MOGAD在MRI上的强化特点
MRI Enhancement Features in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)
DOI: 10.12677/acm.2026.162370, PDF,   
作者: 张 鹭, 冯 川*:重庆医科大学附属儿童医院放射科,儿童发育疾病研究教育部重点实验室,儿童发育重大疾病国家国际科技合作基地,儿童代谢与炎症性疾病重庆市重点实验室,重庆
关键词: MOG抗体相关性疾病增强视神经炎脊髓炎脑炎MOG Antibody-Associated Disease (MOGAD) Enhancement Optic Neuritis Myelitis Encephalitis
摘要: MOG抗体相关性疾病(MOGAD)是一种以抗髓鞘少突胶质细胞糖蛋白抗体为特征的自身免疫性中枢神经系统脱髓鞘疾病,其临床表型主要包括视神经炎、脊髓炎和脑炎。MRI增强是诊断与评估MOGAD的重要工具,强化特征可反映活动性炎症与血脑屏障破坏,并可能与疾病预后相关。本文总结了MOGAD在MRI上的强化表现:视神经炎常表现为双侧视神经广泛强化,伴视神经鞘及周围眶内组织强化(神经周围增强),具有较高特异性;脊髓炎多见于长节段横贯性脊髓炎,轴位可见中央型T2高信号或“H征”,部分伴有软脑膜或脊神经根强化;脑炎强化形式多样,多为斑片状、结节状或线样强化,软脑膜强化亦较常见,而环形强化少见。这些强化特征有助于MOGAD与多发性硬化、水通道蛋白-4抗体相关视神经脊髓炎谱系疾病等相鉴别。准确识别MOGAD的MRI强化模式对于早期诊断、指导治疗及判断预后具有重要意义。
Abstract: Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease (MOGAD) is an autoimmune demyelinating disorder of the central nervous system characterized by antibodies against myelin oligodendrocyte glycoprotein. Its clinical manifestations primarily include optic neuritis, myelitis, and encephalitis. Contrast-enhanced Magnetic Resonance Imaging (MRI) serves as a key tool for diagnosis and evaluation of MOGAD, with enhancement features reflecting active inflammation and blood-brain barrier disruption, which may correlate with disease prognosis. This review summarizes the enhancement patterns of MOGAD on MRI: optic neuritis typically presents with bilateral longitudinally extensive optic nerve enhancement, often accompanied by perineural enhancement involving the optic nerve sheath and surrounding orbital tissues, showing high diagnostic specificity; myelitis commonly manifests as longitudinally extensive transverse myelitis with central T2-hyperintensity on axial images, sometimes exhibiting an “H-sign”, and may be associated with leptomeningeal or spinal nerve root enhancement; encephalitis demonstrates diverse enhancement patterns, including patchy, nodular, or linear enhancement, with leptomeningeal enhancement also frequently observed, whereas ring enhancement is rare. These enhancement characteristics help distinguish MOGAD from multiple sclerosis, aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder, and other demyelinating diseases. Accurate recognition of MRI enhancement patterns in MOGAD is crucial for early diagnosis, guiding treatment decisions, and predicting clinical outcomes.
