Bilateral ve tekrarlayan fasiyal paralizinin nadir nedeni: Melkersson-Rosenthal sendromu

Melkersson-Rosenthal Sendromu yineleyen periferik fasiyal paralizi, orofasiyal ödem ve fissürlü dil triadı ile karakterize granülomatöz hastalıktır. Bu yazımızda çocukluktan itibaren 2 kez sol ve bir kez sağ taraftan periferik paralizi atağı geçiren ve idiopatik fasiyal paralizi tanısı alan olgunın kliniğimize tekrar sağ tarafta periferik fasiyal paralizi ön tanısı ile yatırılıp tetkik ve takip sonucunda Melkersson-Rosenthal Sendromu (MRS) tanısı alan hastada; fasiyal paralizinin farklı tarafta ve farklı zamanlarda tekrarlayıcı olması ve tedaviye dirençli olması ve ayrıca gençlik çağında ender görülüyor olması nedeniyle sunulmuştur. Ancak bu sendromla ilgili gerek doğru etiyoloji ve gerekse sonuç veren tedavi açısından klinikopatolojik ek çalışmalara ihtiyaç duyulmaktadır.

A rare cause of bilateral and recurrent facial palsy: Melkersson-Rosenthal sendromu

Melkersson-Rosenthal syndrome is a granulomatous disease which is characterized by the triad of recurrent peripheral facial palsy, orofacial edema, and fssured tongue. In this article we presented one case who, since childhood, had had peripheral paralysis attack twice on the left side and once in the right side and was diagnosed with idiopathic paralysis before being admitted to our clinic for the second time with the preliminary diagnosis of peripheral facial paralysis on the right side and then diagnosed and followed up with the diagnosis of Melkers - son-Rosenthal Syndrome (MRS). We presented this case since the facial paralysis recurred on the different side and in different times and also since it remained resistant to treatment of steroids and it is seen rarely in adolescence. However, further clinic-pathological studies are required to investigate the etiology and fnd right treatment

___

  • 1. Zimmer WM, Rogers RS, Reeve CM, et al. Orofacial manifestations of Melkersson-Rosenthal syndrome. A study of 42 patients and review of 220 cases from the literature. Oral Surg Oral Med Oral Pathol 1992;74: 610-619.
  • 2. Ziem PE, Pfrommer C, Goerdt S, et al. Melkersson-Rosenthal syndrome in childhood: a challenge in differential diagnosis and treatment. Br J Dermatol 2000; 143:860-863.
  • 3. Armstrong DK, Burrows D. Orofacial granulomatosis. Int J Dermatol 1995;34:830-833.
  • 4. 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;54:404-413.
  • 5. Greene RM, Rogers RS. MRS: a review of 36 patients. J Am Acad Dermatol 1989;21:1263-1270.
  • 6. Cockerham KP, Hidayat AA, Cockerham GC, et al. Melkers - son-Rosenthal syndrome: new clinicopathologic fndings in 4 cases. Arch Ophthalmol 2000;118:227-232.
  • 7. Wong GA, Shear NH. Melkersson-Rosenthal syndrome as - sociated with allergic contact dermatitis from octyl and dodecyl gallates. Contact Dermatitis 2003;49:266-267.
  • 8. Camacho-Alonso F, Bermejo-Fenoll A, Lopez-Jornet P. Miescher’s cheilitis granulomatosa. A presentation of fve cases. Med Oral Patol Oral Cir Buccal 2004;9:427-429.
  • 9. Rogers RS 3rd. Melkersson-Rosenthal syndrome and orofacial granulomatosis. Dermatol Clin 1996;14:371-379.
  • 10. May M, Klein SR. Differrential diagnosis of facial nerve palsy. Otolaryngol Clin North Am 1991;24:613-645.
  • 11. Cockerham KP, Hidayat AA, Cockerham GC, et al. Melkersson-Rosenthal syndrome: new clinicopathologic fndings in 4 cases. Arch Ophthalmol 2000;118:227-232.
  • 12. Perez-Calderon R, Gonzalo-Garijo MA, Chaves A, et al. Cheilitis granulomatosa of Melkersson-Rosenthal syndrome: treatment with intralesional corticosteroid injections. Allergol Immunopathol 2004;32:36-38.
  • 13. Kruse-Losler B, Presser D, Metze D, et al. Surgical treatment of persistent macrocheilia in patients with Melkers - son-Rosenthal syndrome and cheilitis granulomatosa. Arch Dermatol 2005;141:1085-1091.
  • 14. Özdemir HH, Demir CF, M. Berilgen S, ve ark. Gebelik ve fasiyal dipleji: Nadir bir olgu. Dicle Med J 2012;39:419-421.
Dicle Tıp Dergisi-Cover
  • ISSN: 1300-2945
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 1963
  • Yayıncı: Cahfer GÜLOĞLU
Sayıdaki Diğer Makaleler

Clinical and laboratory characteristics of children with Kawasaki disease

FATİH AKIN, MELİKE EMİROĞLU, Ahmet SERT, ŞÜKRÜ ARSLAN, Ece Selma SOLAK

Assessment of ultrasound imaging and physical examination fndings in greater trochanteric pain syndrome

Fulya BAKILAN, Gökhan YÜCE, Ahmet BİCEN ÇAĞDAŞ, Kadir Serkan YALÇIN, Gökçe TANYERİ

Kaza ile üzerine cisim düşmesine bağlı hastaneye başvuran hastaların değerlendirilmesi

YAHYA TURAN, CEM UYSAL, Mustafa KORKMAZ, Tevfik YILMAZ, Cüneyt GOCMEZ, HÜSEYİN ÖZEVREN, Süleyman GÖREN, Adnan CEVİZ

Ailevi Akdeniz ateşi tanısı alan 186 olgunun klinik semptom ve MEFV geni mutasyonlarının incelenmesi

Mahmut ABUHANDAN, Cemil KAYA, AHMET GÜZELÇİÇEK

Aortokoroner bypass cerrahisi uygulanan olgularda EuroSCORE ve STS risk parametrelerinin karşılaştırılması

MEHMET SALİH AYDIN, Mustafa GÖZ, Abdussemet HAZAR, AYDEMİR KOÇARSLAN

Büyük trokanterik ağrı sendromunda ultrasonografi ve fizik muayene bulgularının değerlendirilmesi

Fulya BAKILAN, Gökhan YÜCE, Ahmet BİCEN, Kadir YALÇIN, Gökçe TANYERİ

Use of artifcial intelligence techniques for diagnosis of malignant pleural mesothelioma

ORHAN ER, A. Çetin TANRIKULU, Abdurrahman ABAKAY

The role of epidermal growth factor receptor in non-small cell lung cancer

AYŞE FEYDA NURSAL

Primer göz kapağı tümörlerinde histopatoloji sonuçları

Ali KURT, Sait Nafiz MUTLU, Halil İbrahim YENER, Nurettin BAYRAM, Sinan NAZLIM

CD79a, CD56 ve CD5 ko-ekspresyonu gösteren ve bifenotipik lösemi ile karışan AML M1'li çocuk olgu

Ayşen YILDIRIM TÜREDİ, Hüseyin GÜLEN