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与复发性脑膜炎相关的先天性内耳畸形。

Congenital malformation of the inner ear associated with recurrent meningitis.

作者信息

Kimitsuki T, Inamitsu M, Komune S, Komiyama S

机构信息

Department of Otorhinolaryngology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Eur Arch Otorhinolaryngol. 1999;256 Suppl 1:S11-4. doi: 10.1007/pl00014144.

Abstract

Congenital deformities of the labyrinth of the inner ear can be associated with meningitis and varying degrees of hearing loss or deafness. A recurrence of meningitis is due to the development of a fistulous communication between the subarachnoid space and the middle ear cavity, and can prove lethal. An illustrative case of a 4-year-old Japanese girl with bilateral severe hearing loss, recurrent meningitis and malformations of the inner ear and stapes footplate is presented. Removal of the stapes during tympanotomy provoked a gush of cerebrospinal fluid. The defect was repaired successfully, and there has been no further episodes of meningitis to date.

摘要

内耳迷路的先天性畸形可能与脑膜炎以及不同程度的听力损失或耳聋有关。脑膜炎复发是由于蛛网膜下腔与中耳腔之间形成了瘘管相通,可能会致命。本文介绍了一名4岁日本女孩的典型病例,她患有双侧严重听力损失、复发性脑膜炎以及内耳和镫骨足板畸形。鼓室切开术中切除镫骨时引发了脑脊液涌出。缺损成功修复,迄今为止未再发生脑膜炎。

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