Stavrou Maria, Francis Lucy, Tshuma Nomathamsanqa, Schmierer Klaus
Centre of Clinical Brain Sciences, University of Edinburgh, Edinburgh.
Clinical Board: Medicine (Neuroscience), The Royal London Hospital, Barts Health NHS Trust, London, United Kingdom.
BMJ Case Rep. 2018 May 23;2018:bcr-2017-222255. doi: 10.1136/bcr-2017-222255.
Rhomboencephalitis, at least in its acute phase, is often a severely disabling syndrome, and can be life threatening. A range of underlying conditions can lead to this clinical syndrome. Rapid diagnosis to initiate treatment early is key to a beneficial outcome. We report the case of a 22 year old Afro-Caribbean woman, who presented with a two -week history of walking difficulties, upper limb incoordination and slurred speech. Her brainstem function deteriorated at pace, and she developed hypersomnia. A broad diagnostic approach led to prophylactic treatment for the most common infectious causes. This did not improve her symptoms. Non-infectious inflammatory causes were therefore considered and plasma exchange treatment was initiated leading to marked improvement within days. Screening for autoimmune conditions confirmed aquaporin-4 positive neuromyelitis optica spectrum disorder (NMOSD) as the underlying cause. Immunotherapy with rituximab was started. So far, no relapse has been observed. While the definition of NMOSD continues to be refined, aquaporin-4 testing should be considered early in patients presenting with rhomboencephalitis who do not respond to antibiotic and antiviral treatment. Vigilance and early intervention are key to limit morbidity and mortality from NMOSD.
菱形脑炎,至少在急性期,通常是一种严重致残的综合征,甚至可能危及生命。一系列潜在疾病都可能导致这种临床综合征。早期快速诊断以启动治疗是取得良好预后的关键。我们报告一例22岁的非洲加勒比裔女性病例,她有两周的行走困难、上肢共济失调和言语含糊不清病史。她的脑干功能迅速恶化,并出现了嗜睡症状。广泛的诊断方法导致针对最常见感染原因进行了预防性治疗。但这并未改善她的症状。因此考虑了非感染性炎症原因,并开始进行血浆置换治疗,数天内症状明显改善。自身免疫性疾病筛查确诊水通道蛋白4阳性视神经脊髓炎谱系障碍(NMOSD)为根本病因。开始使用利妥昔单抗进行免疫治疗。到目前为止,尚未观察到复发情况。虽然NMOSD的定义仍在不断完善,但对于患有菱形脑炎且对抗生素和抗病毒治疗无反应的患者,应尽早考虑进行水通道蛋白4检测。警惕和早期干预是限制NMOSD发病率和死亡率的关键。