Atypical initial presentation of MOGAD in a patient with probable tuberculous meningoencephalitis: Case report

Neuroimmunology Reports Pub Date : 2025-01-01 Epub Date: 2024-12-22 DOI:10.1016/j.nerep.2024.100237
Diego Canales, Stefany Espinoza, Maria Burgos, Pablo Orosco
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Abstract

Tuberculosis (TB) is an endemic disease in our country that effects on various organs and at the nervous system. The diagnosis requires confirmatory tests, however if the suspicion is high, empirical treatment can be initiated with subsequent follow-up of the patient.
TB has been associated with neuromyelitis optica, however it didn't associate with MOG antibody disease (MOGAD). MOGAD is a rare entity in the adult population; its main manifestation is bilateral optic neuritis or acute disseminated encephalitis. Which also requires confirmatory tests and immunosuppressive treatment.
We report the case of a patient diagnosed with TB meningoencephalitis, in the second month of empirical treatment with anti-TB drugs, who was admitted to our service due to persistence of epileptic seizures and greater deterioration in the level of alertness. She was tested for infectious, autoimmune, tumor and metabolic diseases, which came out within the normal range. Magnetic resonance imaging showed apparently sequelae diffuse bilateral leukodystrophy without contrast enhancement. The possibility of autoimmune encephalitis was evaluated. Therefore, it decided to start treatment with immunoglobulin for 6 cycles. During her evolution, clinical improvement was evident, without epileptic seizures, with better interaction with his environment and she began to walk with a walker. At the end of the anti-TB and immunoglobulin treatment, she presented an episode of dysarthria and facial asymmetry. The new image showed nodular lesions in the midbrain and cerebellum, some of which captured contrast. Therefore, the studies were expanded and an anti-MOG test was performed, which was positive. It was decided to start immunoglobulin cycles. With apparently good clinical evolution.

Conclusion

We present the case of an atypical initial presentation of MOGAD. This should be taken into account in cases where there is no adequate clinical improvement, since treatment with corticosteroids or immunoglobulins may be effective in these patients and prevent serious sequelae.
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一例疑似结核性脑膜脑炎患者MOGAD的不典型初始表现:病例报告
结核病(TB)是我国一种影响人体各器官和神经系统的地方病。诊断需要确认性检查,但如果怀疑程度高,可通过对患者的后续随访开始经验性治疗。结核与视神经脊髓炎相关,但与MOG抗体病(MOGAD)无关。MOGAD在成年人群中是一个罕见的实体;主要表现为双侧视神经炎或急性播散性脑炎。这也需要确认性检查和免疫抑制治疗。我们报告的情况下,诊断为结核脑膜脑炎的病人,在第二个月的经验治疗抗结核药物,谁是入院我们的服务,由于持续的癫痫发作和警觉性水平更大的恶化。她接受了传染病、自身免疫性疾病、肿瘤和代谢疾病的检查,结果都在正常范围内。磁共振成像显示明显的双侧弥漫性脑白质营养不良后遗症,无增强。评估自身免疫性脑炎的可能性。因此,决定开始使用免疫球蛋白治疗6个周期。在她的发展过程中,临床改善很明显,没有癫痫发作,与环境的互动更好,她开始用助行器走路。在抗结核和免疫球蛋白治疗结束时,她出现构音障碍和面部不对称。新图像显示了中脑和小脑的结节状病变,其中一些得到了对比。因此,我们扩大了研究范围,进行了抗mog试验,结果为阳性。决定开始免疫球蛋白循环。临床进展明显良好。结论我们提出一例非典型的MOGAD的初始表现。在没有充分临床改善的情况下,应考虑到这一点,因为皮质类固醇或免疫球蛋白治疗可能对这些患者有效,并防止严重的后遗症。
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