被误诊为特发性双侧感音神经性聋的表层铁沉积症
Superficial siderosis misdiagnosed as idiopathic bilateral neurosensorial deafness.
作者信息
González-Usigli H A, Perez-Torres Teresa, Saenz-Farret Michel, Rivero-Moragrega Paloma
机构信息
Department of Neurology, Instituto Mexicano del Seguro Social Delegacion Jalisco, Guadalajara, Mexico.
Department of Neurology, Hospital de Especialidades del Centro Medico Nacional de Occidente IMSS, Guadalajara, Mexico.
出版信息
BMJ Case Rep. 2018 Jul 11;2018:bcr-2017-222639. doi: 10.1136/bcr-2017-222639.
Abstract
Superficial siderosis (SS) is a rare condition resulting from different sources of bleeding into the subpial space. The most common symptoms are: hypoacusia, ataxia, incontinence, dementia and parkinsonism. Since several neurodegenerative disorders may present with same clinical features, SS is often misdiagnosed. Here we present a case of SS misdiagnosed as idiopathic bilateral neurosensorial deafness.
摘要
浅表性铁沉积症（SS）是一种罕见的疾病，由不同来源的血液渗入软脑膜下间隙引起。最常见的症状包括：听力减退、共济失调、失禁、痴呆和帕金森综合征。由于几种神经退行性疾病可能具有相同的临床特征，SS常常被误诊。在此，我们报告一例被误诊为特发性双侧神经性耳聋的SS病例。
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