Kamath Panduranga M, Dosemane Deviprasad, Sreedharan Suja S, Majeed Nazeem A, Shenoy Vijendra S
Professor, Department of ENT, Kasturba Medical College , Mangalore, Manipal University, India .
Associate Professor, Department of ENT, Kasturba Medical College , Mangalore, Manipal University, India .
J Clin Diagn Res. 2016 Apr;10(4):MD03-4. doi: 10.7860/JCDR/2016/16391.7588. Epub 2016 Apr 1.
Among the parapharyngeal tumours, salivary gland tumours are the commonest, followed by schwannomas, which are slow growing benign tumours. Half of the parapharyngeal schwannomas originate from the vagus. Complete surgical excision is the treatment of choice. We hereby present two cases of parapharyngeal schwannomas, one which had presented as an intraoral mass and the other as a swelling in the neck. The first case, a 57-year-old female patient complained of a slowly increasing swelling in the left side of the throat since 3 months, associated with pain and dysphagia. In the Contrast Enhanced CT scan of the neck, a well-defined cystic lesion with central enhancing solid components (4cm X 4.5cm X 3cm) was seen in the left parapharyngeal region. The second case, a 39-year-old male patient complained of a painless, gradually increasing swelling below the lobule of the right ear since one month. Examination revealed a solitary, nontender, firm and mobile swelling of 2cm X 2cm below the lobule of the right ear. In Contrast Enhanced CT scan of the neck, an enhancing lesion was seen involving the right parapharyngeal space, post-styloid compartment. Both the patients underwent trans-cervical surgical excision. Vagal nerve schwannoma is rare. The majority of the cases present with a slow growing neck swelling without neurological deficit. Complete surgical excision of the tumour is important to prevent recurrence.
在咽旁肿瘤中,涎腺肿瘤最为常见,其次是神经鞘瘤,这是一种生长缓慢的良性肿瘤。半数咽旁神经鞘瘤起源于迷走神经。完整手术切除是首选治疗方法。我们在此报告两例咽旁神经鞘瘤病例,一例表现为口内肿物,另一例表现为颈部肿物。第一例,一名57岁女性患者自3个月前起左侧咽部出现逐渐增大的肿物,伴有疼痛和吞咽困难。颈部增强CT扫描显示,左侧咽旁区域可见一个边界清晰的囊性病变,中央有强化的实性成分(4cm×4.5cm×3cm)。第二例,一名39岁男性患者自1个月前起右耳垂下方出现无痛性、逐渐增大的肿物。检查发现右耳垂下方有一个2cm×2cm的孤立、无压痛、质地硬且可活动的肿物。颈部增强CT扫描显示,右侧咽旁间隙茎突后区有一个强化病变。两名患者均接受了经颈部手术切除。迷走神经鞘瘤罕见。大多数病例表现为颈部肿物生长缓慢且无神经功能缺损。完整手术切除肿瘤对于预防复发很重要。