Duggal Neeta, Ahmed Iftekhar, Duggal Nikki
University of Missouri at Kansas City
Research Medical Center
J Vasc Interv Neurol. 2014 Nov;7(4):19-22.
Acute hemorrhagic leukoencephalitis is a rare acute inflammatory myelinopathy of central nervous system with high mortality. We report a case of an unusual presentation of acute hemorrhagic leukoencephalitis with autoimmune myopathy and a complete recovery with steroids and plasmapheresis.
A 24-year-old female admitted with generalized seizure, lethargy, but no focal neurological signs. Head scans revealed right frontal hypodensity with loss of basal cisterns, mild transfalcine shift to the left, a mass lesion with abnormal signal and multiple small hemorrhages. Biopsy pathology showed white matter demyelinating lesions with necrotizing destruction of small vessels and acute inflammation. EMG was consistent with demyelinating diffuse polyneuropathy and myopathy. Pathology of muscle showed myopathic changes suggestive of autoimmune myopathy.
Patient was initially treated with Dexamethasone, Mannitol, Keppra, Antibiotics and Acyclovir. Later when she developed diffuse polyneuropathy and myopathy, she was given plasmapheresis. The patient responded to the treatment and made a full recovery.
Acute hemorrhagic leukoencephalitis is a rare and usually fatal disorder. The etiology of AHLE remains clear; cross-reactivity between human myelin antigens and viral or bacterial antigens is thought to initiate an immune process causing demyelination. Usually the autoimmune process targets CNS myelin and spares the peripheral; however, in this case there was diffuse involvement of central and peripheral myelin and muscle.
急性出血性白质脑炎是一种罕见的中枢神经系统急性炎症性脱髓鞘病,死亡率高。我们报告一例急性出血性白质脑炎合并自身免疫性肌病的不寻常表现病例,经类固醇和血浆置换治疗后完全康复。
一名24岁女性因全身性癫痫发作、嗜睡入院,但无局灶性神经体征。头部扫描显示右额叶低密度影,脑基底池消失,轻度大脑镰下疝向左移位,一个有异常信号的肿块病变和多处小出血。活检病理显示白质脱髓鞘病变,伴有小血管坏死性破坏和急性炎症。肌电图与脱髓鞘性弥漫性多发性神经病和肌病一致。肌肉病理显示肌病性改变,提示自身免疫性肌病。
患者最初接受地塞米松、甘露醇、开浦兰、抗生素和阿昔洛韦治疗。后来当她出现弥漫性多发性神经病和肌病时,接受了血浆置换治疗。患者对治疗有反应并完全康复。
急性出血性白质脑炎是一种罕见且通常致命的疾病。急性出血性白质脑炎的病因尚不清楚;人类髓鞘抗原与病毒或细菌抗原之间的交叉反应被认为引发了导致脱髓鞘的免疫过程。通常自身免疫过程以中枢神经系统髓鞘为靶点,不累及外周;然而,在本病例中,中枢和外周髓鞘及肌肉均有弥漫性受累。