Rais Mohammed Amir, Naouri Yahia, Awad Ahmed K
Faculty of Medicine of Algiers, University of Algiers, Algiers 16000, Algeria.
Mustapha Pacha University Hospital, Algiers 16014, Algeria.
J Surg Case Rep. 2023 Jan 17;2023(1):rjac578. doi: 10.1093/jscr/rjac578. eCollection 2023 Jan.
Schwannoma, also called neurilemmoma, is a rare neurogenic tumor exclusively benign that develops from a variety of glial nerve cells called Schwann cells. We present a 26-year-old female patient who was admitted with a history of dysphagia, headache and swelling going from the lower limit of the ear to the floor of the neck on the left side, which has been slowly progressing for 5 years. Upon local clinical examination, a well-defined mass was revealed, 6 × 5 cm in size, non-painful spontaneously, painful on direct palpation of the left neck. Computed tomography scan has shown a well-circumscribed large mass with heterogenous areas of enhancement in the left parapharyngeal space displacing the submandibular gland superiorly and the carotid sheath anterolaterally and compressing the oropharyngeal airway. Excision of the tumor was done by a combined route without post-operative complications noted. Histopathological examination revealed a benign schwannoma without the identification of the nerve of origin.
施万细胞瘤,也称为神经鞘瘤,是一种罕见的仅为良性的神经源性肿瘤,由一种称为施万细胞的多种神经胶质细胞发展而来。我们报告一名26岁女性患者,因吞咽困难、头痛以及左侧从耳垂下方至颈部底部的肿胀病史入院,该症状已缓慢进展5年。经局部临床检查,发现一个边界清晰的肿块,大小为6×5厘米,自发无疼痛,直接触诊左侧颈部时有疼痛。计算机断层扫描显示在左咽旁间隙有一个边界清楚的大肿块,有不均匀强化区域,使下颌下腺向上移位,颈动脉鞘向前外侧移位,并压迫口咽气道。通过联合路径切除肿瘤,未发现术后并发症。组织病理学检查显示为良性施万细胞瘤,未识别出起源神经。