Secondary Angle-Closure Glaucoma Associated With Congenital Acorea That Developed Into Endophthalmitis After Glaucoma Drainage Implant Surgery: A Case Report
Kenya Yuki, Yumi Matsuura, Mizuki Yaginuma, Takashi Negishi, Masayoshi Shinjoh

TL;DR
A rare case of eye disease in an infant with congenital acorea led to glaucoma and severe infection after surgery.
Contribution
This case report documents a rare association between congenital acorea and secondary angle-closure glaucoma with postoperative endophthalmitis.
Findings
Secondary angle-closure glaucoma developed in an infant with congenital acorea.
Glaucoma drainage implant surgery led to endophthalmitis caused by Haemophilus influenzae.
The case highlights risks of severe complications following glaucoma surgery in infants with acorea.
Abstract
We report a rare case of unilateral secondary angle-closure glaucoma associated with congenital acorea in a 10-month-old male infant. Acorea is a rare congenital eye abnormality characterized by the complete absence of the pupil. The left cornea of this patient measured 13.0 mm vertically and horizontally, with opacities observed. The anterior chamber was absent, and the pupil was completely occluded. Intraocular pressure (IOP) was 26 mmHg, and axial length was 25.3 mm. The fundus was not visible due to acorea. The patient was diagnosed with secondary angle-closure glaucoma due to acorea. To relieve angle closure, a pupil was created under general anesthesia. After blunt dissection with viscoelastic, a vitreous cutter was inserted through a corneal incision, and central iridectomy was performed. Anterior chamber depth was normalized immediately. Despite initial surgical pupil formation…
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Taxonomy
TopicsOcular Disorders and Treatments · Glaucoma and retinal disorders · Intraocular Surgery and Lenses
