Case Report: Congenital Pseudoacorea in an Ocular Axenfeld-Rieger Syndrome: What is it?

Journal of clinical cases & reports Pub Date : 2023-10-01 Epub Date: 2023-03-28 DOI:10.46619/joccr.2023.6-1145
Andrés Germán Alza
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Abstract

Summary: This is a descriptive summary of the case of a patient with Axenfeld-Rieger syndrome associated with a congenital malformation of the iris and consequent pupillary morphological alteration of an atypical characteristic reported. This anomaly is unique in scientific literature and exhibits a peculiarity that we have called pseudoacorea: Hidden pupil. Other associated abnormal clinical findings were posterior embryotoxon, astigmatism, amblyopia, and exotropia. Diagnosis was achieved by instilling ocular mydriatics into the cul-de-sac that revealed this peculiarity. It is necessary to make a differential diagnosis with other pupillary pathologies such as corectopia, acorea and microcoria. Early detection of pathology and surgical management is necessary, since it would lead to a better visual prognosis for both amblyopia and strabismus.

Background: Among the malformations of the pupil, we can find polycoria (more than one pupil), dyscoria (abnormal pupil shape), corectopia (abnormal pupil position) and acorea (absence of pupil). In addition, morphologically normal pupils can denote other anomalies such as the microcoria described by Holth in 1923. Acorea is a rare anomaly, congenital or acquired, characterized by an absolute absence of the pupil both at rest and in mydriasis. In our case we prefer to differentiate it and name it pseudoacorea, since although there is a total absence of the pupil at rest thanks to the application of ocular mydriatics, a micropupil with discoric and corectopic characteristics is achieved. It is worth noting that we have not detected in the scientific literature any case described as the one that we will develop here.

Conclusion: The case of a patient with Axenfeld-Rieger syndrome associated with a congenital malformation of the iris and consequent atypical pupillary morphological alteration is presented. This anomaly is unique in the scientific literature and presents a peculiarity that we have called pseudoacorea: Hidden pupil. Early detection of pathology and surgical management is necessary, since it would lead to a better visual prognosis for both amblyopia and strabismus.

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眼部Axenfeld-Rieger综合征的先天性假橡子:是什么?
摘要:这是一例Axenfeld-Rieger综合征患者的描述性总结,该患者伴有先天性虹膜畸形,随后瞳孔形态发生非典型改变。这种异常现象在科学文献中是独一无二的,并表现出一种我们称之为假橡子的特性:隐藏的瞳孔。其他相关的异常临床表现为后胚胎中毒、散光、弱视和外斜视。诊断是通过向死胡同滴注眼球瞳孔管来实现的,这揭示了这一特点。有必要与其他瞳孔病变进行鉴别诊断,如远视、橡实和小瞳孔。早期发现病理和手术治疗是必要的,因为这将导致弱视和斜视更好的视觉预后。背景:在瞳孔的畸形中,我们可以发现多发性瞳孔畸形(不止一个瞳孔)、斜视(瞳孔形状异常)、远视(瞳孔位置异常)和橡实(瞳孔缺失)。此外,形态正常的瞳孔可以表示其他异常,例如Holth在1923年描述的微瞳孔。Acorea是一种罕见的先天性或后天性异常,其特征是在休息和散瞳时瞳孔完全缺失。在我们的案例中,我们更喜欢将其区分开来,并将其命名为假橡子,因为尽管由于应用了眼部mydriatics,在静止时完全没有瞳孔,但还是获得了具有盘状和共视特征的微瞳孔。值得注意的是,我们在科学文献中没有发现任何我们将在这里开发的案例。结论:报告了一例Axenfeld-Rieger综合征患者,该综合征伴有先天性虹膜畸形和由此引起的非典型瞳孔形态改变。这种异常现象在科学文献中是独一无二的,并呈现出一种我们称之为假橡子的特性:隐藏的瞳孔。早期发现病理和手术治疗是必要的,因为这将导致弱视和斜视更好的视觉预后。
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