Adán Alfredo, Sanmartí Raimon, Burés Anniken, Casaroli-Marano Ricardo P
Department of Ophthalmology, Hospital Clinic de Barcelona, Universidad de Barcelona, Barcelona, Spain.
Am J Ophthalmol. 2007 Mar;143(3):533-4. doi: 10.1016/j.ajo.2006.10.047. Epub 2006 Nov 28.
To report a case of Diffuse Subretinal Fibrosis (DSF) syndrome refractory to immunosuppressive therapy who was successfully treated with anti-tumor necrosis factor-alpha (TNF)-alpha monoclonal antibodies infliximab.
Interventional case report.
A 23-year-old male with bilateral choroiditis presented sudden dimness of vision associated to nasal scotoma in his right eye. Complete ophthalmic examination with appropriated clinical and laboratorial evaluations was carried out during all follow-up. Inform consent statement and Internal Ethics Board approval were also obtained for an open-label therapy schedule.
Extensive temporal subretinal lesion in his right eye and DSF in the left eye were observed. The patient received intravenous infliximab infusion (5 mg/kg) schema. Four weeks after starting treatment his visual acuity improved with decrease in ocular inflammation.
This report describes a case of DSF syndrome that responded remarkably well to infliximab treatment suggesting that TNF-alpha could play an important pathogenetic role in this syndrome.
报告一例对免疫抑制治疗无效的弥漫性视网膜下纤维化(DSF)综合征患者,其通过抗肿瘤坏死因子-α(TNF)-α单克隆抗体英夫利昔单抗成功治疗。
介入性病例报告。
一名23岁双侧脉络膜炎男性患者,右眼突发视力模糊并伴有鼻侧暗点。在整个随访过程中进行了全面的眼科检查以及适当的临床和实验室评估。还获得了知情同意书,并经内部伦理委员会批准采用开放标签治疗方案。
观察到右眼广泛的颞侧视网膜下病变和左眼的DSF。患者接受了静脉注射英夫利昔单抗(5mg/kg)方案。开始治疗四周后,其视力改善,眼部炎症减轻。
本报告描述了一例对英夫利昔单抗治疗反应显著良好的DSF综合征病例,提示TNF-α可能在该综合征中起重要的致病作用。