喉旁间隙颈部交感链神经鞘瘤一例罕见病例及文献复习。

Alaa Senjab, Omar Al Ayoubi, Grace Tannous, Ahmad Al-Bitar, Arige Alassaf
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摘要

神经鞘瘤是一种罕见的良性肿瘤,起源于雪旺细胞。咽旁间隙肿瘤仅占所有头颈部肿瘤的0.5%左右,其中神经鞘瘤约占31%。其中,源自颈交感神经链(CSC)的神经鞘瘤特别罕见,但在临床上很重要。这些肿瘤生长缓慢,通常表现为模糊的症状,如轻度吞咽困难,从而延误诊断。成像技术,如计算机断层扫描(CT)和磁共振成像辅助评估。本文报告一例罕见的CSC神经鞘瘤病例,并回顾其他54例病例的诊断和临床特点。病例介绍:一名44岁阿拉伯女性,有轻度吞咽困难和右侧咽喉不适4个月的病史。体格检查显示沿右咽外侧壁有光滑、无压痛的粘膜下隆起。增强CT显示右侧椎旁间隙一边界清晰、均匀增强的肿块,取代颈动脉鞘,影像学表现与神经鞘瘤一致。经宫颈入路切除肿瘤,术中发现肿瘤起源于CSC。组织病理学证实为良性神经鞘瘤。术后,患者出现第一咬综合征(FBS),经保守治疗后症状逐渐改善。随访6个月,患者无症状,无复发迹象。结论:咽旁神经鞘瘤是一种罕见的神经源性肿瘤,常表现为症状模糊,诊断迟缓。CSC神经鞘瘤虽然不常见,但术后并发症如FBS和霍纳综合征的风险很高。准确的影像、早期识别和多学科规划是安全手术切除和最佳患者预后的必要条件。这个病例,连同我们的文献回顾,强调了肿瘤起源与临床行为和术后后遗症的相关性的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cervical Sympathetic Chain Schwannoma in the Parapharyngeal Space: A Rare Case and Literature Review.

Introduction: Schwannomas are rare, typically benign tumors arising from Schwann cells. Parapharyngeal space tumors account for only about 0.5% of all head and neck neoplasms, with schwannomas representing ~31% of these. Among these, schwannomas originating from the cervical sympathetic chain (CSC) are particularly rare but clinically important. These tumors grow slowly and often present with vague symptoms such as mild dysphagia, which delays diagnosis. Imaging techniques such as computed tomography (CT) and magnetic resonance imaging aid evaluation. This report presents a rare CSC schwannoma case and reviews 54 others to highlight diagnostic and clinical features.

Case presentation: A 44-year-old Arab female presented with a 4-month history of mild dysphagia and right-sided throat discomfort. Physical examination revealed a smooth, non-tender submucosal bulge along the right lateral pharyngeal wall. Contrast-enhanced CT demonstrated a well-circumscribed, homogeneously enhancing mass in the right paravertebral space, displacing the carotid sheath-radiologically consistent with a schwannoma. The tumor was excised via a transcervical approach and found intraoperatively to originate from the CSC. Histopathology confirmed a benign schwannoma. Postoperatively, the patient developed first-bite syndrome (FBS), managed conservatively with gradual symptom improvement. At 6-month follow-up, she remained asymptomatic with no evidence of recurrence.

Conclusion: Parapharyngeal schwannomas are rare neurogenic tumors that often present with vague symptoms, delaying diagnosis. CSC schwannomas, though uncommon, carry a high risk of postoperative complications such as FBS and Horner's syndrome. Accurate imaging, early recognition, and multidisciplinary planning are essential for safe surgical resection and optimal patient outcomes. This case, alongside our literature review, emphasizes the importance of correlating tumor origin with clinical behavior and postoperative sequelae.

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