镫骨肌、肌腱和锥体缺失-再次发现异常

Rachit Sood, A. Bhardwaj, M. Malhotra, M. Priya, Nivedhan Ravichandran, Akhilesh Chandra Yadav, R. Prasath, J. Dave
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引用次数: 0

摘要

先天性镫骨缺失是一种罕见的疾病,发生率为0.5%,在活的患者中报道的病例很少。我们在此报告一例中年女性,双耳漏液,听力下降一年多,检查显示双侧中央穿孔较大,术前听力学检查显示双侧平均听力损失45db,双侧气骨间隙35dB。内镜下完成右侧I型鼓室成形术,发现右侧镫骨肌、肌腱和锥体缺失。镫骨缺失应仔细检查外科医生是否有其他相关异常,如鼓室硬化、固定足板和面神经走行异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absent stapedius muscle, tendon and pyramid – An anomaly revisited
Congenital absence of stapedius is an exquisite entity, with an incidence of 0.5% and very few cases reported in live patients. We herein report a case of a middle-aged female presented with bilateral ear discharge and decreased hearing for more than a year, which, on examination, showed a large central perforation bilaterally, and an audiogram preoperatively revealed an average hearing loss of 45 dB and air-bone gap of 35dB bilaterally. Right endoscopic type I tympanoplasty was done, which unveiled absent stapedius muscle, tendon, and pyramid on the right side. The absent stapedius should circumspect the operating surgeon to look for other associated anomalies such as tympanosclerosis, fixed footplate and aberrant course of the facial nerve.
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