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Case of acute optic nerve compression caused by tuberculum sellae meningioma with optic canal involvement

机译:伴有视神经管的蝶鞍脑膜瘤引起的急性视神经受压一例

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Abstract: We present detailed ophthalmic findings in a case of tuberculum sellae meningioma with acute visual symptoms due to optic canal involvement. A 62-year-old Japanese woman reported a 1-week history of headaches and blurred vision in her left eye. Her visual acuity was 0.3 in the left eye with no ophthalmoscopic abnormalities. A relative afferent pupillary defect and inferior temporal field defect were found in the left eye. Pattern visual evoked potentials were undetectable in the left eye. Enhanced magnetic resonance imaging showed a 9 mm intracranial lesion around the left optic nerve anterior to the chiasm. She was diagnosed with granulomatous inflammation because of the increased cell counts and protein concentration in the cerebrospinal fluid. She was treated with steroid pulse therapy, and her visual acuity and visual field defect improved to normal in 3 weeks. However, 16 months after the onset, she suffered from headaches again and had a complete loss of vision in her left eye. There was no response to steroid pulse therapy. Enhanced magnetic resonance imaging revealed that the lesion had extended into the left optic canal, and emergency tumor removal surgery was carried out. The histopathological diagnosis was meningioma. One month after the surgery, her left visual acuity improved to 1.2, and her visual field was almost normal. Pattern visual evoked potentials were present but had a prolonged P100 latency of 170 ms. A thinning of the ganglion cell complex was detected by optical coherence tomography. Ophthalmologists should be aware that a small tuberculum sellae meningioma can cause acute visual symptoms due to optic canal involvement. Early consultation with a neurosurgeon is necessary. Visual evoked potentials and optical coherence tomography are sensitive and helpful in following patients with optic nerve compression.
机译:摘要:我们介绍了因视神经管受累而出现急性视觉症状的蝶鞍类脑膜瘤的详细眼科检查结果。一名62岁的日本妇女报告了1周的头痛史和左眼视力模糊。左眼视力为0.3,无检眼镜异常。左眼发现相对传入瞳孔缺损和颞下视野缺损。在左眼中无法检测到图案视觉诱发电位。增强的磁共振成像显示,在前交叉的左视神经周围有9 mm的颅内病变。她被诊断出肉芽肿性炎症,因为脑脊液中细胞计数和蛋白质浓度增加。她接受了类固醇脉冲疗法的治疗,其视力和视野缺损在3周内恢复了正常。然而,发病后16个月,她再次遭受头痛,左眼完全丧失视力。对类固醇脉冲疗法无反应。增强的磁共振成像显示病变已扩展到左视神经管,并进行了紧急肿瘤切除手术。组织病理学诊断为脑膜瘤。手术后一个月,她的左视力提高到1.2,视野几乎正常。存在模式视觉诱发电位,但P100潜伏期延长至170 ms。通过光学相干断层扫描检测神经节细胞复合物的变薄。眼科医生应意识到,小结节性结核性脑膜瘤可因视神经管受累而引起急性视觉症状。尽早与神经外科医生协商是必要的。视觉诱发电位和光学相干断层扫描非常敏感,有助于追踪视神经受压的患者。

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