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首页> 外文期刊>World neurosurgery >A Case of Ecchordosis Physaliphora in the Prepontine Cistern: A Rare Entity in the Differential Diagnosis of an Epidermoid Cyst
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A Case of Ecchordosis Physaliphora in the Prepontine Cistern: A Rare Entity in the Differential Diagnosis of an Epidermoid Cyst

机译:Prepontine Cistern中肌肉肌肉素的病例:表皮样囊肿差异诊断中的罕见实体

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摘要

Background Ecchordosis physaliphora (EP) is a benign notochordal remnant that is usually asymptomatic. We report a case of a symptomatic large EP mimicking an epidermoid cyst. Case Description A 44-year-old woman presented with right facial dysesthesia. Brain magnetic resonance imaging showed a mass with a diameter of 3.2 cm that was hypointense on T1-weighted imaging, hyperintense on T2-weighted imaging, isointense to hyperintense on diffusion-weighted imaging, and hyperintense on apparent diffusion coefficient map (1.2–1.6?× 10 ?3 mm 2 /second). There was no apparent contrast enhancement. Differential diagnoses included epidermoid cyst, dermoid cyst, EP, chordoma, chondrosarcoma, neurenteric cyst, and arachnoid cyst. Clinicopathologic examination revealed that the mass was an EP. Conclusions EP in the prepontine cistern should be considered in the differential diagnosis of epidermoid cyst. ]]>
机译:背景生蚀肌电蛋白(EP)是一种通常无症状的良性诺奇遗骸。 我们报告了一种模仿表皮囊肿模拟的症状大EP的案例。 案例描述一名44岁女性呈现出正确的面部缺失。 脑磁共振成像显示出直径为3.2cm的质量,在T1加权成像,高速成像上的过敏上,对扩散加权成像的超强,和明显扩散系数图的超敏(1.2-1.6? ×10?3 mm 2 /秒)。 没有明显的对比度增强。 差异诊断包括表皮样囊肿,Dermoid囊肿,EP,脊索瘤,软骨糖瘤,神经插入囊肿和蛛网膜囊肿。 临床病理检查显示群众是EP。 结论在表皮样囊肿的鉴别诊断中应考虑预接受前水箱中的EP。 ]]>

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