Aust Dent J. 2014 Mar;59(1):121-4. doi: 10.1111/adj.12137.
Gorlin and Goltz described a syndrome in which multiple basal cell carcinomas, odontogenic keratocysts and bifid ribs occurred in combination. The jaw keratocysts are a consistent feature of 'Gorlin-Goltz' or naevoid basal cell carcinoma syndrome. Central nervous system and ocular involvement occurred together with the fairly typical facial features of frontal bossing and hypertelorism. This case report documents the pathology associated with an impacted maxillary canine tooth in a boy with Gorlin-Goltz syndrome. The patient presented for investigation of the failure of eruption of the right permanent maxillary canine tooth. Radiographic investigation showed the presence of a well circumscribed radiolucency located around the crown of an impacted right maxillary canine tooth. The patient's medical history revealed a medulloblastoma that was treated 13 years ago. The right maxillary canine tooth and associated peri-coronal tissue were removed under general anaesthetic. A diagnosis of a keratocystic odontogenic tumour with an associated adenomatoid odontogenic tumour was made. The common differential diagnoses for a peri-coronal radiolucency in the maxilla that need to be considered by dentists include a dentigerous cyst, follicular keratocystic odontogenic tumour and adenomatoid odontogenic tumour. A rare case of both keratocystic odontogenic tumour and associated follicular adenomatoid odontogenic tumour is described in a patient with naevoid basal cell carcinoma syndrome.
戈林-戈尔茨综合征(Gorlin-Goltz syndrome)是一种常染色体显性遗传疾病,其特征为多发性基底细胞癌、牙源性角化囊肿和分叉肋骨。下颌骨角化囊肿是“戈林-戈尔茨综合征”或痣样基底细胞癌综合征的一个特征。中枢神经系统和眼部受累常与额骨突出和眼距过宽等相当典型的面部特征同时发生。本病例报告记录了一名患有戈林-戈尔茨综合征的男孩的上颌尖牙阻生所伴有的病理学改变。该患者因右上颌恒尖牙萌出失败就诊。影像学检查显示,一颗已萌出的右上颌尖牙的牙冠周围有一个边界清楚的透光区。患者的病史显示,他在 13 年前曾接受过髓母细胞瘤治疗。在全身麻醉下,右上颌尖牙及其周围的牙周组织被切除。诊断为角化囊肿性牙源性肿瘤伴腺瘤样牙源性肿瘤。牙医需要考虑的上颌牙冠周围透光区的常见鉴别诊断包括含牙囊肿、滤泡型角化囊肿性牙源性肿瘤和腺瘤样牙源性肿瘤。本文报道了一例罕见的戈林-戈尔茨综合征患者,同时患有角化囊肿性牙源性肿瘤和相关的滤泡状腺瘤样牙源性肿瘤。