Hanna Verina, Mednick Zale, Micieli Jonathan
Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada.
BMJ Case Rep. 2021 May 6;14(5):e241850. doi: 10.1136/bcr-2021-241850.
A 49-year-old man presented with new onset headache and diplopia, with right ptosis and limitation of extraocular movements consistent with a third nerve palsy. He had a known diagnosis of a non-functioning pituitary adenoma, and his presentation and neuroimaging were consistent with ischaemic pituitary apoplexy. The patient was otherwise stable with no signs of optic neuropathy or endocrine abnormality. He was observed with close interval follow-up and reported resolution of symptoms within 4 days after onset. Pituitary apoplexy is a potentially life-threatening condition often managed with initial medical stabilisation followed by neurosurgical decompression. The guidelines regarding the utility of surgery in patients with isolated ocular motility disorders are unclear, and recent retrospective studies suggested that outcomes may be similar in patients managed conservatively. This case demonstrates that rapid resolution of an isolated third nerve palsy may occur in this setting, and that observation is a reasonable initial management strategy.
一名49岁男性出现新发头痛和复视,伴有右侧上睑下垂及眼外肌运动受限,符合动眼神经麻痹表现。他已知患有无功能性垂体腺瘤,其临床表现及神经影像学检查结果均符合缺血性垂体卒中。该患者其他方面情况稳定,无视神经病变或内分泌异常迹象。对其进行密切随访观察,患者在发病后4天内症状消失。垂体卒中是一种潜在的危及生命的疾病,通常先进行药物初始稳定治疗,随后进行神经外科减压手术。关于手术在孤立性眼球运动障碍患者中的应用价值,相关指南并不明确,近期的回顾性研究表明,保守治疗患者的预后可能相似。该病例表明,在此情况下孤立性动眼神经麻痹可能迅速缓解,观察是一种合理的初始治疗策略。