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伴有传导性耳聋及镫骨切除组织学表现的克-费综合征

Klippel-Feil syndrome with conductive deafness and histological findings of removed stapes.

作者信息

Sakai M, Miyake H, Shinkawa A, Komatsu N

出版信息

Ann Otol Rhinol Laryngol. 1983 Mar-Apr;92(2 Pt 1):202-6. doi: 10.1177/000348948309200222.

Abstract

The Klippel-Feil syndrome is usually associated with sensorineural hearing impairment, but rarely is it associated with conductive or mixed deafness. A 22-year-old female presented with fusion of the cervical vertebrae, torticollis, scoliosis, pterygium colli, the Sprengel deformity with an omovertebral bone, concavity of the thorax and conductive hearing impairment of the right ear. Tympanotomy disclosed an atrophic long process of incus and a fixation of the stapes footplate, and stapedectomy was performed with immediate postoperative improvement of hearing. However, she developed a sudden hearing loss with dizziness soon after she had physical exercise on the 15th postoperative day, and revision surgery revealed a perilymph fistula of the oval window. Histological investigations of the removed stapes showed no specific osseous changes but hyperostosis of the posterior edge of the footplate. The literature is reviewed and the etiology of the conductive deafness and the perilymph fistula is discussed.

摘要

克-费综合征通常与感音神经性听力障碍相关,但很少与传导性或混合性耳聋相关。一名22岁女性,表现为颈椎融合、斜颈、脊柱侧弯、颈蹼、伴有椎动脉的先天性高肩胛畸形、胸廓凹陷以及右耳传导性听力障碍。鼓室切开术发现砧骨长突萎缩和镫骨足板固定,遂行镫骨切除术,术后听力立即改善。然而,术后第15天她在体育锻炼后不久出现突发性听力损失伴头晕,翻修手术发现卵圆窗有外淋巴瘘。切除的镫骨组织学检查未发现特异性骨质改变,但足板后缘骨质增生。本文回顾了相关文献并讨论了传导性耳聋和外淋巴瘘的病因。

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