Department of Otolaryngology, Universidade Federal de São Paulo/Escola Paulista de Medicina (UNIFESP/EPM) - São Paulo, SP, Brazil.
Department of Otolaryngology, Head and Neck Surgery, University of Minnesota - Minneapolis, Minnesota, USA.
Otol Neurotol. 2019 Sep;40(8):e839-e846. doi: 10.1097/MAO.0000000000002356.
The presence of bony inner ear malformations may associate with a number of anatomical abnormalities affecting the middle ear structures. Those malformations may create pitfalls and complications for cochlear implantation.
Inner ear malformations associate with varying degrees of hearing loss, and frequently require cochlear implantation for hearing rehabilitation. Therefore, the abnormalities affecting the middle- and inner-ear structures may increase the risk of surgical complications.
We examined 38 human temporal bones from donors with bony inner ear malformations. Using light microscopy, we analyzed the presence of abnormalities in the structures of the middle- and inner-ear.
Our collection comprises of 38 specimens with inner-ear malformations (cochlear aplasia, n = 3; cochlear hypoplasia, n = 30; incomplete partition, n = 3; isolated vestibular malformation, n = 2). The anatomy of the middle ear was abnormal in most temporal bones with cochlear aplasia, cochlear hypoplasia, and incomplete partition type I (40%-100%). Some of those abnormalities (hypoplastic or obliterated mastoid, 55.2%; aplastic or obliterated round window, 71.0%; aberrant course of the facial nerve, 36.8%) may hinder the access to the round window using the conventional facial recess approach for cochlear implantation. The cochlear nerve and associated bony structures (internal auditory canal and bony canal for cochlear nerve) were normal in 71.0% of all temporal bones with inner ear malformations.
Each different type of malformation may create specific surgical challenges to surgeons. Comprehensive preoperative imaging is fundamental toward the surgical success of cochlear implants in patients with malformations. Alternatives to circumvent those middle- and inner-ear abnormalities and potential complications are further discussed.
内耳骨畸形的存在可能与影响中耳结构的许多解剖异常有关。这些畸形可能为耳蜗植入带来陷阱和并发症。
内耳畸形与不同程度的听力损失有关,通常需要进行耳蜗植入以进行听力康复。因此,影响中耳和内耳结构的异常可能会增加手术并发症的风险。
我们检查了 38 例来自有内耳骨畸形供体的人颞骨。使用光学显微镜,我们分析了中耳和内耳结构异常的存在。
我们的标本集合包括 38 例内耳畸形(耳蜗发育不全,n=3;耳蜗发育不全,n=30;不完全分隔,n=3;孤立性前庭畸形,n=2)。大多数具有耳蜗发育不全、耳蜗发育不全和不完全分隔 I 型的颞骨中,中耳解剖异常(占 40%-100%)。这些异常中的一些(发育不良或闭塞的乳突,55.2%;发育不良或闭塞的圆窗,71.0%;面神经异常走行,36.8%)可能会阻碍常规经面神经隐窝入路进行圆窗植入。所有内耳畸形的颞骨中,71.0%的耳蜗神经和相关骨结构(内听道和耳蜗神经骨管)正常。
每种不同类型的畸形都可能给外科医生带来特定的手术挑战。全面的术前成像对于畸形患者耳蜗植入的手术成功至关重要。进一步讨论了规避这些中耳和内耳异常及潜在并发症的替代方案。