Sheng Yan, Sun Wen, Shen Ye
Department of Ophthalmology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Medicine (Baltimore). 2019 Aug;98(31):e16577. doi: 10.1097/MD.0000000000016577.
Macular hole (MH) is a rare complication of Terson syndrome. Delayed closure of persistent MH after pars plana vitrectomy (PPV) is occasionally reported in literature, none of them is MH secondary to Terson syndrome. We describe a case of MH secondary to Terson syndrome and delayed closure occurred after PPV, and we also study the characteristics of delayed closure of persistent MH by reviewing related literatures.
A 61-year-old man presented with vitreous hemorrhage in right eye following a subarachnoid hemorrhage due to spontaneous rupture of his right vertebral artery dissecting aneurysm. The visual acuity was hand motion in the right eye and 20/30 in the left eye. Fundus examination showed dense and diffuse vitreous hemorrhage in the right eye.
Terson syndrome was diagnosed according to his subarachnoid hemorrhage history and vitreous hemorrhages in right eye.
PPV combined with phacoemulsification and intraocular lens implantation was performed in his right eye, and internal limiting membrane (ILM) peeling was also performed due to a MH noted during the surgery.
One week after PPV, optical coherence tomography (OCT) showed a persistent MH. Without any intervention, the MH became smaller and flattened, with the best corrected visual acuity (BCVA) improved to 30/200 at 1 month after surgery. Six months later, the MH completely closed with BCVA improved to 20/40. According to our literature review, there are 8 cases of the delayed MH closure, which includes idiopathic MH (4 eyes), traumatic MH (2 eyes), and vitreomacular traction (2 eyes). There is no report about delayed closure of MH secondary to Terson syndrome. The times for these delayed closure occurred following PPV were ranged from 1 to 28 months. Holes even with obviously raised edges after PPV may spontaneously close, just like the case presented here.
Delayed closure of persistent MH after PPV is rarely reported. The significance of this case is to suggest that similar patients should be monitored carefully by OCT, and additional surgery for the MH may be delayed, since delayed closure is possible. The exact mechanisms of delayed closure of persistent MH still need to be clarified.
黄斑裂孔(MH)是Terson综合征的一种罕见并发症。文献中偶尔报道过玻璃体切割术后持续性MH延迟闭合的情况,但均不是继发于Terson综合征的MH。我们描述了1例继发于Terson综合征且在玻璃体切割术后出现延迟闭合的MH病例,并通过回顾相关文献研究持续性MH延迟闭合的特点。
一名61岁男性,因右侧椎动脉夹层动脉瘤自发破裂导致蛛网膜下腔出血后出现右眼玻璃体积血。右眼视力为手动,左眼视力为20/30。眼底检查显示右眼有浓密弥漫性玻璃体积血。
根据其蛛网膜下腔出血病史及右眼玻璃体积血诊断为Terson综合征。
右眼行玻璃体切割联合超声乳化及人工晶状体植入术,术中因发现MH还进行了内界膜(ILM)剥除。
玻璃体切割术后1周,光学相干断层扫描(OCT)显示持续性MH。未经任何干预,MH变小并变平,术后1个月最佳矫正视力(BCVA)提高到30/200。6个月后,MH完全闭合,BCVA提高到20/40。根据我们的文献回顾,有8例延迟的MH闭合病例,包括特发性MH(4只眼)、外伤性MH(2只眼)和玻璃体黄斑牵引(2只眼)。尚无继发于Terson综合征的MH延迟闭合的报道。这些延迟闭合发生在玻璃体切割术后的时间为1至28个月。即使玻璃体切割术后边缘明显隆起的裂孔也可能自发闭合,就像本例。
玻璃体切割术后持续性MH延迟闭合鲜有报道。本例的意义在于提示对于类似患者应通过OCT仔细监测,并且由于可能出现延迟闭合,MH的额外手术可能需要推迟。持续性MH延迟闭合的确切机制仍需阐明。