文章引用:张鹭, 冯川. MOGAD在MRI上的强化特点[J]. 临床医学进展, 2026, 16(2): 131-138. https://doi.org/10.12677/acm.2026.162370

参考文献

[1] Narayan, R., Simpson, A., Fritsche, K., Salama, S., Pardo, S., Mealy, M., et al. (2018) MOG Antibody Disease: A Review of MOG Antibody Seropositive Neuromyelitis Optica Spectrum Disorder. Multiple Sclerosis and Related Disorders, 25, 66-72. [Google Scholar] [CrossRef] [PubMed]
[2] de Mol, C., Wong, Y., van Pelt, E., Wokke, B., Siepman, T., Neuteboom, R., et al. (2019) The Clinical Spectrum and Incidence of Anti-MOG-Associated Acquired Demyelinating Syndromes in Children and Adults. Multiple Sclerosis Journal, 26, 806-814. [Google Scholar] [CrossRef] [PubMed]
[3] O’Connell, K., Hamilton-Shield, A., Woodhall, M., Messina, S., Mariano, R., Waters, P., et al. (2020) Prevalence and Incidence of Neuromyelitis Optica Spectrum Disorder, Aquaporin-4 Antibody-Positive NMOSD and MOG Antibody-Positive Disease in Oxfordshire, Uk. Journal of Neurology, Neurosurgery & Psychiatry, 91, 1126-1128. [Google Scholar] [CrossRef] [PubMed]
[4] Bruijstens, A.L., Lechner, C., Flet-Berliac, L., Deiva, K., Neuteboom, R.F., Hemingway, C., et al. (2020) E.U. Paediatric MOG Consortium Consensus: Part 1—Classification of Clinical Phenotypes of Paediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disorders. European Journal of Paediatric Neurology, 29, 2-13. [Google Scholar] [CrossRef] [PubMed]
[5] Banwell, B., Bennett, J.L., Marignier, R., Kim, H.J., Brilot, F., Flanagan, E.P., et al. (2023) Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease: International MOGAD Panel Proposed Criteria. The Lancet Neurology, 22, 268-282. [Google Scholar] [CrossRef] [PubMed]
[6] Corbali, O. and Chitnis, T. (2023) Pathophysiology of Myelin Oligodendrocyte Glycoprotein Antibody Disease. Frontiers in Neurology, 14, Article 1137998. [Google Scholar] [CrossRef] [PubMed]
[7] Fan, X., Li, Q., Li, T., He, X., Feng, C., Qin, B., et al. (2022) Radiological Features for Outcomes of MOGAD in Children: A Cohort in Southwest China. Neuropsychiatric Disease and Treatment, 18, 1875-1884. [Google Scholar] [CrossRef] [PubMed]
[8] Waters, P., Fadda, G., Woodhall, M., O’Mahony, J., Brown, R.A., Castro, D.A., et al. (2020) Serial Anti-Myelin Oligodendrocyte Glycoprotein Antibody Analyses and Outcomes in Children with Demyelinating Syndromes. JAMA Neurology, 77, 82-93. [Google Scholar] [CrossRef] [PubMed]
[9] Cobo-Calvo, A., Ruiz, A., Rollot, F., Arrambide, G., Deschamps, R., Maillart, E., et al. (2020) Clinical Features and Risk of Relapse in Children and Adults with Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease. Annals of Neurology, 89, 30-41. [Google Scholar] [CrossRef] [PubMed]
[10] Bennett, J.L., Costello, F., Chen, J.J., Petzold, A., Biousse, V., Newman, N.J., et al. (2023) Optic Neuritis and Autoimmune Optic Neuropathies: Advances in Diagnosis and Treatment. The Lancet Neurology, 22, 89-100. [Google Scholar] [CrossRef] [PubMed]
[11] Ramanathan, S., Prelog, K., Barnes, E.H., Tantsis, E.M., Reddel, S.W., Henderson, A.P., et al. (2015) Radiological Differentiation of Optic Neuritis with Myelin Oligodendrocyte Glycoprotein Antibodies, Aquaporin-4 Antibodies, and Multiple Sclerosis. Multiple Sclerosis Journal, 22, 470-482. [Google Scholar] [CrossRef] [PubMed]
[12] Chen, J.J. and Bhatti, M.T. (2020) Clinical Phenotype, Radiological Features, and Treatment of Myelin Oligodendrocyte Glycoprotein-Immunoglobulin G (MOG-IgG) Optic Neuritis. Current Opinion in Neurology, 33, 47-54. [Google Scholar] [CrossRef] [PubMed]
[13] Sechi, E., Cacciaguerra, L., Chen, J.J., Mariotto, S., Fadda, G., Dinoto, A., et al. (2022) Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): A Review of Clinical and MRI Features, Diagnosis, and Management. Frontiers in Neurology, 13, Article 885218. [Google Scholar] [CrossRef] [PubMed]
[14] Chen, J.J., Flanagan, E.P., Jitprapaikulsan, J., López-Chiriboga, A.S., Fryer, J.P., Leavitt, J.A., et al. (2018) Myelin Oligodendrocyte Glycoprotein Antibody-Positive Optic Neuritis: Clinical Characteristics, Radiologic Clues, and Outcome. American Journal of Ophthalmology, 195, 8-15. [Google Scholar] [CrossRef] [PubMed]
[15] Winter, A. and Chwalisz, B. (2020) MRI Characteristics of NMO, MOG and MS Related Optic Neuritis. Seminars in Ophthalmology, 35, 333-342. [Google Scholar] [CrossRef] [PubMed]
[16] Jiang, S., Dong, H., Yan, L., et al. (2017) Go-Sha-Jinki-Gan (GJG) Palliates Inflammation in Experimental Autoimmune Encephalomyelitis (EAE) Mice. Journal of the Neurological Sciences, 381, 174-179.
