Papadopoulos Vassilis E, Papadimas George K, Androudi Sofia, Anagnostouli Maria, Evangelopoulos Maria-Eleftheria
First Department of Neurology, School of Medicine, Eginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.
Department of Ophthalmology, University of Thessaly, 41110 Larissa, Greece.
Brain Sci. 2023 Sep 23;13(10):1361. doi: 10.3390/brainsci13101361.
Antibodies to glutamic acid decarboxylase (GAD) have been predominantly associated with stiff-person syndrome (SPS), which is often accompanied by organ-specific autoimmune diseases, such as late-onset type 1 diabetes. Autoimmune retinal pathology in SPS has recently been suggested to coexist in patients suffering from this disease; however, evidence reporting potential treatment options for the neurological and visual symptoms these patients experience remains scarce. We provide a review of the relevant literature, presenting a rare case of a middle-aged woman with autoimmune retinopathy (AIR) followed by stiff-leg syndrome who responded to intravenous immune globulin treatment (IVIg). Our report adds to previously reported data supporting the efficacy of IVIg in SPS spectrum disorders while also proposing the potential effect of IVIg in treating SPS spectrum patients with coexisting AIR.
谷氨酸脱羧酶(GAD)抗体主要与僵人综合征(SPS)相关,该综合征常伴有器官特异性自身免疫性疾病,如迟发性1型糖尿病。最近有研究表明,SPS患者存在自身免疫性视网膜病变;然而,关于这些患者神经和视觉症状潜在治疗方案的报道仍然很少。我们回顾了相关文献,并报告了一例罕见病例,一名中年女性患有自身免疫性视网膜病变(AIR),随后出现僵腿综合征,对静脉注射免疫球蛋白治疗(IVIg)有反应。我们的报告补充了先前报道的数据,支持IVIg在SPS谱系障碍中的疗效,同时也提出了IVIg在治疗合并AIR的SPS谱系患者中的潜在作用。