Hamed L M, Silbiger J, Guy J, Mickle J P, Sibony P, Cossari A, Andriola M
Department of Ophthalmology, University of Florida, College of Medicine, Gainesville 32610-0284.
J Clin Neuroophthalmol. 1993 Mar;13(1):18-23.
Two children developed mental status alteration and bilateral profound visual loss secondary to optic neuritis. The clinical picture was consistent with parainfectious encephalomyelitis. Magnetic resonance imaging showed bilateral involvement of the thalamus in both cases. In one case the thalamic involvement was solitary and was suspected initially to represent a primary thalamic neoplasm. This was ruled out by a stereotactic biopsy of the thalamus, which showed perivascular inflammation consistent with parainfectious encephalomyelitis. The clinical and neuroimaging findings improved significantly following corticosteroid administration. Several relapses occurred upon initial attempts at corticosteroid cessation.
两名儿童因视神经炎出现精神状态改变和双侧严重视力丧失。临床表现与感染后自身免疫性脑脊髓炎相符。磁共振成像显示两例均为双侧丘脑受累。其中一例丘脑受累为孤立性,最初怀疑是原发性丘脑肿瘤。丘脑立体定向活检排除了这种可能性,活检显示血管周围炎症与感染后自身免疫性脑脊髓炎一致。给予皮质类固醇治疗后,临床和神经影像学表现显著改善。最初尝试停用皮质类固醇时出现了几次复发。