Avinash K R, Rajagopal K V, Ramakrishnaiah R H, Carnelio S, Mahmood N S
Department of Radiodiagnosis and Imaging, Kasturba Medical College, Manipal 576104, Karnataka, India.
Dentomaxillofac Radiol. 2007 Oct;36(7):434-6. doi: 10.1259/dmfr/54329867.
Osteochondroma of the mandibular condyle is fairly rare. We describe a case of this lesion in a 52-year-old woman who presented with symptoms of temporomandibular joint dysfunction. Although a panoramic radiograph demonstrated the bony exostosis, a pre-operative CT examination showed the relationship of the tumour to the condyle and also depicted soft-tissue changes secondary to the growth.
下颌骨髁突骨软骨瘤相当罕见。我们描述了一例发生在一名52岁女性身上的该病变病例,该患者表现出颞下颌关节功能障碍的症状。尽管全景X线片显示了骨外生骨疣,但术前CT检查显示了肿瘤与髁突的关系,还描绘了因肿瘤生长继发的软组织变化。