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首页> 外文期刊>The Internet journal of neurosurgery >Sudden onset blindness as a presenting feature of chronic subdural haematoma: case report
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Sudden onset blindness as a presenting feature of chronic subdural haematoma: case report

机译:突然发作的失明是慢性硬膜下血肿的表现:病例报告

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We present a rare case report of a patient with chronic subdural haematoma presenting with sudden onset blindness secondary to severe acute bilateral papilloedema. Following prompt surgical evacuation, the patient’s visual acuity returned back to almost normal. Previous reported cases in the literature of blindness following subdural haematomas were related to bilateral homonymous hemianopia due to compression of the posterior cerebral artery following tentorial herniation. These patients were either left blind or developed significant visual deficit despite surgical evacuation. Our case is the first in the literature where the blindness was reversible and due to severe acute papilloedema. There was also no evidence of posterior cerebral artery territory ischaemia. We discuss the importance of visual symptoms in subdural haematoma and emphasize the importance of prompt early intervention. Clinical presentation A 21 years old man was transferred as an emergency from the regional district general hospital after he presented with sudden onset of complete blindness in both eyes in the early hours of the day of transfer. Prior to this, he has been complaining of severe progressive headache with episodic visual blurring over the previous seven weeks. There was nothing of note in previous background history.On examination, he was alert, confused and obeying commands. He was eye opening spontaneously and there were no lateralizing signs. He was completely blind in both eyes and there was evidence of gross papilloedema bilaterally.CT (computerized axial tomography) scan showed a significant left sided acute on chronic subdural haematoma with 1 cm midline shift and also a left middle fossa arachnoid cyst. These findings were confirmed on MR (magnetic resonance) imaging (Fig 1) with MRA (magnetic resonance angiography) ruling out an underlying vascular abnormality.
机译:我们提供了一个罕见的病例报告,即慢性硬脑膜下血肿患者伴有严重急性双侧乳头水肿继发的突发性失明。迅速撤离手术后,患者的视力恢复到几乎正常水平。硬膜下血肿后盲症文献中先前报道的病例与双侧同名偏盲有关,这是由于腱鞘疝后脑后动脉受压所致。尽管进行了手术疏散,这些患者还是失明或出现明显的视力障碍。我们的病例是文献中第一个失明是可逆的并且是由于严重的急性乳头水肿引起的。也没有脑后动脉局部缺血的证据。我们讨论了硬膜下血肿中视觉症状的重要性,并强调了早期早期干预的重要性。临床表现一名21岁的男子在转移当天凌晨出现双眼完全失明的情况后,被紧急转诊至地区综合医院。在此之前,他一直抱怨在过去的七个星期中严重的进行性头痛和发作性的视物模糊。在以前的背景历史中没有什么值得注意的地方。在检查中,他机敏,困惑和服从命令。他自发地睁开眼睛,没有侧倾的迹象。他双眼完全失明,双侧有明显的乳头水肿的证据。CT(计算机轴向断层扫描)扫描显示,慢性硬膜下血肿的中线移位1 cm时左侧明显急性,左侧中窝蛛网膜囊肿也位于左侧。这些发现在MR(磁共振)成像(图1)和MRA(磁共振血管造影)中得到了证实,排除了潜在的血管异常。

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