Sawada Kunihiko, Schulze Dirk, Matsumoto Kunihito, Hirai Shigenori, Hashimoto Koji, Honda Kazuya
Department of Oral and Maxillofacial Radiology, Nihon University School of Dentistry.
J Oral Sci. 2015;57(4):389-92. doi: 10.2334/josnusd.57.389.
We describe a rare case of osteochondroma of the coronoid process of mandible accompanied by severe trismus in a 14-year-old Japanese boy. The patient had initially been diagnosed as having internal derangement of the temporomandibular joint (TMJ), and conservative treatment had failed to improve the symptoms. Despite extremely limited TMJ movement, panoramic radiography revealed no abnormality, but magnetic resonance imaging suggested internal derangement of the left TMJ. Five months later, the trismus worsened and computed tomography revealed a bone-like mass confluent with the coronoid process, which was finally diagnosed as osteochondroma. The patient then underwent intra-oral coronoidectomy.
我们描述了一例罕见的下颌骨冠状突骨软骨瘤病例,该病例发生在一名14岁的日本男孩身上,并伴有严重的牙关紧闭。患者最初被诊断为颞下颌关节(TMJ)内紊乱,保守治疗未能改善症状。尽管TMJ活动极度受限,但全景X线片未显示异常,而磁共振成像提示左侧TMJ内紊乱。五个月后,牙关紧闭加重,计算机断层扫描显示一个与冠状突相连的骨样肿块,最终被诊断为骨软骨瘤。该患者随后接受了口内冠状突切除术。