TY  - JOUR
T1  - Bilateral ve tekrarlayan fasiyal paralizinin nadir nedeni: Melkersson-Rosenthal sendromu
AU  - Akdağ, Mehmet
AU  - Özkurt, Fazıl
AU  - Yılmaz, Beyhan
AU  - Topçu, İsmail
AU  - Meriç, Faruk
PY  - 2015
DA  - May
DO  - 10.5798/diclemedj.0921.2015.01.0541
JF  - Dicle Medical Journal
JO  - diclemedj
PB  - Dicle University
WT  - DergiPark
SN  - 1300-2945
SP  - 102
EP  - 106
VL  - 42
IS  - 1
LA  - tr
AB  - 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. Anahtar kelimeler: Melkersson-rosenthal sendromu, fasiyal paralizi, fissürlü dil
KW  - Melkersson-rosenthal sendromu
KW  - fasiyal paralizi
KW  - fissürlü dil
N2  - Melkersson-Rosenthal syndrome is a granulomatous disease which is characterized by the triad of recurrent peripheral facial palsy, orofacial edema, and fissured 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 Melkersson-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 find right treatment procedures for this syndrome
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UR  - https://doi.org/10.5798/diclemedj.0921.2015.01.0541
L1  - https://dergipark.org.tr/en/download/article-file/54543
ER  -