M Jahad Nadia, Ridal Mohamed, Chafai Houda, Douida Amal, Naoual Hammas, Akamar Aamal, Maaroufi Mustapha, Alami Mohamed Nourredine El
Faculty of Medicine and Pharmacy, Sidi Mohammed Benabdellah University, Fez, Morocco.
Department of Otorhinolaryngology (ENT) and Head - Neck Surgery, Hassan II University Hospital, Fez, Morocco.
Pan Afr Med J. 2020 Jun 8;36:73. doi: 10.11604/pamj.2020.36.73.23500. eCollection 2020.
Schwannomas of the descending loop of the hypoglossal nerve are very rare. Existing literature of the schwannoma of the descending loop of the hypoglossal nerve is limited to two previously reported case. They are slow-growing tumors that may masquerade a carotid body tumor. We herein described a rare case of schwannoma of the descending loop of the hypoglossal nerve in the s right latero-cervical region with diagnostic imaging and histopathological findings. A 37-years-old woman has had a palpable firm, mobile mass in the right latero-cervical region, of imaging, MR images showed homogeneous hypointensity on T1-weighted imaging (T1-WI), heterogeneous hyperintensity on T2-WI, and heterogeneous enhancement on contrast-enhanced T1-WI. Diagnostic imaging using computed tomography (CT) and magnetic resonance imaging (MRI) was suspected of Chemodectoma or neurogenic tumor. At operation, a 4 cm mass arising from the descending loop of the hypoglossal nerve of was resected en bloc with the loop itself; Final diagnosis was confirmed on the basis of histopathological finding and intraoperative findings. Postoperative course was uneventful and the patient is free from disease recurrence at tree-year follow-up. En bloc resection remains the real curative treatment of Schwannomas, ensuring unlimited freedom from disease, although causing functional impairment which may be significant. Nonetheless recurrence should be prevented as, besides requiring reintervention, it may harbor a malignant evolution towards sarcoma. Schwannomas of the descending loop of the hypoglossal nerve may masquerade a chemodectoma of the carotid bifurcation and can be curatively resected without any functional impairment. This case confirmed the differential diagnosis on the basis of the intraoperative finding that the tumor was continuous with the hypoglossal nerve.
舌下神经降袢神经鞘瘤非常罕见。现有的关于舌下神经降袢神经鞘瘤的文献仅限于之前报道的两例病例。它们是生长缓慢的肿瘤,可能会伪装成颈动脉体瘤。我们在此描述了一例发生于右侧颈外侧区的舌下神经降袢神经鞘瘤的罕见病例,并给出了诊断性影像学和组织病理学结果。一名37岁女性在右侧颈外侧区可触及一个质地硬、可活动的肿块,影像学检查显示,磁共振成像(MR)图像在T1加权成像(T1-WI)上呈均匀低信号,在T2加权成像(T2-WI)上呈不均匀高信号,在对比增强T1-WI上呈不均匀强化。计算机断层扫描(CT)和磁共振成像(MRI)的诊断性影像学检查怀疑为化学感受器瘤或神经源性肿瘤。手术中,一个起源于舌下神经降袢的4厘米肿块与神经袢一并整块切除;最终诊断根据组织病理学检查结果和术中所见得以证实。术后病程平稳,患者在三年随访中无疾病复发。整块切除仍然是神经鞘瘤真正的根治性治疗方法,可确保无疾病复发,但可能会导致严重的功能障碍。尽管如此,仍应预防复发,因为除了需要再次干预外,复发可能会向肉瘤发生恶性演变。舌下神经降袢神经鞘瘤可能会伪装成颈动脉分叉处的化学感受器瘤,并且可以在不造成任何功能障碍的情况下进行根治性切除。该病例根据术中发现肿瘤与舌下神经相连这一结果证实了鉴别诊断。