{"title":"Myelin oligodendrocyte glycoprotein antibody-associated disease after transforaminal lumbar interbody fusion surgery: a case report.","authors":"Yicheng Qian, Yingying Shi, Yixuan Kang, Yucheng Fu, Wei Yu, Kan Xu","doi":"10.1007/s10072-026-09080-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Postoperative myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) represents a rare clinical entity that poses significant diagnostic challenges. Despite its clinical relevance, limited attention has been directed toward postoperative MOGAD, compounded by its heterogeneous symptom presentation and potential mimicry of other postoperative complications. This case study provides critical insights into the diagnostic and therapeutic management of postoperative MOGAD, emphasizing the necessity for early recognition and appropriate treatment. We present a case of a 27-year-old female who developed refractory fever following transforaminal lumbar interbody fusion (TLIF) surgery. Initial treatment focused on suspected surgical site inflammation, with empirical broad-spectrum antibiotics administered. However, progressive neurological manifestations including bilateral vision impairment, headache, and positive serum MOG-IgG prompted revision of the diagnosis to MOGAD. The patient subsequently received targeted therapy and recovered well.</p><p><strong>Results: </strong>The patient received methylprednisolone, mannitol, and intravenous immunoglobulin therapy. This regimen achieved complete neurological recovery, with resolution of visual deficits and normalization of inflammatory markers.</p><p><strong>Conclusion: </strong>This case highlights the importance of identifying postoperative MOGAD as a potential complication and underscores the need for early and accurate diagnosis. Increased awareness and prompt intervention could prevent unnecessary delays in treatment and improve patient prognosis.</p>","PeriodicalId":19191,"journal":{"name":"Neurological Sciences","volume":"47 6","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2026-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurological Sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10072-026-09080-7","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Postoperative myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) represents a rare clinical entity that poses significant diagnostic challenges. Despite its clinical relevance, limited attention has been directed toward postoperative MOGAD, compounded by its heterogeneous symptom presentation and potential mimicry of other postoperative complications. This case study provides critical insights into the diagnostic and therapeutic management of postoperative MOGAD, emphasizing the necessity for early recognition and appropriate treatment. We present a case of a 27-year-old female who developed refractory fever following transforaminal lumbar interbody fusion (TLIF) surgery. Initial treatment focused on suspected surgical site inflammation, with empirical broad-spectrum antibiotics administered. However, progressive neurological manifestations including bilateral vision impairment, headache, and positive serum MOG-IgG prompted revision of the diagnosis to MOGAD. The patient subsequently received targeted therapy and recovered well.
Results: The patient received methylprednisolone, mannitol, and intravenous immunoglobulin therapy. This regimen achieved complete neurological recovery, with resolution of visual deficits and normalization of inflammatory markers.
Conclusion: This case highlights the importance of identifying postoperative MOGAD as a potential complication and underscores the need for early and accurate diagnosis. Increased awareness and prompt intervention could prevent unnecessary delays in treatment and improve patient prognosis.
期刊介绍:
Neurological Sciences is intended to provide a medium for the communication of results and ideas in the field of neuroscience. The journal welcomes contributions in both the basic and clinical aspects of the neurosciences. The official language of the journal is English. Reports are published in the form of original articles, short communications, editorials, reviews and letters to the editor. Original articles present the results of experimental or clinical studies in the neurosciences, while short communications are succinct reports permitting the rapid publication of novel results. Original contributions may be submitted for the special sections History of Neurology, Health Care and Neurological Digressions - a forum for cultural topics related to the neurosciences. The journal also publishes correspondence book reviews, meeting reports and announcements.