Suppr超能文献

病例报告:一名与肌纤蛋白(MYOC)基因相关的重度青少年开角型青光眼(JOAG)患者视盘杯状凹陷的逆转及随后恢复情况

Case Report: Reversal and subsequent return of optic disc cupping in a myocilin (MYOC) gene-associated severe Juvenile Open-Angle Glaucoma (JOAG) patient.

作者信息

El Helwe Hani, Samuel Sandy, Gupta Sanchay, Neeson Cameron, Chachanidze Marika, Solá-Del Valle David A

机构信息

Glaucoma Service, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, 02114, USA.

Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, 02115, USA.

出版信息

F1000Res. 2022 Nov 22;11:1361. doi: 10.12688/f1000research.127871.1. eCollection 2022.

Abstract

To our knowledge, this case report describes the first instance of reversal of glaucomatous optic nerve cupping in a young adult with a rare form of juvenile open-angle glaucoma (JOAG) associated with a novel variant of the myocilin gene (MYOC). This 25-year-old woman with severe-stage MYOC-associated JOAG presented with blurry vision and intermittent pain in her left eye. She had a strong family history of glaucoma in multiple first-degree relatives with an identified novel variant of MYOC. Examination revealed intraocular pressures (IOPs) of 10 mmHg OD and 46 mmHg OS, with cup-to-disc ratios of 0.90 and 0.80. The patient experienced substantial reversal of optic disc cupping OS following dramatic IOP reduction with trabeculectomy, and subsequently experienced a return of cupping after an IOP spike 15 months postoperatively. The reversal of cupping did not correspond to any changes in the patient's visual field. After an initial decrease in retinal nerve fiber layer (RNFL) thickness, RNFL remained stable for over 2 years after trabeculectomy as seen on Optical Coherence Tomography (OCT). This case suggests reversal of cupping can occur well into adulthood in a MYOC-associated JOAG patient, and it demonstrates the potential bidirectionality of this phenomenon. Moreover, it suggests that these structural changes may not correspond to any functional changes in visual fields or RNFL thickness.

摘要

据我们所知,本病例报告描述了一名患有罕见型青少年开角型青光眼(JOAG)且与肌纤蛋白基因(MYOC)新变体相关的年轻成人中青光眼性视神经杯凹逆转的首例情况。这名25岁患有严重阶段MYOC相关JOAG的女性,左眼出现视力模糊和间歇性疼痛。她在多个一级亲属中有强烈的青光眼家族病史,且已鉴定出MYOC的新变体。检查发现右眼眼压(IOP)为10 mmHg,左眼为46 mmHg,杯盘比分别为0.90和0.80。患者在小梁切除术后眼压大幅降低后,左眼视盘杯凹出现显著逆转,随后在术后15个月眼压升高后杯凹又恢复。杯凹的逆转与患者视野的任何变化均不对应。在视网膜神经纤维层(RNFL)厚度最初下降后,小梁切除术后超过2年,经光学相干断层扫描(OCT)观察,RNFL保持稳定。该病例表明,在MYOC相关JOAG患者中,杯凹逆转可在成年期发生,且证明了这种现象可能具有双向性。此外,这表明这些结构变化可能与视野或RNFL厚度的任何功能变化均不对应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9e/11167334/b5f1fce5dff0/f1000research-11-140417-g0000.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验