伪装成脑脊液鼻漏的内耳畸形-管理的新观点和文献综述。

Nidhin Das K, Vidhu Sharma, Sarbesh Tiwari, Amit Goyal
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引用次数: 0

摘要

自发性脑脊液(CSF)鼻漏是罕见的,可能继发于内耳畸形。在任何出现听力障碍、鼻漏或耳漏的儿科患者中,应考虑CSF泄漏的可能诊断。病例报告:我们描述了一个13个月大的男婴表现为鼻漏,经评估发现是先天性内耳畸形引起的脑脊液耳鼻漏。影像学表现为双侧内耳畸形,左侧脑脊液漏,双侧深度感觉神经性听力丧失。考虑了多学科管理。患儿左侧行脑脊液漏修补术,右侧行人工耳蜗植入。结论:本病例是一个很好的例子,描述了在最近的创新基础上处理脑脊液泄漏内耳异常以解决听觉康复的繁琐。根据现有文献,内耳异常是人工耳蜗候选人群中一个重要的亚群,具有良好的听觉效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Inner Ear Malformation Masquerading as CSF Rhinorrhea - New Perspectives of Management and Literature Review.

Introduction: Spontaneous cerebrospinal fluid (CSF) rhinorrhea is rare and may develop secondary to inner ear malformation. A possible diagnosis of CSF leak should be considered in any Pediatric patient who presents with hearing impairment, rhinorrhea, or otorrhea.

Case report: We describe a case of 13 months male infant presenting with rhinorrhoea which on evaluation found to be CSF oto-rhinorrhoea due congenital inner ear malformation. Imaging showed malformed inner ear on both sides with CSF leak on left side with bilateral profound sensory neural hearing loss. A multidisciplinary management was considered. Child underwent CSF leak repair on left side followed by Cochlear implantation on right side in another setting.

Conclusion: This case is a perfect example to describe the cumbersome management of CSF leak with inner ear anomaly addressing the auditory habilitation on the grounds of recent innovations. As per available literature inner ear anomaly is an important subgroup of population of cochlear implant candidates with promising auditory outcomes.

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来源期刊
Iranian Journal of Otorhinolaryngology
Iranian Journal of Otorhinolaryngology Medicine-Otorhinolaryngology
CiteScore
1.30
自引率
0.00%
发文量
72
审稿时长
12 weeks
期刊最新文献
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