Atypical Focal Choroidal Excavation with Macular Hole in a Patient with Alagille Syndrome.

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2022-09-05 eCollection Date: 2022-01-01 DOI:10.1155/2022/8136115
Manami Misawa, Hironobu Tampo, Shinji Makino
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Abstract

This study is aimed at reporting a rare and unusual focal choroidal excavation with a macular hole in a patient with Alagille syndrome (AGS). A 21-year-old woman with an established early-life AGS diagnosis was referred to our hospital prior to liver transplantation. Examination revealed best-corrected visual acuity of 16/20 and 20/20 in the right and left eye, respectively. Slit-lamp examination was positive for posterior embryotoxon in both eyes. Fundoscopy revealed diffuse choroidal hypopigmentation with increased visibility of the choroidal blood vessels and circumferential chorioretinal atrophy in the mid-peripheral and peripheral retina in both eyes. A full-thickness macular hole with underlying focal choroidal excavation was observed in the right eye. Optical coherence tomography through the macula confirmed choroidal excavation with a full-thickness macular hole in the right eye. To our knowledge, this is the first report describing focal choroidal excavation with a macular hole in an AGS patient.

Abstract Image

Abstract Image

Abstract Image

Alagille综合征患者的非典型局灶性脉络膜挖掘伴黄斑孔1例。
本研究旨在报道一例罕见且不寻常的Alagille综合征(AGS)患者的局灶性脉络膜挖掘伴黄斑孔。一名21岁的女性在肝移植前被诊断为早期生活AGS。检查显示右眼最佳矫正视力16/20,左眼最佳矫正视力20/20。裂隙灯检查双眼后胚胎毒素阳性。眼底镜检查显示双眼中、外周视网膜弥漫性脉络膜色素沉着,脉络膜血管可见性增加,周围脉络膜视网膜萎缩。右眼可见全层黄斑裂孔伴病灶性脉络膜凹陷。通过黄斑的光学相干断层扫描证实了右眼黄斑全层空洞的脉络膜挖掘。据我们所知,这是第一次报道局灶性脉络膜挖掘伴黄斑孔的AGS患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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