Kennamer-Chapman Ross M, Jampol Lee M, Rajagopal Rithwick
John Hardesty Department of Ophthalmology, Washington University, St. Louis, MO 63110, USA.
Department of Ophthalmology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Retin Cases Brief Rep. 2024 Oct 7. doi: 10.1097/ICB.0000000000001666.
To present a case of worsening maculopathy and vision loss due to vitreopapillary traction associated with an anomalous optic nerve head in a pediatric patient successfully managed with pars plana vitrectomy.
Retrospective case report.
A 13-year-old boy presented with unilateral maculopathy that slowly progressed over a four-year period. As his visual acuity declined, he became increasingly symptomatic. The macular pathology occurred in the setting of vitreopapillary traction overlying multiple congenital optic nerve abnormalities, including a myelinated nerve fiber layer and a Bergmeister papilla. Following pars plana vitrectomy to alleviate the traction, the patient's macular appearance improved, and his vision slowly recovered to baseline.
There are limited reports of congenital optic nerve anomalies associated with vitreopapillary traction and maculopathy among any age group. This report illustrates a pediatric case in which removal of traction on the nerve head by pars plana vitrectomy was the key therapeutic intervention to alleviate the maculopathy.
报告一例因玻璃体乳头牵引伴视神经乳头异常导致黄斑病变和视力丧失加重的儿科患者,经扁平部玻璃体切除术成功治疗。
回顾性病例报告。
一名13岁男孩出现单侧黄斑病变,在四年时间里缓慢进展。随着视力下降,他的症状日益明显。黄斑病变发生在玻璃体乳头牵引覆盖多种先天性视神经异常的情况下,包括有髓神经纤维层和贝格迈斯特乳头。在进行扁平部玻璃体切除术以减轻牵引后,患者的黄斑外观改善,视力缓慢恢复至基线水平。
在任何年龄组中,关于先天性视神经异常与玻璃体乳头牵引及黄斑病变相关的报道都很有限。本报告阐述了一例儿科病例,其中通过扁平部玻璃体切除术解除对视神经乳头的牵引是缓解黄斑病变的关键治疗干预措施。