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首页> 外文期刊>American Journal of Ophthalmology Case Reports >Submacular choroiditis in common variable immunodeficiency associated with a pathogenic mutation in the tumor necrosis factor gene
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Submacular choroiditis in common variable immunodeficiency associated with a pathogenic mutation in the tumor necrosis factor gene

机译:癌性脉络膜炎与肿瘤坏死因子基因致病性突变相关的常见变量免疫缺陷

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PurposeTo report on a case of submacular choroiditis in a patient with common variable immunodeficiency (CVID).ObservationsAn 80-year-old man was referred with a diagnosis of a central retinal vein occlusion with CME and later developed intraocular inflammation. History was notable for recurrent bacterial infections and myelodysplastic syndrome known to be due to CVID. Ophthalmic examination and multimodal imaging revealed mild intraocular inflammation, retinal vasculitis, submacular choroiditis, and CME. Genetic testing identified a point mutation in TNFRSF13B, a pathogenic variant in the tumor necrosis factor gene known to be associated with CVID, but not with CVID-associated uveitis.Conclusions and importanceThe diagnosis of CVID should be considered in patients with uveitis and a history of recurrent bacterial infections. Genetic testing can support the diagnosis.
机译:关于患有常见可变免疫缺陷患者患者患者囊肿脉络膜炎的PURPOSETO报告(CVID).observationsan 80岁男性,诊断CME和后来产生的眼内炎症的中央视网膜静脉闭塞的诊断。 历史对于已知由CVID的复发细菌感染和髓细胞增强术综合征是值得注意的。 眼科检查和多峰成像显示出轻度眼内炎症,视网膜血管炎,囊状脉络膜炎和CME。 遗传检测鉴定了TNFRSF13B中的点突变,已知与CVID相关的肿瘤坏死因子基因中的病原变异,但不适用于CVID相关的葡萄膜炎。应考虑葡萄膜炎的患者和历史衰退的联系和进一步的CVID诊断 经常性细菌感染。 基因检测可以支持诊断。

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