Najjar Abdallah A, Abu Mayaleh Mahmoud A, Halaykh Roaa M, Amleh Majd Y, Atawnah Saeed I
Hebron University, Hebron, Palestine.
Department of Internal Medicine, Al Ahli Hospital, Hebron, Palestine.
Medicine (Baltimore). 2025 May 16;104(20):e42458. doi: 10.1097/MD.0000000000042458.
Acute disseminated encephalomyelitis (ADEM) is an immune-mediated demyelinating disorder of the central nervous system, often triggered by infection or vaccination. It is rare in adults and can mimic other conditions, including complex migraine, leading to potential misdiagnosis and delayed treatment.
A 35-year-old male presented with a progressive course of headache, visual disturbances, and altered mental status after an initial diagnosis of migraine.
Initial imaging was nonspecific; however, repeat magnetic resonance imaging showed multifocal high T2-weighted fluid-attenuated inversion recovery signal intensities. Cerebrospinal fluid analysis revealed elevated protein and lymphocytic pleocytosis. Infectious and autoimmune causes were excluded, supporting a diagnosis of ADEM.
The patient was treated with high-dose intravenous methylprednisolone followed by a tapering course of oral corticosteroids. Supportive therapy included antipsychotics and anticonvulsants.
Substantial clinical improvement was noted, including restoration of orientation and motor function. At the 2-week follow-up, the patient remained neurologically stable.
This case emphasizes the importance of considering ADEM in adults with atypical migraine presentations. Early recognition and corticosteroid therapy can lead to favorable outcomes.
急性播散性脑脊髓炎(ADEM)是一种中枢神经系统的免疫介导性脱髓鞘疾病,常由感染或疫苗接种引发。在成人中较为罕见,且可模仿其他病症,包括复杂性偏头痛,从而导致潜在的误诊和治疗延误。
一名35岁男性在最初被诊断为偏头痛后,出现了头痛、视觉障碍和精神状态改变的进行性病程。
初始影像学检查无特异性;然而,重复磁共振成像显示多灶性高T2加权液体衰减反转恢复信号强度。脑脊液分析显示蛋白升高和淋巴细胞增多。排除了感染和自身免疫性病因,支持ADEM的诊断。
患者接受了大剂量静脉注射甲基强的松龙治疗,随后逐渐减量口服皮质类固醇。支持性治疗包括使用抗精神病药物和抗惊厥药物。
观察到显著的临床改善,包括定向力和运动功能的恢复。在2周的随访中,患者神经功能保持稳定。
该病例强调了在具有非典型偏头痛表现的成人中考虑ADEM的重要性。早期识别和皮质类固醇治疗可带来良好的结果。