An uncommon “third window” in retrofenestral otosclerosis

G. Zambonini, S. Ghiselli, G. Di Trapani, R. Maroldi, D. Cuda
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Abstract

Otosclerosis is an otologic disease characterized by disordered resorption and deposition of the otic capsule bone. It can lead to progressive conductive, mixed or sensorineural Hearing Loss (HL). In rare cases, it manifests itself with a tendency for massive bone resorption with subsequent formation of cavities (“cavitating otosclerosis”). Cavities can sometimes realize communication between the Cerebrospinal Fluid (CSF) at the Internal Auditory Canal (IAC) and the cochlear duct. In these uncommon cases, a “third-window” phenomenon may be established as a concomitant cause of conductive HL. Therefore, the feasibility of stapes surgery should be evaluated, without underestimating the risk of gusher complications. In this report, we discuss the case of a female patient affected by cavitating otosclerosis realizing a connection between IAC and cochlear duct, with mixed hearing loss.
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窗后耳硬化的罕见“第三窗”
耳硬化是一种以耳囊骨吸收和沉积紊乱为特征的耳科疾病。可导致进行性传导性、混合性或感音神经性听力损失(HL)。在极少数情况下,它表现为大量骨吸收的趋势,随后形成空洞(“空化性耳硬化”)。腔体有时可以实现内耳道(IAC)的脑脊液(CSF)与耳蜗管之间的通信。在这些不常见的病例中,“第三窗口”现象可能是导电性HL的伴随原因。因此,应评估镫骨手术的可行性,同时不要低估喷涌并发症的风险。在本报告中,我们讨论了一例女性患者空化性耳硬化,实现了IAC与耳蜗管之间的连接,并伴有混合性听力损失。
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