3岁非洲女童儿童性眼部重症肌无力1例报告。

IF 0.6 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmology Pub Date : 2025-05-23 eCollection Date: 2025-01-01 DOI:10.1159/000546374
Elisamia Ngowi, Humrath Lusheke, Rashid Mbuma, Zeenat Juneja, Mayila Mbuki, Sheliza Parvez Thaver, Tatenda Magodi, Rukhsar Osman, Hajaj Salum
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引用次数: 0

摘要

重症肌无力(MG)是一种引起肌肉无力的自身免疫性疾病。若在18岁前确诊,则称为少年MG。眼部症状在儿童中比成人更常见。眼部MG的诊断包括冰袋试验等检查,而治疗包括胆碱酯酶抑制剂和皮质类固醇。病例介绍:我们报告了一个3岁的女孩,她有两个月的进行性眼睑无力史,但没有其他身体无力报告。在冰袋试验阳性和检测抗乙酰胆碱受体自身抗体后,她被诊断为眼部MG。她开始使用吡哆斯的明,后来加用环孢素,之后症状明显改善。结论:眼部MG罕见。本病例报告强调了在低资源环境下诊断和管理眼部MG的挑战,强调了早期识别和治疗的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Juvenile Ocular Myasthenia Gravis in a 3-Year-Old African Girl: A Case Report.

Juvenile Ocular Myasthenia Gravis in a 3-Year-Old African Girl: A Case Report.

Juvenile Ocular Myasthenia Gravis in a 3-Year-Old African Girl: A Case Report.

Introduction: Myasthenia gravis (MG) is an autoimmune disorder causing muscle weakness. When diagnosed before 18, it is termed juvenile MG. Ocular symptoms are more common in children than adults. Diagnosis of ocular MG involves tests like the ice pack test, while treatment includes cholinesterase inhibitors and corticosteroids.

Case presentation: We present a case of a 3-year-old girl who had a 2-month history of progressive weakness of both eyelids, but no other body weakness reported. She was diagnosed with ocular MG after a positive ice pack test and detection of autoantibodies against acetylcholine receptors. She was started on pyridostigmine and later added cyclosporine, and her symptoms improved greatly afterward.

Conclusion: Ocular MG is rare. This case report highlights the challenges of diagnosing and managing ocular MG in low-resource settings, stressing the need for early recognition and treatment.

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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
129
审稿时长
12 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of ophthalmology, including prevention, diagnosis, treatment, toxicities of therapy, supportive care, quality-of-life, and survivorship issues. The submission of negative results is strongly encouraged. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed. The intent of the journal is to provide clinicians and researchers with a tool to disseminate their personal experiences to a wider public as well as to review interesting cases encountered by colleagues all over the world. Universally used terms can be searched across the entire growing collection of case reports, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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