Congenital ossicular chain anomaly. Columella stapes

O. Orishchak, D. Orishchak, N. V. Vasilyuk
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Abstract

Congenital anomalies of the ossicular chain are a rare condition in clinical practice. In literature described different variants of the ossicular chain anomaly from stapes footplate ankylosis to complete aplasia of the ossicular chain, oval, and round window. Possible congenital ossicular chain anomaly should be suspected in case of non-progressive conductive hearing loss with a normal ear drum during an otoscopic examination, without a history of previous ear infections or trauma. In this article, we described the clinical case of congenital ossicular chain anomaly presented as fixed incus. Stapes was presented as single, straight, broad crus that were attached to the central part of the footplate. Stapedius tendon was absent. The footplate was completely mobile. Exploratory tympanotomy was performed to confirm a diagnosis of congenital ossicular chain anomaly. The ossicular chain was reconstructed with PORP titanium prosthesis. Furthermore, a literature review was done, conclusions presented.
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先天性听骨链异常。小柱镫骨
摘要先天性听骨链异常在临床上是一种罕见的疾病。文献中描述了听骨链异常的不同变体,从镫骨足板强直到听骨链完全发育不全,椭圆形和圆形窗口。耳镜检查时,若无耳部感染或外伤史的非进行性传导性听力损失,鼓膜正常,应怀疑可能存在先天性听骨链异常。在本文中,我们描述了先天性听骨链异常表现为固定砧骨的临床病例。镫骨表现为单一、直、宽的小腿,附着在底板的中央部分。镫骨肌腱缺失。踏板完全可以移动。探索性鼓室切开术确诊先天性听骨链异常。用PORP钛假体重建听骨链。并对文献进行综述,得出结论。
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