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一例不寻常且表现不一致的颅底副神经节瘤

An Unusual and Discrepant Presentation of a Skull Base Paraganglioma.

作者信息

Patel Raj, Allam Yusuf A, Shukairy Mohammad K, Kircher Matthew

机构信息

Otolaryngology, Loyola University Medical Center, Maywood, USA.

Anatomical Sciences, University of Michigan, Ann Arbor, USA.

出版信息

Cureus. 2024 Aug 7;16(8):e66394. doi: 10.7759/cureus.66394. eCollection 2024 Aug.

Abstract

Paragangliomas are rare tumors of neuroendocrine origin. Within the head and neck, these tumors are slow-growing and locally destructive, with a small malignant potential. Vagal paragangliomas (VPs) originate from paraganglia around the vagus nerve, typically at the level of the skull base. Cranial nerve deficits are common at presentation, with the vagus nerve and hypoglossal nerves being most affected. Similarly, hypoglossal paragangliomas (HPs) originate from around the hypoglossal nerve but are extremely rare and less documented. We describe the case of a patient presenting with an isolated hypoglossal nerve palsy in the setting of a tumor that radiologically represents a VP. A descriptive literature review was conducted to highlight presentation, management, and outcomes related to this pathology. A 65-year-old male presented to the clinic with tongue fasciculations and several years of dysarthria. Physical examination showed intermittent right tongue fasciculations in addition to ipsilateral hemi-atrophy. A computed tomography scan with contrast revealed an enhancing skull base mass inferior to the right carotid space. Subsequently, magnetic resonance imaging with contrast further delineated its anatomic involvement and site of origin, allowing for the diagnosis of a VP. After further discussion with the patient about his clinical findings, the decision was made to proceed with observation and serial imaging. Skull base paragangliomas are a rare pathologic entity that may pose a challenging multidisciplinary approach to optimize management strategies. Treatment may vary on a case-by-case basis and is dependent on patient and tumor characteristics.

摘要

副神经节瘤是一种罕见的神经内分泌起源的肿瘤。在头颈部,这些肿瘤生长缓慢且具有局部破坏性,恶变潜能较小。迷走神经副神经节瘤(VPs)起源于迷走神经周围的副神经节,通常位于颅底水平。就诊时颅神经功能缺损很常见,其中迷走神经和舌下神经受影响最为严重。同样,舌下神经副神经节瘤(HPs)起源于舌下神经周围,但极为罕见且文献记载较少。我们描述了一例患者,在影像学表现为VPs的肿瘤背景下出现孤立性舌下神经麻痹。进行了描述性文献综述,以突出与该病理相关的临床表现、治疗和预后。一名65岁男性因舌肌束颤和数年构音障碍就诊。体格检查除同侧半侧萎缩外,还发现间歇性右舌肌束颤。增强计算机断层扫描显示右侧颈动脉间隙下方有一个强化的颅底肿块。随后,增强磁共振成像进一步明确了其解剖受累情况和起源部位,从而诊断为VPs。在与患者进一步讨论其临床发现后,决定进行观察和系列影像学检查。颅底副神经节瘤是一种罕见的病理实体,可能对优化管理策略构成具有挑战性的多学科方法。治疗可能因病例而异,取决于患者和肿瘤特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e81f/11379422/6a14d7eb732b/cureus-0016-00000066394-i01.jpg

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