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视交叉海绵状血管瘤:单侧视力丧失的罕见原因
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作者 milea d. Karachi C. +1 位作者 Bonneville F. 韩静 《世界核心医学期刊文摘(眼科学分册)》 2005年第10期10-11,共2页
Introduction. Optic pathways cavernomas are rare vascular hamartomas that can present either with an acute chiasmai syndrome or slowly progressive visual loss . Observation. A 29-year-old patient presented with mild u... Introduction. Optic pathways cavernomas are rare vascular hamartomas that can present either with an acute chiasmai syndrome or slowly progressive visual loss . Observation. A 29-year-old patient presented with mild unilateral visual los s of rapid onset and monocular left temporal hemianopia. MRI disclosed a heterog enous enhancing optochiasmal lesion. Work-up found no evidence for an inflammat ory, infectious or tumoral disease and therefore a neurosurgical approach of the lesion allowed diagnosis of cavernoma, confirmed by pathological examination. S uccessful resection resulted in partial recovery of the visual field. Conclusion . Optochiasmal cavernomas are rare, removal can improve visual outcome. 展开更多
关键词 海绵状血管瘤 视交叉 视力丧失 颞侧偏盲 错构瘤 肿瘤疾病 病理检查 神经外科 切除术 损伤诊断
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不典型性眼重症肌无力症
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作者 milea d. Laforet P. +1 位作者 Eymard B. 杨秀梅 《世界核心医学期刊文摘(眼科学分册)》 2005年第10期5-6,共2页
The diagnosis of ocular myasthenia gravis is rarely in doubt in patients with a proper history and typical clinical findings. However, myasthenia gravis can mimick any pupil- sparing eye movement disorder and several ... The diagnosis of ocular myasthenia gravis is rarely in doubt in patients with a proper history and typical clinical findings. However, myasthenia gravis can mimick any pupil- sparing eye movement disorder and several diseases may masquerade myasthenia g ravis. We review the atypical presentations and differential diagnoses in ocular myasthenia gravis, describing four patients with some of these conditions (4th nerve palsy, near spasm reflex, one-and-a-half syndrome, orbital meningioma). The correct interpretation of the clinical findings associated with appropriate neuro-imaging studies allowed the appropriate diagnosis in these cases. 展开更多
关键词 肌无力症 不典型性 重症肌无力 近反射痉挛 眶脑膜瘤 典型病史 脑神经麻痹 鉴别诊断 运动失调 影像学检查
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前交通动脉瘤破裂后出现急性球后视神经病
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作者 Claes C. milea d. +1 位作者 Bodaghi B. 安胜 《世界核心医学期刊文摘(眼科学分册)》 2006年第8期10-11,共2页
Purpose: The vast majority of ruptured aneurysms of the anterior communicating artery typically present with subarachnoid haemorrhage. Isolated visual complaints are very uncommon in this setting. We present an unusua... Purpose: The vast majority of ruptured aneurysms of the anterior communicating artery typically present with subarachnoid haemorrhage. Isolated visual complaints are very uncommon in this setting. We present an unusual case of a patient with an acute retrobulbar optic neuropathy, secondary to a ruptured anterior communicating artery aneurysm. Design: Observational case report. Methods: A 29- year-old woman was assessed for an acute, isolated unilateral optic neuropathy of unknown origin. Although an initial encephalic MRI was believed to be normal, an underlying ruptured anterior communicating artery aneurysm was eventually diagnosed when the patient became stuporous because of intracranial bleeding. Conclusions: Occurrence of an acute retrobulbar optic neuropathy may be the initial isolated sign related to a ruptured anterior communicating artery aneurysm, prompting an appropriate neuroradiological assessment. 展开更多
关键词 交通动脉瘤破裂 球后视神经 蛛网膜下出血 神经学 颅内出血 观察性
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