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双侧钱德勒综合征、小眼球和闭角型青光眼:一种复杂的表现、具有挑战性的诊断及病理洞察——病例报告

Bilateral Chandler Syndrome, Nanophthalmos, and Angle Closure Glaucoma: A Complex Presentation, Challenging Diagnosis, and Pathological Insight-A Case Report.

作者信息

Ismail Ahmed Ameen, El-Ruby Sarah Abdel-Fattah

机构信息

Department of Ophthalmology, Faculty of Medicine, Fayoum University, Al Fayoum, Egypt.

出版信息

J Curr Glaucoma Pract. 2024 Apr-Jun;18(2):68-73. doi: 10.5005/jp-journals-10078-1444. Epub 2024 Jul 10.

DOI:10.5005/jp-journals-10078-1444
PMID:39144732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11320760/
Abstract

AIM AND BACKGROUND

Chandler syndrome (CS) is one of the iridocorneal endothelial syndromes (ICEs) with proliferation of abnormal corneal endothelial cells over the anterior chamber (AC) angle and iris, resulting in complications, for example, secondary angle closure glaucoma (SACG). We report an association between CS and nanophthalmos, highlighting diagnostic and therapeutic challenges and pathological insights.

CASE DESCRIPTION

A 46-year-old female patient presented with bilateral progressive blurring of vision. Examination revealed bilateral (OU) small corneal diameter, shallow AC, closed AC angle, beaten-bronze appearance of corneal endothelium, and mild iris atrophy in the right eye (OD). Intraocular pressure was 48 mm Hg and 22 mm Hg in the OD and left eye (OS), respectively. Fundus examination revealed optic nerve head cupping. Biometry showed short axial length and microcornea OU, that is, nanophthalmos. Optical coherence tomography and visual field revealed structural and functional evidence of glaucomatous optic neuropathy. Specular microscopy demonstrated reduction of corneal endothelial cell density and the light-dark reversal characteristic of ICE. Therefore, a diagnosis of CS with SACG and nanophthalmos was made. The patient was referred to a specialized glaucoma center with recommendation of clear lens extraction and a glaucoma drainage device with retropupillary tube placement.

CONCLUSION

This is the first report of an association between CS and nanophthalmos. It highlights the possibility of SACG despite evident risk factors for primary angle closure glaucoma (PACG). Furthermore, it provides a hypothesis about the etiology of ICE. The concurrence of CS and nanophthalmos suggests that a common developmental mechanism could be implicated since periocular mesenchyme, the embryological precursor of corneal endothelium, plays a role in the development of optic cup and stalk.

CLINICAL SIGNIFICANCE

SACG should be considered even in the presence of evident risk factors for PACG, such as nanophthalmos. Additionally, the association of nanophthalmos and CS warrants revisiting the yet inconclusive etiology of CS, where a developmental mechanism could be considered.

HOW TO CITE THIS ARTICLE

Ameen Ismail A, El-Ruby SA. Bilateral Chandler Syndrome, Nanophthalmos, and Angle Closure Glaucoma: A Complex Presentation, Challenging Diagnosis, and Pathological Insight-A Case Report. J Curr Glaucoma Pract 2024;18(2):68-73.

摘要

目的与背景

钱德勒综合征(CS)是虹膜角膜内皮综合征(ICEs)之一,异常角膜内皮细胞在前房角和虹膜处增殖,导致并发症,例如继发性闭角型青光眼(SACG)。我们报告了CS与小眼球症之间的关联,强调了诊断和治疗挑战以及病理学见解。

病例描述

一名46岁女性患者出现双侧进行性视力模糊。检查发现双侧角膜直径小、前房浅、房角关闭、角膜内皮呈铜击样外观,右眼(OD)有轻度虹膜萎缩。右眼眼压为48 mmHg,左眼(OS)眼压为22 mmHg。眼底检查发现视神经乳头凹陷。生物测量显示双侧眼轴短和小角膜,即小眼球症。光学相干断层扫描和视野检查显示有青光眼性视神经病变的结构和功能证据。镜面显微镜检查显示角膜内皮细胞密度降低以及ICE的明暗反转特征。因此,诊断为伴有SACG和小眼球症的CS。该患者被转诊至专业青光眼中心,建议行透明晶状体摘除术并植入带瞳孔后引流管的青光眼引流装置。

结论

这是CS与小眼球症之间关联的首例报告。它强调了尽管存在原发性闭角型青光眼(PACG)的明显危险因素,但仍有发生SACG的可能性。此外,它提供了一个关于ICE病因的假设。CS与小眼球症的同时出现表明可能涉及共同的发育机制,因为眼周间充质作为角膜内皮的胚胎前体,在视杯和视柄的发育中起作用。

临床意义

即使存在PACG的明显危险因素,如小眼球症,也应考虑SACG。此外,小眼球症与CS的关联值得重新审视尚未明确的CS病因,其中可考虑发育机制。

如何引用本文

Ameen Ismail A, El-Ruby SA. 双侧钱德勒综合征、小眼球症和闭角型青光眼:一例复杂病例、具有挑战性的诊断及病理学见解——病例报告。《当代青光眼实践杂志》2024;18(2):68 - 73。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/1f0159d9a6b1/jocgp-18-2-68-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/4b32165f0e02/jocgp-18-2-68-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/0c845e543c0a/jocgp-18-2-68-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/5d3029edfbbb/jocgp-18-2-68-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/94b059ba8f8d/jocgp-18-2-68-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/9f1340ac92e6/jocgp-18-2-68-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/1f0159d9a6b1/jocgp-18-2-68-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/4b32165f0e02/jocgp-18-2-68-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/0c845e543c0a/jocgp-18-2-68-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/5d3029edfbbb/jocgp-18-2-68-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/94b059ba8f8d/jocgp-18-2-68-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/9f1340ac92e6/jocgp-18-2-68-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/11320760/1f0159d9a6b1/jocgp-18-2-68-g006.jpg

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