Gradenigo’s Syndrome: A Case Report

S. A. Dhali, H. Rahman, Md. Rafiqul Islam
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Abstract

The syndrome of constant otorrhea, headache, diplopia and rarely ipsilateral Horner’s syndrome, which is attributed to inflammation of the petrous apex, is known as Gradenigo’s syndrome. We report a case of Gradenigo’s syndrome, which was 50 yrs old man who presented with 6 months history of left-sided headache, facial pain, diplopia and dropping of left eyelid. Examination demonstrated a left eye lateral gaze palsy, diplopia, and dropping of left eyelid, otoscopy revealed a congested left tympanic membrane. X-ray mastoid Townes view shows mastoid air cell are reduced on left side. CT scan study confirmed mastoid air cell are reduced and scleroses on left side and MRI shows T1 hypo & T2 & FLAIR hyperintense areas are on left mastoid region which consistent with Gradenigo’s Syndrome. Bangladesh Journal of Neuroscience 2014; Vol. 30 (2): 117-119     
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格雷迪尼戈综合征1例报告
经常耳漏,头痛,复视和罕见的同侧霍纳综合征,这是由于岩尖的炎症,被称为格雷迪尼戈综合征。我们报告一位50岁男性患者,以6个月的左侧头痛、面部疼痛、复视和左眼睑下垂为主要表现。检查显示左眼侧视麻痹,复视,左眼睑下垂,耳镜检查显示左鼓膜充血。乳突x线汤斯图显示左侧乳突空气细胞缩小。CT扫描证实左侧乳突空气细胞缩小、硬化,MRI显示左侧乳突区T1低、T2高、FLAIR高,符合格雷迪尼戈综合征。孟加拉国神经科学杂志2014;Vol. 30 (2): 117-119
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