Toh Zhi Hong, Agrawal Rupesh
National Healthcare Group Eye Institute, Tan Tock Seng Hospital, Singapore.
Am J Ophthalmol Case Rep. 2020 Jan 7;17:100589. doi: 10.1016/j.ajoc.2020.100589. eCollection 2020 Mar.
To report a case of a 28-years-old male who presented with a worsening unilateral panuveitis after intensive topical steroid therapy which resulted in a diagnostic and treatment dilemma as to whether the patient should be treated as for infective endophthalmitis despite no immediate known infective risk factors.
A patient presented initially with unilateral non-granulomatous acute anterior uveitis which worsened after being started on intensive steroid therapy, developing fibrinous panuveitis. The rapid worsening of inflammation and vision deterioration despite being on intensive steroid therapy resulted in the patient subsequently being treated as for infective endophthalmitis. Anterior chamber and vitreous tap were done and intravitreal antibiotics were administered, along with topical antibiotics therapy. Vitrectomy was withheld due to the lack of conclusive evidence of infective etiology and risk factors. Full uveitis and infective workup were done. Investigations were largely unremarkable, and fluid and vitreous cultures were negative. HLA B27 was positive. The patient was subsequently started on systemic oral corticosteroids and improved in terms of his visual acuity, signs and symptoms.
HLA B27-associated uveitis can present in a range of clinical spectrum with the extreme being of unusual severity in the form of fibrinous panuveitis that can mimic infective endophthalmitis. This can lead to a dilemma in management and subject patients to unnecessary risks from diagnostic and therapeutic interventions. Patients under this subgroup may require long term systemic immunosuppression therapy for disease remission and will require long term follow up.
报告一例28岁男性患者,在强化局部类固醇治疗后出现单侧葡萄膜炎加重,这导致了诊断和治疗上的两难困境,即尽管没有直接已知的感染危险因素,但该患者是否应按感染性眼内炎进行治疗。
一名患者最初表现为单侧非肉芽肿性急性前葡萄膜炎,在开始强化类固醇治疗后病情恶化,发展为纤维蛋白性全葡萄膜炎。尽管接受了强化类固醇治疗,但炎症迅速加重和视力下降,导致该患者随后按感染性眼内炎进行治疗。进行了前房和玻璃体穿刺,并给予玻璃体内抗生素以及局部抗生素治疗。由于缺乏感染病因和危险因素的确切证据,未进行玻璃体切除术。进行了全面的葡萄膜炎和感染方面的检查。检查结果大多无异常,房水和玻璃体培养均为阴性。HLA B27呈阳性。该患者随后开始接受全身性口服皮质类固醇治疗,视力、体征和症状均有所改善。
HLA B27相关的葡萄膜炎可表现出一系列临床症状,极端情况是表现为不寻常的严重程度,即纤维蛋白性全葡萄膜炎,可模仿感染性眼内炎。这可能导致管理上的两难困境,并使患者面临诊断和治疗干预带来的不必要风险。该亚组患者可能需要长期全身性免疫抑制治疗以实现疾病缓解,并且需要长期随访。