Deaner Jordan D, Zeft Andrew S, Emami-Naeini Parisa, Lowder Careen Y
Cleveland Clinic Cole Eye Institute, 9500 Euclid Avenue I-32, Cleveland, OH, 44195, USA.
Cleveland Clinic, Pediatric Institute, Division of Rheumatology, USA.
Am J Ophthalmol Case Rep. 2020 Jun 2;19:100763. doi: 10.1016/j.ajoc.2020.100763. eCollection 2020 Sep.
To report a case of visual recovery and vascular reperfusion after vaso-occlusive retinopathy from anti-phospholipid syndrome associated with systemic lupus erythematosus.
A 15-year-old boy with a known diagnosis of systemic lupus erythematosus and a clinically significant anti-phospholipid panel presented with sudden vision loss in the left eye. Examination and ocular imaging revealed signs of vaso-occlusive retinopathy. The patient was immediately started on high dose intravenous steroids, followed by mycophenolate mofetil. He remained on aspirin. After showing no improvement in retinal arteriole and capillary perfusion he was started on therapeutic anti-coagulation with enoxaparin. He regained 20/20 vision. Intravenous fluorescein angiography demonstrated reperfusion of retinal arterioles. Optical coherence tomography angiography showed return of flow in the capillary networks.
We present a case of vaso-occlusive retinopathy in a patient with known systemic lupus erythematosus and a clinically significant anti-phospholipid panel, thus meeting criteria for anti-phospholipid syndrome. He was treated with intravenous methylprednisolone, mycophenolate motefil, aspirin, and enoxaparin. The patient not only had great recovery of visual acuity, but also demonstrated reperfusion of arterioles and reconstitution of flow in the retinal capillary network. These findings suggest that the vaso-occlusive disease is reversible if the diagnosis is made promptly and intensive therapy is initiated.
Currently there are no reported cases of vaso-occlusive retinopathy from APLS and SLE with visual recovery, reperfusion, and return of capillary flow.
报告一例患有系统性红斑狼疮相关抗磷脂综合征的血管闭塞性视网膜病变患者视觉恢复和血管再灌注的病例。
一名15岁男孩,已知患有系统性红斑狼疮且抗磷脂检测结果具有临床意义,出现左眼突然视力丧失。检查和眼部成像显示有血管闭塞性视网膜病变的迹象。患者立即开始接受大剂量静脉注射类固醇治疗,随后使用霉酚酸酯。他继续服用阿司匹林。在视网膜小动脉和毛细血管灌注未见改善后,开始使用依诺肝素进行治疗性抗凝。他恢复了20/20的视力。静脉荧光素血管造影显示视网膜小动脉再灌注。光学相干断层扫描血管造影显示毛细血管网络血流恢复。
我们报告了一例患有已知系统性红斑狼疮且抗磷脂检测结果具有临床意义的血管闭塞性视网膜病变患者,符合抗磷脂综合征的标准。他接受了静脉注射甲泼尼龙、霉酚酸酯、阿司匹林和依诺肝素治疗。患者不仅视力有显著恢复,还显示出小动脉再灌注和视网膜毛细血管网络血流重建。这些发现表明,如果能及时诊断并开始强化治疗,血管闭塞性疾病是可逆的。
目前尚无关于抗磷脂综合征和系统性红斑狼疮导致的血管闭塞性视网膜病变出现视觉恢复、再灌注和毛细血管血流恢复的报道病例。