Ophthalmology department, University Hospital Waterford, Waterford, Ireland
Ophthalmology department, University Hospital Waterford, Waterford, Ireland.
BMJ Case Rep. 2022 Aug 30;15(8):e249990. doi: 10.1136/bcr-2022-249990.
A man in his 50s presented to the eye emergency department on three separate occasions complaining of blurred vision and discomfort in the left eye. He had a history of Marfan syndrome and had undergone bilateral 20-gauge (G) pars plana vitrectomy and lensectomy 20 years prior for ectopia lentis. On examination he had epithelial corneal oedema, raised intraocular pressure >40 mm Hg and conjunctival chemosis, which later appeared as a bleb-like conjunctival elevation. Acute treatment with oral acetazolamide and topical ocular hypotensive agents produced a marked reduction in intraocular pressure to 2-4 mm Hg. A presumed diagnosis of a leaking scleral wound was made. He underwent scleral exploration under general anaesthesia and a leaking sclerotomy was uncovered. The defect was repaired successfully using a scleral patch graft. Late dehiscence of a sclerotomy has been reported rarely in patients with Marfan syndrome. This is the first reported case to present atypically with intermittent episodes of raised intraocular pressure rather than with hypotony.
一位 50 多岁的男性因左眼视物模糊和不适,在三个不同的场合到眼科急诊就诊。他有马凡综合征病史,20 年前曾因晶状体异位接受过双侧 20G(Gauge)巩膜平坦部玻璃体切除术和晶状体切除术。检查发现上皮性角膜水肿,眼内压升高>40mmHg,伴有结膜水肿,后来出现类似滤泡样结膜隆起。口服乙酰唑胺和局部降眼压药物治疗后,眼内压明显下降至 2-4mmHg。考虑诊断为巩膜伤口漏。他在全身麻醉下进行了巩膜探查,发现巩膜切开处有渗漏。使用巩膜贴片移植成功修复了该缺陷。马凡综合征患者的巩膜切开处迟发性裂开很少见。这是首例报告的不典型病例,表现为间歇性高眼压,而不是低眼压。