A patient with neuronal intranuclear inclusion disease developed encephalitis‐like symptoms after cerebral angiography

IF 0.4 Q4 CLINICAL NEUROLOGY Neurology and Clinical Neuroscience Pub Date : 2024-06-14 DOI:10.1111/ncn3.12839
Shingo Koide, Shintaro Tsuboguchi, Shingo Koide, Itaru Ninomiya, Taiki Saito, T. Ishiguro, E. Saji, Yo Higuchi, Takeshi Ikeuchi, Makoto Oishi, Masato Kanazawa, Osamu Onodera
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Abstract

Patients with neuronal intranuclear inclusion disease (NIID) can present with encephalitis‐like symptoms such as recurrent paroxysmal fever and unconsciousness. To date, no specific triggers for these symptoms have been reported. In our case, an 78‐year‐old woman became unconscious and developed fever after cerebral angiography. The patient had experienced four episodes of unconsciousness and fever in the past 7 years. Postangiography, she immediately became unconscious and developed fever. No vascular abnormalities were found and magnetic resonance imaging of the brain revealed expanding white matter lesions and hyperintense lesions along the corticomedullary junction. Genetic analysis revealed an abnormal GGC repeat expansion in NOTCH2NLC. Thus, we diagnosed the patient with NIID. We suggest that cerebral angiography is a possible trigger for encephalitis‐like symptoms in NIID.
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一名神经元核内包涵体病患者在脑血管造影术后出现脑炎样症状
神经元核内包涵体病(NIID)患者会出现类似脑炎的症状,如反复阵发性发热和昏迷。迄今为止,还没有关于这些症状具体诱因的报道。在我们的病例中,一名 78 岁的妇女在脑血管造影术后出现昏迷和发热。该患者在过去 7 年中曾经历过 4 次昏迷和发烧。做完血管造影术后,她立即昏迷并发烧。没有发现血管异常,脑磁共振成像显示白质病变扩大,皮质髓质交界处出现高密度病变。基因分析显示,NOTCH2NLC 的 GGC 重复扩展异常。因此,我们诊断该患者患有 NIID。我们认为,脑血管造影可能是 NIID 出现脑炎样症状的诱因。
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