Alhamoud Mustafa A, Alnosair Ghadah H, Alhashim Hassan Y
Ophthalmology, King Fahd Hospital of the University, Dammam, SAU.
Pediatric Ophthalmology, Dammam Medical Complex, Dammam, SAU.
Cureus. 2022 Feb 15;14(2):e22256. doi: 10.7759/cureus.22256. eCollection 2022 Feb.
The aim of this study is to share our experience of a baby boy patient who presented with rare endogenous endophthalmitis that ended up with exudative retinal detachment; emphasizing the clinical presentation, follow-ups progression, and the management plan. A case report of a one-month-old preterm baby boy presented with eye discharge in his left eye (OS) associated with eyelid swelling and chemosis for four days. His clinical examination revealed a congested left eye with proptosis, absent red reflex, and normal intraocular pressure (IOP) while a portable slit-lamp examination showed an edematous left eye with cloudy cornea but no infiltrates and no view to the posterior segment. Blood, cerebrospinal fluid (CSF), and ocular discharge were cultured, and all came negative and the patient started on empirical antibiotics. B-scan shows dense infiltrates in the vitreous cavity with subretinal fluid. Diagnostic intravitreal paracentesis was done which showed the growth of and a diagnosis of endogenous endophthalmitis is made then a directed management plan was initiated. Unfortunately, a few days later a repeated B-scan was ordered to the left eye and it shows exudative retinal detachment, and a referral to retinal surgery service was consulted. After further follow-ups, B-scan showed resolving retinal detachment with a short shrunken eye, marked ocular wall thickening, and a relatively short axial length which is consistent with prephthisical changes hence, an oculoplasty referral was done for ocular prosthesis later on. Endogenous endophthalmitis is a rarely encountered intraocular infection yet it carries devastating consequences that may threaten vision. Therefore, a high index of suspicion is essential for early detection of the disease to prevent serious complications and achieve good visual outcomes.
本研究的目的是分享我们对一名男婴患者的治疗经验,该患者患有罕见的内源性眼内炎,最终导致渗出性视网膜脱离;重点介绍临床表现、随访进展及治疗方案。报告一例1个月大的早产男婴,其左眼(OS)出现眼部分泌物,伴有眼睑肿胀和球结膜水肿,持续4天。临床检查发现左眼充血、眼球突出、无红光反射且眼压(IOP)正常,便携式裂隙灯检查显示左眼水肿、角膜混浊,但无浸润,无法观察到眼后段。对血液、脑脊液(CSF)和眼部分泌物进行培养,结果均为阴性,患者开始接受经验性抗生素治疗。B超显示玻璃体腔有密集浸润及视网膜下液。进行了诊断性玻璃体穿刺,结果显示有[具体细菌名称未给出]生长,从而诊断为内源性眼内炎,随后启动了针对性的治疗方案。不幸的是,几天后对左眼进行了重复B超检查,结果显示渗出性视网膜脱离,于是转诊至视网膜手术科室进行会诊。经过进一步随访,B超显示视网膜脱离消退,眼球短小萎缩,眼壁明显增厚,眼轴长度相对较短,这与眼球痨前期改变相符,因此随后转诊至眼部整形科室以安装义眼。内源性眼内炎是一种罕见的眼内感染,但它会带来严重后果,可能威胁视力。因此,高度的怀疑指数对于早期发现该病以预防严重并发症并取得良好的视觉效果至关重要。