Evaluating the diagnosis and treatment of neuro-Behçet’s disease with cascade sign appearance in brainstem: a case report

Samaneh Hosseini, Alireza Khabazi, Mehran Ghaffari, Seyed Hossein Aghamiri
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Abstract

This study aimed to investigate a case of neuro-Behçet’s disease misdiagnosed as acute ischemic stroke or multiple sclerosis (MS). The studied case was a 29-year-old man with subacute onset of hemiparesis, dysarthria, and ataxia who was diagnosed as acute ischemic stroke at first. Due to no significant improvement, the patient was managed as an MS case, but he did not experience any improvements again. We noticed a history of oral and genital aphthous and cascade sign appearance in his brain MRI. Then, Behçet’s disease with secondary parenchymal involvement of brainstem was confirmed. The patient received infliximab, which resulted in clinico-radiological recovery. Practical Implications. Given the prevalence of Behçet’s disease in the Middle East, the possibility of its diagnosis should be considered in patients with atypical history or imaging for ischemic stroke or MS.
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脑干级联征神经病的诊断与治疗评价1例
本研究旨在探讨一例被误诊为急性缺血性脑卒中或多发性硬化症(MS)的神经behaperet病。研究的病例是一名29岁男性,患有亚急性起病偏瘫、构音障碍和共济失调,最初被诊断为急性缺血性中风。由于没有明显的改善,患者被当作MS病例处理,但他没有再次经历任何改善。我们发现他有口腔和生殖器口疮病史,脑部MRI显示有级联征。确认为继发性脑实质累及脑干的behaperet病。患者接受英夫利昔单抗治疗后,临床放射学恢复。实际意义。鉴于behet病在中东地区的流行,在有非典型病史或缺血性卒中或多发性硬化症影像的患者中,应考虑其诊断的可能性。
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