Suga Kenichiro, Ogane Satoru, Muramatsu Kyotaro, Ohata Hitoshi, Uchiyama Takeshi, Takano Nobuo, Shibahara Takahiko, Eguchi Jun, Murakami Satoshi, Matsuzaka Kenichi
Department of Oral and Maxillofacial Surgery, Tokyo Dental College, Masago, Mihama-ku, Chiba, Japan.
Bull Tokyo Dent Coll. 2013;54(1):19-25. doi: 10.2209/tdcpublication.54.19.
Schwannomas (neurilemmomas) are benign neoplasms derived from Schwann cells of the neurilemma and appear most frequently on the auditory nerve or peripheral nerves of the skin. They arise in the oral and maxillofacial region infrequently, and very rarely in the center of the jaw. We herein present a case of a rare mandibular intraosseous schwannoma derived from the main trunk of the inferior alveolar nerve in a 33-year-old man. Fusiform expansion in the mandibular canal was observed and a mass showing the target sign in the mandibular canal was confirmed on T2-weighted and Gd contrastenhanced T1-weighted MRI. Based on these findings, an inferior alveolar nerve-derived schwannoma or other benign nervous system neoplasm was diagnosed. A buccal side cortical bone flap in the mandibular molar region was removed to expose the mass, which was then peeled away from the nerve fibers and completely removed. Some inferior alveolar nerve fibers that were connected to the mass were removed at the same time, but the remaining nerve fiber bundle was preserved. Histopathology confirmed the diagnosis of a schwannoma with Antoni type A and Antoni type B regions. Although the patient experienced extremely mild paresthesia in the skin over the mental region and mental foramen at immediately after surgery, this had almost entirely disappeared at 7 years and 4 months later, and there has been no tumor recurrence.
施万细胞瘤(神经鞘瘤)是源自神经鞘膜施万细胞的良性肿瘤,最常出现在听神经或皮肤的周围神经上。它们很少出现在口腔颌面部区域,极少出现在颌骨中央。我们在此报告一例罕见的下颌骨骨内施万细胞瘤,其起源于一名33岁男性的下牙槽神经主干。在T2加权和钆增强T1加权磁共振成像(MRI)上观察到下颌管呈梭形扩张,并证实下颌管内有一个呈靶征的肿块。基于这些发现,诊断为下牙槽神经源性施万细胞瘤或其他良性神经系统肿瘤。在下颌磨牙区切除颊侧皮质骨瓣以暴露肿块,然后将其从神经纤维上剥离并完全切除。同时切除了一些与肿块相连的下牙槽神经纤维,但保留了剩余的神经纤维束。组织病理学证实诊断为具有Antoni A型和Antoni B型区域的施万细胞瘤。尽管患者在术后即刻在颏部皮肤和颏孔处出现极轻微的感觉异常,但在7年4个月后几乎完全消失,且无肿瘤复发。