Department of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University, 600# Tianhe Road, Guangzhou, 510630, Guangdong Province, China.
Department of Neurology, Shantou Central Hospital, 114# Waima Road, Shantou, 515031, Guangdong Province, China.
J Neurol. 2024 Oct;271(10):6811-6821. doi: 10.1007/s00415-024-12633-5. Epub 2024 Aug 27.
The overlapping syndrome of anti-GFAP and anti-MOG antibodies is extremely rare. This retrospective study reports 8 adult cases of the GFAP-MOG overlapping syndrome.
We reviewed the clinical characteristics of 8 adult patients with the GFAP-MOG overlapping syndrome from Jan 2019 and Sep 2023 at the Third Affiliated Hospital, Sun Yat-sen University. Moreover, we searched the literature and included all case reports with this overlapping syndrome since 2018 on PubMed.
The predominant clinical syndrome was meningoencephalomyelitis (5/8), followed by meningoencephalitis (2/8), and myelitis (1/8). Five patients had a flu-like prodromal symptom or diarrhea. No neoplasms were found in these patients. Regarding brain MRI, T2-weighted/fluid-attenuated inversion recovery hyperintensities were in 7 patients and leptomeningeal enhancement was in 4 patients. However, only one patient had periventricular radial linear enhancement. Besides, two patients had large space-occupying lesions. For spinal MRI, T2-hyperintensities were observed in 4 patients, in which 3 patients had longitudinally extensive lesions. All patients were treated with immunotherapy, the median follow-up period was 18 months (range, 3-36 months). Three patients presented relapses during the follow-up, but all cases recovered to mRS scores ≤ 2 at last follow-up. In addition, we also reviewed 14 cases (including 7 adults and 7 children) with this overlapping syndrome by literature review.
Our findings provide data to understand the clinical features and prognosis of the GFAP-MOG overlapping syndrome. Recognizing this overlapping syndrome will expand our knowledge, allowing for better management of these patients.
抗 GFAP 和抗 MOG 抗体重叠综合征极为罕见。本回顾性研究报告了 8 例成人 GFAP-MOG 重叠综合征病例。
我们回顾了 2019 年 1 月至 2023 年 9 月中山大学附属第三医院 8 例成人 GFAP-MOG 重叠综合征患者的临床特征。此外,我们在 PubMed 上搜索了自 2018 年以来所有具有这种重叠综合征的病例报告,并将其纳入。
主要临床综合征为脑脊髓炎(5/8),其次为脑脊髓炎(2/8)和脊髓炎(1/8)。5 例患者有流感样前驱症状或腹泻。这些患者均未发现肿瘤。这些患者的脑部 MRI 显示 T2 加权/液体衰减反转恢复高信号 7 例,软脑膜增强 4 例。然而,只有 1 例患者出现脑室周围放射状线性增强。此外,2 例患者有大的占位性病变。脊髓 MRI 显示 T2 高信号 4 例,其中 3 例有纵向广泛病变。所有患者均接受免疫治疗,中位随访时间为 18 个月(范围 3-36 个月)。在随访期间,3 例患者复发,但所有病例最终随访时 mRS 评分均≤2。此外,我们还通过文献回顾,共纳入了 14 例(包括 7 例成人和 7 例儿童)这种重叠综合征的病例。
我们的研究结果为了解 GFAP-MOG 重叠综合征的临床特征和预后提供了数据。认识到这种重叠综合征将扩展我们的知识,从而更好地管理这些患者。