Atrophy of the long process of the incus of unknown origin – a rare cause of acquired conductive hearing loss. Clinical case report and a mini-review of literature

Nikodem Pietrzak, Katarzyna Wiktoria Jankowska, Oskar Rosiak, Wiesław Konopka
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Abstract

Introduction: Among the pediatric population, the most common cause of conductive hearing loss is exudative otitis media. If fluid is not present in the tympanic cavity, an assessment of the middle ear transmission system is recommended. Aim: To present a clinical case of atrophy of the long process of the incus in a 17-year-old patient with a 10-year history of conductive hearing loss, exhibiting an air-bone gap of 30 to 50 dB in the right ear qualified for exploratory tympanotomy. Literature review of internet databases to identify similar clinical cases. Material and methods: CARE guidelines were used to standardize the description of the clinical case. Surgical treatment included an exploratory tympanotomy using an endaural approach, visualizing atrophy of the long process of the incus and the connective tissue band connecting the stapes head to the lateral wall of the tympanic cavity. The eardrum was preserved. An ossiculoplasty was performed using autogenic materials – interposition of the incus. Internet databases PubMed and Scopus were searched using the search string „Incus atrophy” OR „Incus necrosis” AND NOT „Stapedectomy”. Results: On follow-up one month after surgery a hearing improvement was observed with a reduction in air-bone gap to 10–15 dB. No complications were observed. Discussion: Atrophy of the long process of unknown origin is a very rare cause of acquired conductive hearing loss. A review of literature revealed 8 manuscripts describing similar cases, which are presented and discussed in the manuscript. Ossiculoplasty in such cases might be performed using autogenic or artificial materials as partial ossicular prostheses or bone cement. Conclusions: Careful evaluation of imaging studies and hearing tests can often identify a defect in the conductive system; exploratory tympanotomy is often required. In cases such as the one presented, interposition of the incus might be a viable option.
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来源不明的耳根长突的萎缩——获得性传导性听力损失的罕见原因。临床病例报告及文献综述
导读:在儿童人群中,传导性听力损失最常见的原因是渗出性中耳炎。如果鼓室中不存在液体,建议对中耳传输系统进行评估。目的:报告一例17岁的传导性听力损失患者的耳聋长突萎缩,右耳气骨间隙为30 ~ 50db,适合探索性鼓室切开术。查阅互联网数据库的文献,找出相似的临床病例。材料和方法:采用CARE指南规范临床病例描述。手术治疗包括采用硬膜入路的探索性鼓室切开术,观察耳根长突和连接镫骨头与鼓室外侧壁的结缔组织带的萎缩。鼓膜保存完好。使用自体材料植入砧骨进行听骨成形术。检索检索词为“Incus atrophy”或“Incus necrosis”,而非“Stapedectomy”。结果:术后随访1个月,观察到听力改善,气骨间隙减少到10-15 dB。无并发症发生。讨论:来源不明的长突萎缩是获得性传导性听力损失的一个非常罕见的原因。对文献的回顾揭示了8份描述类似病例的手稿,这些手稿在手稿中被提出和讨论。在这种情况下,听骨成形术可以使用自体或人工材料作为部分听骨假体或骨水泥。结论:仔细评估影像学检查和听力测试通常可以识别传导性系统的缺陷;通常需要探索性鼓室切开术。在这种情况下,插入incus可能是一个可行的选择。
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来源期刊
Polish Otorhinolaryngology Review
Polish Otorhinolaryngology Review Medicine-Otorhinolaryngology
CiteScore
0.20
自引率
0.00%
发文量
23
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