[17] Mariano, R., Messina, S., Kumar, K., Kuker, W., Leite, M.I. and Palace, J. (2019) Comparison of Clinical Outcomes of Transverse Myelitis among Adults with Myelin Oligodendrocyte Glycoprotein Antibody vs Aquaporin-4 Antibody Disease. JAMA Network Open, 2, e1912732. [Google Scholar] [CrossRef] [PubMed]
[18] Dubey, D., Pittock, S.J., Krecke, K.N., Morris, P.P., Sechi, E., Zalewski, N.L., et al. (2019) Clinical, Radiologic, and Prognostic Features of Myelitis Associated with Myelin Oligodendrocyte Glycoprotein Autoantibody. JAMA Neurology, 76, 301-309. [Google Scholar] [CrossRef] [PubMed]
[19] Zhangbao, J., Huang, W., Zhou, L., Wang, L., Chang, X., Lu, C., et al. (2020) Myelitis in Inflammatory Disorders Associated with Myelin Oligodendrocyte Glycoprotein Antibody and Aquaporin-4 Antibody: A Comparative Study in Chinese Han Patients. European Journal of Neurology, 28, 1308-1315. [Google Scholar] [CrossRef] [PubMed]
[20] Kim, H.J., Paul, F., Lana-Peixoto, M.A., Tenembaum, S., Asgari, N., Palace, J., et al. (2015) MRI Characteristics of Neuromyelitis Optica Spectrum Disorder: An International Update. Neurology, 84, 1165-1173. [Google Scholar] [CrossRef] [PubMed]
[21] Salama, S., Khan, M., Shanechi, A., Levy, M. and Izbudak, I. (2020) MRI Differences between MOG Antibody Disease and AQP4 NMOSD. Multiple Sclerosis Journal, 26, 1854-1865. [Google Scholar] [CrossRef] [PubMed]
[22] Ren, C., Zhang, W., Zhou, A., Zhou, J., Cheng, H., Tang, X., et al. (2023) Clinical and Radiologic Features among Children with Myelin Oligodendrocyte Glycoprotein Antibody-Associated Myelitis. Pediatric Neurology, 143, 96-99. [Google Scholar] [CrossRef] [PubMed]
[23] El Naggar, I., Cleaveland, R., Wendel, E., Bertolini, A., Schanda, K., Karenfort, M., et al. (2022) MR Imaging in Children with Transverse Myelitis and Acquired Demyelinating Syndromes. Multiple Sclerosis and Related Disorders, 67, Article ID: 104068. [Google Scholar] [CrossRef] [PubMed]
[24] Rinaldi, S., Davies, A., Fehmi, J., Beadnall, H.N., Wang, J., Hardy, T.A., et al. (2021) Overlapping Central and Peripheral Nervous System Syndromes in MOG Antibody-Associated Disorders. Neurology Neuroimmunology & Neuroinflammation, 8, e943. [Google Scholar] [CrossRef] [PubMed]
[25] Fadda, G., Alves, C.A., O’Mahony, J., Castro, D.A., Yeh, E.A., Marrie, R.A., et al. (2021) Comparison of Spinal Cord Magnetic Resonance Imaging Features among Children with Acquired Demyelinating Syndromes. JAMA Network Open, 4, e2128871. [Google Scholar] [CrossRef] [PubMed]
[26] Pagany, M., Jagodic, M., Schubart, A., Pham-Dinh, D., Bachelin, C., Baron van Evercooren, A., et al. (2003) Myelin Oligodendrocyte Glycoprotein Is Expressed in the Peripheral Nervous System of Rodents and Primates. Neuroscience Letters, 350, 165-168. [Google Scholar] [CrossRef] [PubMed]
[27] Sundaram, S., Nair, S.S., Jaganmohan, D., Unnikrishnan, G. and Nair, M. (2019) Relapsing Lumbosacral Myeloradiculitis: An Unusual Presentation of MOG Antibody Disease. Multiple Sclerosis Journal, 26, 509-511. [Google Scholar] [CrossRef] [PubMed]
