Case report: Infectious mononucleosis with bilateral retinal haemorrhages under myelin oligodendrocyte glycoprotein antibody-associated disease.

IF 5.7 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1480134
Yuyu Li, Mingming Sun, Shihui Wei, Quangang Xu, Huanfen Zhou
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Abstract

Background: Bilateral optic neuritis associated with optic disc swelling is a common feature of myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). However, extensive deep retinal haemorrhages have not been described in the context of MOG-associated optic neuritis. Here, we report a case of infectious mononucleosis with marked binocular peripapillary and perivascular haemorrhages as well as extensive deep retinal haemorrhages in the presence of MOGAD.

Case report: A 39-year-old Chinese woman presenting with subacute binocular vision reduction with no light perception was diagnosed with MOGAD. Fundus examination revealed the presence of binocular peripapillary and perivascular haemorrhages as well as extensive deep retinal haemorrhages with severe optic disc swelling greater in the right eye than in the left and dilated and tortuous retinal venules. The patient tested positive for the Epstein-Barr virus (EBV) antigen (595 U/mL) and the EBV capsid antigen (>750 U/mL). She had a fever and right upper quadrant abdominal pain, and a doctor determined splenomegaly 1 week before the onset of orbital pain and decreased vision acuity. Medical history and laboratory tests indicated the presence of concurrent infectious mononucleosis. Other investigational indicators of retinal haemorrhages, including hypertension, diabetes mellitus, vascular disease, systemic lupus erythematosus, metabolic disease, and renal or liver dysfunction, were absent.

Discussion: This case suggests that retinal haemorrhage is a possible complication of infectious mononucleosis in the presence of MOGAD.

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病例报告:髓鞘少突胶质细胞糖蛋白抗体相关疾病下的传染性单核细胞增多症伴双侧视网膜出血。
背景:伴有视盘肿胀的双侧视神经炎是髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)的常见特征。然而,在 MOG 相关性视神经炎的病例中,尚未发现广泛的视网膜深层出血。在此,我们报告了一例感染性单核细胞增多症病例,该病例伴有明显的双眼虹膜周围和血管周围出血以及广泛的视网膜深层出血,同时存在 MOGAD:一名 39 岁的中国女性出现亚急性双眼视力下降且无光感,被诊断为 MOGAD。眼底检查发现患者存在双眼毛细血管周围出血以及广泛的视网膜深层出血,右眼视盘肿胀严重,大于左眼,视网膜静脉扩张迂曲。患者的爱泼斯坦-巴尔病毒(EBV)抗原(595 U/mL)和EBV囊抗原(>750 U/mL)检测呈阳性。她曾发烧和右上腹疼痛,在出现眼眶疼痛和视力下降前一周,医生确定她脾脏肿大。病史和实验室检查显示她同时患有传染性单核细胞增多症。其他视网膜出血的检查指标,包括高血压、糖尿病、血管疾病、系统性红斑狼疮、代谢疾病、肝肾功能障碍等均不存在:讨论:本病例表明,视网膜出血是传染性单核细胞增多症(MOGAD)可能出现的并发症之一。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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