Manjima S, Naik Zameera, Keluskar Vaishali, Bagewadi Anjana
Department of Oral Medicine and Radiology, KLE VKIDS, Belgaum, Karnataka Belgaum, India.
Contemp Clin Dent. 2015 Mar;6(Suppl 1):S102-5. doi: 10.4103/0976-237X.152959.
Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies. Diagnosis is based on the major and minor clinical and radiographic criteria. Dentist plays a major role in the diagnosis of this disease due to the oral and maxillofacial manifestations of the syndrome. In some cases, jaw cysts are diagnosed by routine radiographs advised by the dentists. Odontogenic keratocysts in such syndromic patients will be multiple and extensive and in some cases results in cortical expansion and facial disfigurement. Thorough clinical examination and investigations prompt an early confirmation of the syndrome, which is very essential to avoid morbidity associated with the syndrome. Here, we report a case of multiple odontogenic cysts in a 16-year-old patient which later was diagnosed as a case of Gorlin Goltz syndrome.
戈林-戈尔茨综合征或基底细胞痣综合征是一种相对罕见的综合征,其特征为基底细胞痣、牙源性角化囊肿和骨骼异常。诊断基于主要和次要的临床及影像学标准。由于该综合征的口腔颌面部表现,牙医在这种疾病的诊断中起着主要作用。在某些情况下,牙医建议的常规X线片可诊断出颌骨囊肿。此类综合征患者的牙源性角化囊肿会多发且广泛,在某些情况下会导致皮质扩张和面部畸形。全面的临床检查和调查有助于早期确诊该综合征,这对于避免与该综合征相关的发病率非常重要。在此,我们报告一例16岁患者的多发性牙源性囊肿病例,该病例后来被诊断为戈林-戈尔茨综合征。