[28] Reindl, M. and Waters, P. (2018) Myelin Oligodendrocyte Glycoprotein Antibodies in Neurological Disease. Nature Reviews Neurology, 15, 89-102. [Google Scholar] [CrossRef] [PubMed]
[29] Armangue, T., Olivé-Cirera, G., Martínez-Hernandez, E., Sepulveda, M., Ruiz-Garcia, R., Muñoz-Batista, M., et al. (2020) Associations of Paediatric Demyelinating and Encephalitic Syndromes with Myelin Oligodendrocyte Glycoprotein Antibodies: A Multicentre Observational Study. The Lancet Neurology, 19, 234-246. [Google Scholar] [CrossRef] [PubMed]
[30] Li, H., Yang, L., Wu, Z., Zhou, L., Bao, Y., Geng, D., et al. (2020) Brain MRI Features of Chinese Han Patients with MOG-Antibody Disease. Multiple Sclerosis and Related Disorders, 43, Article ID: 102167. [Google Scholar] [CrossRef] [PubMed]
[31] Banks, S.A., Morris, P.P., Chen, J.J., et al. (2020) Brainstem and Cerebellar Involvement in MOG-IgG-Associated Disorder versus Aquaporin-4-IgG and MS. Journal of Neurology, Neurosurgery & Psychiatry, 91, 1092-1094.
[32] Habib, A.A., Marton, L.S., Allwardt, B., Gulcher, J.R., Mikol, D.D., Högnason, T., et al. (1998) Expression of the Oligodendrocyte-Myelin Glycoprotein by Neurons in the Mouse Central Nervous System. Journal of Neurochemistry, 70, 1704-1711. [Google Scholar] [CrossRef] [PubMed]
[33] Hochmeister, S., Gattringer, T., Asslaber, M., Stangl, V., Haindl, M.T., Enzinger, C., et al. (2020) A Fulminant Case of Demyelinating Encephalitis with Extensive Cortical Involvement Associated with Anti-MOG Antibodies. Frontiers in Neurology, 11, Article 31. [Google Scholar] [CrossRef] [PubMed]
[34] Elsbernd, P., Cacciaguerra, L., Krecke, K.N., Chen, J.J., Gritsch, D., Lopez-Chiriboga, A.S., et al. (2023) Cerebral Enhancement in MOG Antibody-Associated Disease. Journal of Neurology, Neurosurgery & Psychiatry, 95, 14-18. [Google Scholar] [CrossRef] [PubMed]
[35] Cobo-Calvo, A., Ayrignac, X., Kerschen, P., Horellou, P., Cotton, F., Labauge, P., et al. (2019) Cranial Nerve Involvement in Patients with MOG Antibody-Associated Disease. Neurology Neuroimmunology & Neuroinflammation, 6, e543. [Google Scholar] [CrossRef] [PubMed]
[36] He, J., Grossman, R.I., Ge, Y., et al. (2001) Enhancing Patterns in Multiple Sclerosis: Evolution and Persistence. American Journal of Neuroradiology, 22, 664-669.
[37] Taieb, G., Duran-Peña, A., de Chamfleur, N.M., Moulignier, A., Thouvenot, E., Allou, T., et al. (2015) Punctate and Curvilinear Gadolinium Enhancing Lesions in the Brain: A Practical Approach. Neuroradiology, 58, 221-235. [Google Scholar] [CrossRef] [PubMed]
[38] Zhang, L., Feng, C., He, L., Huang, S., Liu, X. and Fan, X. (2024) MOG-Antibody-Associated Transverse Myelitis with the H-Sign and Unusual MRI Enhancement: A Case Report and Literature Review. Frontiers in Pediatrics, 12, Article 1451688. [Google Scholar] [CrossRef] [PubMed]