Sudden onset blindness as a presenting feature of chronic subdural haematoma: case report

S. Kabir, A. A. Kamat, T. Carroll
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Abstract

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. Figure 1 Fig 1: MRI scan showing chronic subdural haematoma causing midline shift. There is also a left temporal arachnoid cyst Considering the papilloedema and scan appearances, he underwent emergency burrhole drainage of subdural haematoma on the evening of transfer. He had significant recovery of his vision within 24 hours of his surgery. Visual acuity has been recorded as 6/9 right eye, 6/12 left eye with good fields in Goldman perimetry but with enlarged blind spots bilaterally. He was subsequently discharged home and at the time of discharge, he was self caring, alert, oriented and had not suffered any deficits a result of the surgery. On review in the outpatient clinic in 6 weeks time, his visual acuity in the right eye was 6/6+2 and left eye 6/9+1. Repeat CT scan (Fig 2) showed that the Sudden onset blindness as a presenting feature of chronic subdural haematoma: case report 2 of 4 subdural haematoma had resolved and the arachnoid cyst was unchanged.
慢性硬膜下血肿的表现为突发性失明1例
我们提出一个罕见的病例报告,病人慢性硬膜下血肿提出突然失明继发于严重的急性双侧乳头水肿。经过及时的手术疏散,患者的视力恢复到几乎正常。以往文献报道的硬膜下血肿致盲病例与脑幕疝后大脑后动脉受压所致双侧同质性偏盲有关。这些患者要么失明,要么在手术后出现明显的视力缺陷。我们的病例是文献中第一个失明是可逆的,由于严重的急性乳头状水肿。也没有脑后动脉区域缺血的证据。我们讨论硬膜下血肿的视觉症状的重要性,并强调及时早期干预的重要性。临床表现:一名21岁男子在转院当天凌晨突然出现双眼完全失明,作为急诊从地区综合医院转院。在此之前,他在过去的七周内一直抱怨严重的进行性头痛和间歇性视力模糊。在以前的背景历史中没有什么值得注意的。在检查时,他是警觉的,混乱的,服从命令。他的眼睛是自发睁开的,没有偏侧的迹象。他双眼完全失明,双侧有明显的乳头状水肿。CT(计算机轴位断层扫描)显示明显的左侧急性慢性硬膜下血肿,中线移位1厘米,还有左侧中窝蛛网膜囊肿。这些发现在MR(磁共振)成像(图1)和MRA(磁共振血管造影)上得到证实,排除了潜在的血管异常。图1:MRI扫描显示慢性硬膜下血肿引起中线移位。考虑到乳头状水肿和扫描表现,患者于转移当晚紧急行硬膜下血肿钻孔引流术。手术后24小时内,他的视力明显恢复。右眼视力6/9,左眼6/12,Goldman验光视野良好,但双侧盲点增大。他随后出院回家,出院时,他自我照顾,警觉,有方向感,没有任何手术造成的缺陷。6周后复查门诊,右眼视力6/6+2,左眼视力6/9+1。重复CT扫描(图2)显示,慢性硬膜下血肿以突发性失明为表现特征:4例报告2例硬膜下血肿消退,蛛网膜囊肿未见改变。
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