neurol Psychiatry. 1931;131:475-501.
Hornstein OP. Melkersson–Rosenthal syndrome: A neuro-mucocutaneous disease of complex origin. Curr Probl Derm. 1973;5:117–56.
Zimmer WM, Rogers RS, Reeve CM, Sheridan PJ. Orofacial manifestations of Melkersson-Rosenthal syndrome:a study of 42 patients and review of 220 cases from literature. Oral Surg Oral Med Oral Pathol. 1992;74:610-9.
McGrath DS, Doyle C, Bredin CP. MelkerssonRosenthal syndrome-a differential diagnosis of facial sarcoidosis. Ir J Med Sci. 1997;166:253-6.
Morales C, Penarrocha M, Bagan JV, et al. Immunological study of MRS. Lack of response to food additive challenge. Clin Exp Allergy. 1995;25:260-4.
Armstrong DK, Burrows D. Orofacial granulomatosis. Int J Dermatol. 1995;34:830-3.
Worsaae N, Christensen KC, Schiodt M, et al. MRS and cheilitis granulomatosa. A clinicopathological study of thirty three patients with special reference to their oral lesions. Oral Surg Oral Med Oral Pathol. 1982;54:404-13.
Greene RM, Rogers RS. MRS: a review of 36 patients. J Am Acad Dermatol. 1989;21:1263-70.
Rawlings NG, Valenzuela AA, Allen LH, Heathcote JG. Isolated eyelid edema in Melkersson–Rosenthal syndrome: a case series. Eye. 2012;26:163-6.
Cockerham KL, Hidayat AA, Cockerham CG. Melkersson Rosenthal Syndrome. New Clinicopathologic Findings in 4 Cases. Arch Opthalmol. 2000;118:227-32.
Vistnes LM, Kernahan DA. The Melkersson– Rosenthal syndrome. Plast Reconstr Surg. 1971;48:126–32. van der Waal RI, Schulten EA, van der Meij EH, van de Scheur MR, Starink TM, van der Waal I. Cheilitis granulomatosa: overview of 13 patients with longterm follow-up results of management. Int J Dermatol. 2002;41:225-9.
Şafak MA, Göçmen H, Kılıç R. Melkersson Rosenthal Sendromu: Üç Olgu Sunumu. Otoskop 2001;2:78-81.
Elias MK, Mateen FJ, Weiler CR. The Melkersson– Rosenthal syndrome: a retrospective study of biopsied cases. J Neurol. 2013;260:138–43.
Saltık S, Karatoprak EY, Çetin AF. Yineleyen fasiyal sinir paralizisinin ender bir nedeni: Melkersson Rosenthal sendromu. Göztepe Tıp Dergisi. 2012;27:193-6.
Melek H, Köken R, Bükülmez A. et al. MelkerssonRosenthal Sendromu: Bir Olgu Sunumu. Güncel Pediatri. 2007;5:82-4.
Dodi I, Verri R, Brevi B, et al. Monosymptomatic Melkersson-Rosenthal syndrome in an 8-year old boy. Acta Biomed. 2006;77:20-3.
Ziem PE, Pfrommer C, Goerdt S, Orfanos CE, Blume-Peytavi U. Melkersson-Rosenthal syndrome in childhood: a challenge in differential diagnosis and treatment. Br J Dermatol. 2000;143:860-3.
Litvyakova LI, Bellanti JA.Orofacial Edema: A Diagnostic And Therapeutic Challenge For the Clinician. Ann Allergy Asthma Immunol. 2000;84:188
Tekrarlayan Fasiyal Paralizili bir olgu: Melkersson-Rosenthal Sendromu
Melkersson-Rosenthal sendromu (MRS), tekrarlayan fasiyal paralizi, orofasiyal ödem, dilde fissürle karakterize nadir bir nöromukokütanöz sendromdur. Oligosemptomatik ve monosemptomatik olgular, klasik triaddan sık görülür. Bulguların ikisinin görülmesi veya bulguların biri ve biyopside granülomatöz keilitin varlığı Melkersson-Rosenthal sendromu tanısı için yeterlidir. Bu yazıda Melkersson-Rosenthal sendromu tanısı alan 12 yaşında bir erkek sunulmuştur.
