Mizutani Nao, Kato Kumiko, Kashima Yuzen, Matsui Yoshitsugu, Sugimoto Masahiko, Matsubara Hisashi, Kondo Mineo
Department of Ophthalmology, Mie University Graduate School of Medicine, Tsu, Japan.
Department of Ophthalmology and Visual Science, Faculty of Medicine, Yamagata University, Japan.
Am J Ophthalmol Case Rep. 2025 Apr 2;38:102323. doi: 10.1016/j.ajoc.2025.102323. eCollection 2025 Jun.
To report our findings in a rare case of unilateral endophthalmitis caused by in a healthy young man complicated by a rupture of the lens capsule and a rhegmatogenous retinal detachment (RRD).
A 22-year-old Cambodian man presented with recurrent blurry vision in the left eye, following a two-year history of recurrent uveitis initially responsive to corticosteroid treatment. However, during the second recurrence, corticosteroids failed to control the inflammation. At our initial examination, non-granulomatous keratic precipitates, posterior synechiae, and vitreous opacities were observed. Polymerase chain reaction (PCR) of the aqueous humor identified bacterial DNA leading to a suspicion of bacterial endophthalmitis. Vitreous surgery revealed a lens capsule rupture and a giant retinal tear. Retinal photocoagulation and silicone oil tamponade were performed to reattach the retina. Given his occupation at a construction site, ocular trauma was considered. However, preoperative examination and intraoperative findings revealed no evidence of intraocular foreign bodies. Cultures of the vitreous fluid detected . Targeted antibiotic therapy with topical levofloxacin and systemic ciprofloxacin was administered, and the decimal best-corrected visual acuity improved to 1.2 two months post-treatment.
This case highlights the diagnostic and therapeutic challenges posed by rare pathogens such as . Clinicians should be aware of bacterial causes in atypical uveitis particularly in patients refractory to conventional therapy.
报告我们在一名健康年轻男性中罕见的由[病原体名称未给出]引起的单眼眼内炎病例的研究结果,该病例并发晶状体囊破裂和孔源性视网膜脱离(RRD)。
一名22岁的柬埔寨男性,在经历了两年的复发性葡萄膜炎病史,最初对皮质类固醇治疗有反应后,左眼出现反复视力模糊。然而,在第二次复发时,皮质类固醇未能控制炎症。在我们的初次检查中,观察到非肉芽肿性角膜后沉着物、虹膜后粘连和玻璃体混浊。房水的聚合酶链反应(PCR)鉴定出细菌DNA,怀疑为细菌性眼内炎。玻璃体手术显示晶状体囊破裂和巨大视网膜裂孔。进行了视网膜光凝和硅油填充以复位视网膜。考虑到他在建筑工地的工作,怀疑有眼外伤。然而,术前检查和术中发现均未发现眼内异物证据。玻璃体液培养检测到[病原体名称未给出]。给予局部左氧氟沙星和全身环丙沙星的靶向抗生素治疗,治疗后两个月最佳矫正视力提高到1.2。
本病例突出了由[病原体名称未给出]等罕见病原体引起的诊断和治疗挑战。临床医生应意识到非典型葡萄膜炎的细菌病因,特别是对传统治疗难治的患者。