垂体大腺瘤合并中风,模拟正常张力型青光眼1例。

IF 0.2 Q4 OPHTHALMOLOGY
Thinley, Keepa Vaidya, Sandip Tamang
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引用次数: 0

摘要

背景:类似青光眼损害的高杯盘比的不对称视野缺损可能是垂体大腺瘤合并中风的唯一临床特征,这给诊断带来了挑战。病例:一名39岁男性,右视野渐进性视力模糊1个月,无其他神经系统症状。经检查,他的双眼眼压(IOP)为16 mmHg。后节检查显示右眼杯盘比(CDR)为0.8,左眼为0.7,同心圆神经视网膜边缘变薄,轻度颞盘苍白。这些发现为其他地方的正常张力性青光眼(NTG)的诊断和治疗提供了依据。视野检查显示视野缺损,以交界暗点为特征。脑部核磁共振扫描显示位于鞍区一界限清楚的肿块,提示垂体大腺瘤,后经组织病理学检查证实可能为中风。神经外科团队通过鼻内窥镜经蝶窦入路成功切除肿瘤,患者报告视力和视野缺损有明显改善。观察:在我们的病例中,视觉体征和症状是唯一的表现特征,由垂体大腺瘤合并中风引起,这可能是一种潜在的危及生命的疾病。虽然垂体性中风是一种急性疾病,伴有许多神经系统体征和症状,但本病例仅表现为高CDR的视觉症状和神经视网膜边缘变薄及轻度颞盘苍白,这对诊断提出了挑战。没有相关的全身表现。然而,由于及时诊断和多学科治疗,患者预后良好。结论:垂体大腺瘤合并中风的临床表现应包括渐进性、渐进性视野不对称缺损伴颞盘苍白,便于及时诊断和有效治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pituitary Macroadenoma with Apoplexy, a Mimicker of Normal Tension Glaucoma (NTG): A Case Report.

Background: Asymmetric visual field defects with a high cup-to-disc ratio resembling glaucomatous damage can be the only clinical features of a pituitary macroadenoma with apoplexy, posing diagnostic challenges.

Case: A 39-year-old man presented with a history of gradual onset, progressive visual obscuration in the right visual field for one month without any other accompanying neurological symptoms. On examination, his intraocular pressure (IOP) was 16 mmHg in both eyes. Posterior segment examination revealed a cup to-disc ratio (CDR) of 0.8 in the right and 0.7 in the left eye, with concentric neuroretinal rim thinning and mild temporal disc pallor. These findings led to the diagnosis and treatment of normal tension glaucoma (NTG) elsewhere. Visual field examination showed field defects featuring a junctional scotoma. The MRI scan of the brain revealed a well-defined mass lesion situated in the sella suggestive of pituitary macroadenoma with possible apoplexy confirmed later through histopathological examination. The neurosurgery team successfully removed the tumor through the endoscopic endonasal trans-sphenoidal approach and the patient reported significant improvement in vision and visual field defects.

Observations: In our case, visual signs and symptoms were the only presenting features, caused by pituitary macroadenoma with apoplexy, which can be a potentially life-threatening condition. Although pituitary apoplexy is an acute condition with numerous neurological signs and symptoms, visual symptoms with high CDR and neuroretinal rim thinning with mild temporal disc pallor were the only features seen in our case, posing a diagnostic challenge. There were no associated systemic manifestations. However, the patient had a favorable outcome because of prompt diagnosis and multidisciplinary management.

Conclusion: The spectrum of clinical manifestations of pituitary macroadenoma with apoplexy should encompass a gradual onset, progressive asymmetric visual field defect with temporal disc pallor to facilitate timely diagnosis and effective management.

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