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髓鞘少突胶质细胞糖蛋白抗体相关疾病合并硬脑膜炎:一例报告

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Complicated by Pachymeningitis: A Case Report.

作者信息

Khaladkar Sanjay M, KirdatPatil Prajakta P, Dhande Aryaman, Jhala Neeha A

机构信息

Radiodiagnosis, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, IND.

出版信息

Cureus. 2024 Jul 18;16(7):e64868. doi: 10.7759/cureus.64868. eCollection 2024 Jul.

Abstract

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a rare autoimmune disorder that primarily affects the central nervous system (CNS). We present a unique case of MOGAD complicated by pachymeningitis, which is characterized by inflammation of the dura mater. The clinical presentation included vertigo, nausea, and vomiting. A diagnostic workup confirmed MOGAD complicated by pachymeningitis. This case underscores the diverse clinical manifestations of MOGAD and highlights the challenges in diagnosis and management, particularly when complicated by rare manifestations like pachymeningitis.

摘要

髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)是一种罕见的自身免疫性疾病,主要影响中枢神经系统(CNS)。我们报告了一例罕见的MOGAD合并硬脑膜炎的病例,其特征为硬脑膜炎症。临床表现包括眩晕、恶心和呕吐。诊断检查证实为MOGAD合并硬脑膜炎。该病例强调了MOGAD的多种临床表现,并突出了诊断和管理方面的挑战,尤其是当合并像硬脑膜炎这样的罕见表现时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b197/11330373/7dd513dcbf14/cureus-0016-00000064868-i01.jpg

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