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   A Rare Case of Gorlin-Goltz Syndrome Presented To the Emergency Department As Facial Swelling  
   
نویسنده Aloosi Suha N. ,Mahmood Kawa A. ,Ali Shakhawan M. ,Mahmud Payman Kh. ,Hasan Seerwan O. ,Muhamed Hawbash O.
منبع Frontiers In Emergency Medicine - 2018 - دوره : 2 - شماره : 4 - صفحه:1 -4
چکیده    Introduction: gorlin-goltz syndrome (ggs), also known as basal cell nevus syndrome, is a very rare autosomal dominant inherited disorder that is characterized by the development of numerous basal cell carcinoma. this article reports a case of ggs, emphasizing its clinical and radiographic manifestations. case presentation: we report here the case of a 35-year-old man who visited the maxillofacial emergency department due to left facial swelling. according to his clinical and radiographic examination we diagnosed him with ggs with no family history. the patient has multiple odontogenic keratocysts, rib anomalies, calcifications of the falx cerebri, lower jaw prognathism, frontal bossing, macrocephaly, and thick eyebrows. conclusion: a definitive diagnosis of ggs should be made by a multidisciplinary team including a maxillofacial surgeon and medical specialists. early diagnosis, treatment, and regular follow up are important to decrease complications, including oromaxillofacial deformation and destruction, and possible malignancy.
کلیدواژه Basal Cell Nevus Syndrome ,Case Reports ,Odontogenic Cysts ,Oral And Maxillofacial Surgeons
آدرس University Of Sulaimany, School Of Medicine, Faculty Of Dentistry, Department Of Oral And Maxillofacial Surgery, Iraq, University Of Sulaimany, School Of Medicine, Faculty Of Medicine, Department Of Radiology, Iraq, Sulaimany Teaching Hospital, Maxillofacial Department, Iraq, Sulaimany Teaching Hospital, Oral Medicine Department, ایران, Shahid Doctor Aso Neurosurgical And Ophthalmological Hospital, Surgical Emergency Hospital, Iraq, Sulaimany Teaching Hospital, Maxillofacial Department, Iraq
 
     
   
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