Melkersson E. Case of recurrent facial paralysis with angioneurotic edema. Hygiea. 1928;90:737-41.
Rosenthal C. Klinisch-erbbiologischer Beitrag zur Konstitutions-pathologie: Gemeinsames Auftreten von (rezidivierender familiärer). Facialislähmung, angioneurotischem gesichtsödem und lingua plicata in arthritismus-familien. Ztschr Neurol Psychiatry. 1931;131:475-501.
Hornstein OP. Melkersson–Rosenthal syndrome: A neuro-mucocutaneous disease of complex origin. Curr Probl Derm. 1973;5:117–56.
Zimmer WM, Rogers RS, Reeve CM, Sheridan PJ. Orofacial manifestations of Melkersson-Rosenthal syndrome:a study of 42 patients and review of 220 cases from literature. Oral Surg Oral Med Oral Pathol. 1992;74:610-9.
McGrath DS, Doyle C, Bredin CP. MelkerssonRosenthal syndrome-a differential diagnosis of facial sarcoidosis. Ir J Med Sci. 1997;166:253-6.
Morales C, Penarrocha M, Bagan JV, et al. Immunological study of MRS. Lack of response to food additive challenge. Clin Exp Allergy. 1995;25:260-4.
Armstrong DK, Burrows D. Orofacial granulomatosis. Int J Dermatol. 1995;34:830-3.
Worsaae N, Christensen KC, Schiodt M, et al. MRS and cheilitis granulomatosa. A clinicopathological study of thirty three patients with special reference to their oral lesions. Oral Surg Oral Med Oral Pathol. 1982;54:404-13.
Greene RM, Rogers RS. MRS: a review of 36 patients. J Am Acad Dermatol. 1989;21:1263-70.
Rawlings NG, Valenzuela AA, Allen LH, Heathcote JG. Isolated eyelid edema in Melkersson–Rosenthal syndrome: a case series. Eye. 2012;26:163-6.
Cockerham KL, Hidayat AA, Cockerham CG. Melkersson Rosenthal Syndrome. New Clinicopathologic Findings in 4 Cases. Arch Opthalmol. 2000;118:227-32.
Vistnes LM, Kernahan DA. The Melkersson– Rosenthal syndrome. Plast Reconstr Surg. 1971;48:126–32. van der Waal RI, Schulten EA, van der Meij EH, van de Scheur MR, Starink TM, van der Waal I. Cheilitis granulomatosa: overview of 13 patients with longterm follow-up results of management. Int J Dermatol. 2002;41:225-9.
Şafak MA, Göçmen H, Kılıç R. Melkersson Rosenthal Sendromu: Üç Olgu Sunumu. Otoskop 2001;2:78-81.
Elias MK, Mateen FJ, Weiler CR. The Melkersson– Rosenthal syndrome: a retrospective study of biopsied cases. J Neurol. 2013;260:138–43.
Saltık S, Karatoprak EY, Çetin AF. Yineleyen fasiyal sinir paralizisinin ender bir nedeni: Melkersson Rosenthal sendromu. Göztepe Tıp Dergisi. 2012;27:193-6.
Melek H, Köken R, Bükülmez A. et al. MelkerssonRosenthal Sendromu: Bir Olgu Sunumu. Güncel Pediatri. 2007;5:82-4.
Dodi I, Verri R, Brevi B, et al. Monosymptomatic Melkersson-Rosenthal syndrome in an 8-year old boy. Acta Biomed. 2006;77:20-3.
Ziem PE, Pfrommer C, Goerdt S, Orfanos CE, Blume-Peytavi U. Melkersson-Rosenthal syndrome in childhood: a challenge in differential diagnosis and treatment. Br J Dermatol. 2000;143:860-3.
Litvyakova LI, Bellanti JA.Orofacial Edema: A Diagnostic And Therapeutic Challenge For the Clinician. Ann Allergy Asthma Immunol. 2000;84:188