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与回旋状萎缩相关的黄斑劈裂和黄斑假性裂孔的多模态成像:一例家族报告

Multimodal imaging of foveoschisis and macular pseudohole associated with gyrate atrophy: a family report.

作者信息

Zhioua Braham Imène, Ammous Imen, Maalej Rim, Boukari Majdi, Mili Boussen Ilhem, Errais Khalil, Zhioua Raja

机构信息

Department of Ophthalmology, Charles Nicolle University Hospital, Faculty of medicine of Tunis, University of Tunis-El Manar, 1007, Tunis, Tunisia.

出版信息

BMC Ophthalmol. 2018 Apr 12;18(1):89. doi: 10.1186/s12886-018-0755-9.

Abstract

BACKGROUND

To report the results of multimodal imaging of a biochemically confirmed case of a family with gyrate atrophy (GA) associated with foveoschisis and macular pseudohole.

CASE PRESENTATION

Two sisters presented to us with progressive bilateral decreased vision. The 26-year old sister had a best corrected visual acuity (BCVA) of 20/32 in the right eye (RE) and 20/100 in the left eye (LE). Dilated fundus examination revealed multiple bilateral chorioretinal atrophy areas in the midperipheral and peripheral retina. Fluorescein angiography did not show any leak in the macular area. Swept-source optical coherence tomography (SS-OCT) showed increased central macular thickness in both eyes with foveoschisis. Optical coherence tomography angiography (OCTA) showed petaloid non-reflective areas and some perifoveal microvascular alterations similar to telangiectasias in the deep capillary complex. The 30-year-old sister had a BCVA of 20/20 in the RE and 20/32 in the LE. SS-OCT was normal in the RE and demonstrated a macular pseudohole with a fine epiretinal membrane in the LE. The persistent retinal tissue at the base of the pseudohole was disorganised. Blood tests showed hyperornithinemia in the 2 cases. Based on these observations, the patients were diagnosed with gyrate atrophy of the choroid and retina and were treated with a pyridoxine supplement and an arginine-restricted diet.

CONCLUSIONS

Foveoschisis and macular pseudohole may be associated in GA, increasing the risk of rapid vision loss. OCTA is an interesting imaging tool that can help to better understand the pathophysiological mechanism of these macular involvements in GA.

摘要

背景

报告一例经生化确诊的患有与中心性劈裂和黄斑假性裂孔相关的回旋状萎缩(GA)的家族性病例的多模态成像结果。

病例介绍

两名姐妹前来就诊,均有进行性双侧视力下降。26岁的姐姐右眼最佳矫正视力(BCVA)为20/32,左眼为20/100。散瞳眼底检查发现双眼中周部和周边视网膜有多个双侧脉络膜视网膜萎缩区。荧光素血管造影显示黄斑区无渗漏。扫频光学相干断层扫描(SS-OCT)显示双眼中心黄斑厚度增加伴中心性劈裂。光学相干断层扫描血管造影(OCTA)显示花瓣状无反射区以及一些与深层毛细血管复合体中毛细血管扩张相似的黄斑周围微血管改变。30岁的姐姐右眼BCVA为20/20,左眼为20/32。右眼SS-OCT正常,左眼显示黄斑假性裂孔伴薄的视网膜前膜。假性裂孔底部的残留视网膜组织紊乱。血液检查显示这两名患者均有高鸟氨酸血症。基于这些观察结果,患者被诊断为脉络膜和视网膜回旋状萎缩,并接受了吡哆醇补充剂和精氨酸限制饮食治疗。

结论

中心性劈裂和黄斑假性裂孔可能与GA相关,增加快速视力丧失的风险。OCTA是一种有趣的成像工具,有助于更好地理解GA中这些黄斑病变的病理生理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb4/5897997/9d87c9e23ffa/12886_2018_755_Fig1_HTML.jpg

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