Bin Abdulqader Sarah A, Alkhalidi Hisham M, Ajlan Abdulrazag M
Department of Neurosurgery, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:
Neurosciences (Riyadh). 2018 Apr;23(2):152-157. doi: 10.17712/nsj.2018.2.20170401.
Brainstem encephalitis (BE) is a rare, severe, and potentially life-threatening inflammation of the central nervous system. Brainstem encephalitis has multiple etiologies, which vary in treatment and outcomes. The current literature is generally focused on the infectious causes of BE, while little is known about the other entities, including cases with inconclusive diagnoses. Additionally, the outcomes of BE are not well documented. We present a case of an 18-year-old male who presented with progressive symptoms of brainstem involvement. His clinical investigations, including cerebrospinal fluid (CSF) analysis, were normal; magnetic resonance imaging (MRI) of the brain showed an enhancing medullary lesion, while tissue biopsy yielded no specific diagnosis. Multiple empirical treatments to address possible autoimmune and infectious processes were started with no significant improvement. He continued to deteriorate over a period of 12 weeks. Thereafter, following intensive supportive and rehabilitative care, he started to show slow signs of improvement.
脑干脑炎(BE)是一种罕见、严重且可能危及生命的中枢神经系统炎症。脑干脑炎有多种病因,其治疗方法和预后各不相同。当前的文献通常聚焦于脑干脑炎的感染性病因,而对于其他病因,包括诊断不明确的病例,人们了解甚少。此外,脑干脑炎的预后情况也缺乏充分记录。我们报告一例18岁男性病例,该患者出现了脑干受累的进行性症状。他的临床检查,包括脑脊液(CSF)分析,结果均正常;脑部磁共振成像(MRI)显示延髓有强化病变,而组织活检未得出明确诊断。针对可能的自身免疫和感染过程启动了多种经验性治疗,但均未取得显著改善。在12周的时间里,他的病情持续恶化。此后,经过强化的支持治疗和康复护理,他开始出现缓慢的改善迹象。