Chen Yong-Lin, He Deng-Qi, Yang Hai-Xia, Dou Yu
Department of Pathology, The First Hospital of Lanzhou University, Lanzhou 730000, Gansu Province, China.
Department of Oral Surgery, The First Hospital of Lanzhou University, Lanzhou 730000, Gansu Province, China.
World J Clin Cases. 2020 Nov 26;8(22):5611-5617. doi: 10.12998/wjcc.v8.i22.5611.
Schwannoma is a rare benign, encapsulated tumor of the nerve sheath under the tongue, mostly occurring as solitary tumors with classical histological pattern and several common morphological variants. To our knowledge, multiple schwannomas with pseudoglandular element synchronously occurring under the tongue are rare; we report herein the first such case.
A 53-year-old man had first noticed an isolated asymptomatic mass under the tongue, and as the mass grew, the tongue was elevated. Physical examination showed multiple oval neoplasms, and the overlying mucosa was normal. Computed tomography showed three low-density oval neoplasms under the tongue, which were cystic-solid with unclear boundary. The patient has no cutaneous tumors, VIII nerve tumors, or lens opacities and no history of neurofibromatosis 2 or confirmed schwannomatosis in any first-degree relative. Magnetic resonance imaging showed no evidence of vestibular schwannoma. The preoperative diagnosis was mucoepidermoid carcinoma. During hospitalization, all neoplasms were completely excised by surgeons through an intraoral approach under general anesthesia. The diagnosis of the multiple schwannomas with pseudoglandular element was made by histopathology after surgery. At the 15-mo follow-up visit, the patient had no sign of recurrence or development of other peripheral nerve tumors.
Although rare, multiple schwannomas with pseudoglandular element do exist in patients presenting with masses under the tongue. Oral surgeons should be aware of the existence of multiple schwannomas with pseudoglandular element when considering masses under the tongue due to the different prognosis between multiple schwannomas with pseudoglandular element and mucoepidermoid carcinoma.
神经鞘瘤是一种罕见的良性、有包膜的舌下神经鞘肿瘤,大多表现为具有典型组织学模式的孤立性肿瘤及几种常见的形态学变异型。据我们所知,舌下同时出现伴有假腺性成分的多发性神经鞘瘤很罕见;我们在此报告首例此类病例。
一名53岁男性最初注意到舌下有一个孤立的无症状肿块,随着肿块增大,舌体抬高。体格检查发现多个椭圆形肿物,其上覆盖黏膜正常。计算机断层扫描显示舌下有三个低密度椭圆形肿物,呈囊实性,边界不清。患者无皮肤肿瘤、Ⅷ神经肿瘤或晶状体混浊,且无神经纤维瘤病2型病史,任何一级亲属中也无确诊的神经鞘瘤病。磁共振成像未显示前庭神经鞘瘤的证据。术前诊断为黏液表皮样癌。住院期间,外科医生在全身麻醉下通过口内入路将所有肿物完整切除。术后经组织病理学诊断为伴有假腺性成分的多发性神经鞘瘤。在15个月的随访中,患者无复发迹象,也未出现其他周围神经肿瘤。
尽管罕见,但伴有假腺性成分的多发性神经鞘瘤确实存在于有舌下肿物的患者中。由于伴有假腺性成分的多发性神经鞘瘤与黏液表皮样癌的预后不同,口腔外科医生在考虑舌下肿物时应意识到伴有假腺性成分的多发性神经鞘瘤的存在。