Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
PLoS One. 2024 Aug 29;19(8):e0309686. doi: 10.1371/journal.pone.0309686. eCollection 2024.
Skull base tumors, can cause oculomotor dysfunction, presenting a management challenge given their proximity to cranial nerves. This study investigated the oculomotor outcomes in patients with skull base tumors presenting cranial nerve palsy due to tumor compression and aimed to identify associated factors.
This retrospective observational cohort study enrolled patients diagnosed with primary skull base tumors who exhibited cranial nerve palsy due to tumor compression, confirmed by magnetic resonance imaging treated at Asan Medical Center between January 2011 and December 2022. Patients were assessed for oculomotor function pre- and post-treatment, and categorized into recovery and non-recovery groups based on outcomes. Factors associated with oculomotor outcomes were also analyzed.
Fifty-six patients were enrolled, with the majority (n = 37, 66.1%) demonstrating recovery in oculomotor function post-treatment. The duration from symptom onset to treatment initiation was short in the recovery group, suggesting that early treatment may contribute to improved oculomotor outcomes. The type of tumor was significantly associated with oculomotor outcomes, with patients with pituitary adenoma exhibiting better outcomes. In the recovery group, 19/37 (51.4%) patients underwent surgical resection alone. In contrast, in the non-recovery group, 17/19 (89.5%) patients received primary or adjuvant radiosurgery or radiation therapy.
Approximately 70% of patients with skull base tumors experienced recovery in oculomotor function post-treatment. The duration before treatment and the type of tumor were significantly associated with the oculomotor outcome. These findings aid neuro-ophthalmologists in predicting oculomotor outcomes for patients with skull base tumors, guiding management strategies for oculomotor dysfunction.
颅底肿瘤可导致动眼神经功能障碍,由于其与颅神经毗邻,因此对其管理具有挑战性。本研究调查了因肿瘤压迫而出现颅神经麻痹的颅底肿瘤患者的动眼神经功能结果,并旨在确定相关因素。
这项回顾性观察性队列研究纳入了 2011 年 1 月至 2022 年 12 月期间在 Asan 医疗中心接受治疗的因肿瘤压迫而出现颅神经麻痹(经磁共振成像证实)的原发性颅底肿瘤患者。在治疗前后对患者的动眼神经功能进行评估,并根据结果分为恢复组和未恢复组。还分析了与动眼神经结果相关的因素。
共纳入 56 例患者,其中大多数(n=37,66.1%)在治疗后动眼神经功能恢复。恢复组从症状出现到开始治疗的时间较短,表明早期治疗可能有助于改善动眼神经结果。肿瘤类型与动眼神经结果显著相关,垂体腺瘤患者的结果更好。在恢复组中,37 例患者中有 19 例(51.4%)单独接受了手术切除。相比之下,在未恢复组中,19 例中有 17 例(89.5%)患者接受了原发或辅助放射外科手术或放疗。
约 70%的颅底肿瘤患者在治疗后动眼神经功能恢复。治疗前的时间和肿瘤类型与动眼神经结果显著相关。这些发现有助于神经眼科医生预测颅底肿瘤患者的动眼神经结果,指导动眼神经功能障碍的管理策略。