Palacios Enrique, Serou Michael, Restrepo Santiago, Rojas Rafael
Department of Radiology, Louisiana State University Health Sciences Center, New Orleans, LA 70131, USA.
Ear Nose Throat J. 2004 Jan;83(1):40-2.
We describe the imaging findings in a 13-year-old boy with nevoid basal cell carcinoma syndrome (NBCCS). The initial imaging work-up included plain radiographs and computed tomography (CT) of the facial area and mandible. CT detected large expansile cystic changes on both sides of the body and angle of the mandible. When the patient's condition worsened, magnetic resonance imaging (MRI) was performed to further characterize the nature of the lesions and to rule out intracranial anomalies. We agree with others who have published previous reports that although CT is valuable in elucidating osseous craniofacial anomalies associated with NBCCS, MRI is superior in demonstrating the internal composition and structure of the odontogenic keratocysts that are commonly seen in this syndrome.
我们描述了一名患有痣样基底细胞癌综合征(NBCCS)的13岁男孩的影像学表现。最初的影像学检查包括面部区域和下颌骨的X线平片及计算机断层扫描(CT)。CT检测到下颌骨体部和角部两侧有巨大的膨胀性囊性改变。当患者病情恶化时,进行了磁共振成像(MRI)以进一步明确病变的性质并排除颅内异常。我们赞同之前发表过报告的其他人的观点,即虽然CT在阐明与NBCCS相关的骨性颅面异常方面很有价值,但MRI在显示该综合征中常见的牙源性角化囊肿的内部成分和结构方面更具优势。