Morotti Andrea, Liberini Paolo, Padovani Alessandro
Neurology Unit, University of Brescia, Italy.
BMJ Case Rep. 2013 Jan 29;2013:bcr2011007959. doi: 10.1136/bcr-2012-007959.
Optic perineuritis (OPN) is an uncommon inflammatory disorder of the optic nerve sheath. Most cases are idiopathic, though OPN can rarely occur as a manifestation of vasculitic diseases. We describe the case of a 74-year-old Caucasian man presenting with diplopia and bilateral visual loss. A brain MRI showed bilateral OPN without involvement of other structures. All the tests performed to investigate OPN's aetiology showed negative results. Considering clinical presentation and neuroimaging findings, a diagnosis of bilateral idiopathic OPN was made. Treatment with intravenous high-dose steroid was administered. Four weeks after admission, the steroid therapy was interrupted because of Listeria monocytogenes invasive infection. After steroid treatment withdrawal, the patient developed jaw claudication and bilateral skin necrosis of the temporal region, clinical features that are highly specific for giant cell arteritis (GCA). On this basis, a diagnosis of bilateral OPN secondary to GCA was made.
视神经周围炎(OPN)是一种罕见的视神经鞘炎性疾病。大多数病例为特发性,不过OPN很少作为血管炎性疾病的一种表现出现。我们描述了一名74岁白种男性患者,其表现为复视和双侧视力丧失。脑部磁共振成像(MRI)显示双侧OPN,未累及其他结构。为探究OPN病因所进行的所有检查结果均为阴性。综合临床表现和神经影像学检查结果,诊断为双侧特发性OPN。给予静脉注射大剂量类固醇治疗。入院四周后,因单核细胞增生李斯特菌侵袭性感染中断类固醇治疗。停用类固醇治疗后,患者出现颌部间歇性运动障碍和颞部双侧皮肤坏死,这些临床特征是巨细胞动脉炎(GCA)的高度特异性表现。基于此,诊断为继发于GCA的双侧OPN。