Król Bartłomiej, Porowski Marek, Cywka Katarzyna B, Skarżyńska Magdalena B, Skarżyński Piotr Henryk
World Hearing Center, Institute of Physiology and Pathology of Hearing, Warsaw/Kajetany, Poland.
Oto-Rhino-Laryngology Surgery Clinic, World Hearing Center, Institute of Physiology and Pathology of Hearing, Warsaw/Kajetany, Poland.
Am J Case Rep. 2020 Nov 10;21:e925914. doi: 10.12659/AJCR.925914.
BACKGROUND Obliteration of the mastoid cavity with S53P4 bioactive glass is becoming a popular method of treatment, allowing most of the problems with the postoperative cavity to be eliminated. In the case of a hearing aid, reconstruction of the posterior wall of the auditory canal is an extremely beneficial procedure and, in the case of the Bonebridge implant, is necessary. After reconstruction, the FMT transducer is covered by bone and bioactive glass and has no contact with the postoperative cavity. The aim of this article is to present a case report. CASE REPORT A 41-year-old male patient with a history of bilateral otitis media with cholesteatoma since childhood had undergone many ear operations since 2001, including radical modified operations and postoperative revisions. There had been ossiculoplasty using own materials and a Kurz TORP prosthesis which gave a short-term hearing improvement for 3 months. The patient underwent tests for implantable devices, which showed a potential significant improvement in hearing and understanding speech. The patient met the audiological criteria qualifying him for the use of an implantable bone conduction device. However, a CT scan of the temporal bone showed that the Bonebridge implant could not be implanted due to insufficient mastoid volume. In order to safely implant the Bonebridge device, it was necessary to first rebuild the posterior wall of the left ear canal. The absolute condition was no inflammation of the ear or leaks for several months. CONCLUSIONS The two-stage surgical procedure as described in this case report can allow the Bonebridge implant to be used in a wider group of patients with previous anatomical limitations.
背景 使用S53P4生物活性玻璃填塞乳突腔正成为一种流行的治疗方法,能消除术后腔隙的大多数问题。对于助听器而言,重建耳道后壁是极其有益的手术,而对于骨桥植入物来说,则是必要的。重建后,FMT换能器被骨和生物活性玻璃覆盖,与术后腔隙无接触。本文旨在呈现一例病例报告。病例报告 一名41岁男性患者,自幼患有双侧胆脂瘤型中耳炎,自2001年以来接受了多次耳部手术,包括改良根治手术和术后修复手术。曾使用自体材料和库尔兹TORP假体进行听骨链成形术,听力在短期内改善了3个月。患者接受了可植入设备测试,结果显示听力和言语理解能力有显著潜在改善。该患者符合使用可植入骨传导设备的听力学标准。然而,颞骨CT扫描显示,由于乳突体积不足,无法植入骨桥植入物。为了安全植入骨桥设备,有必要首先重建左耳耳道后壁。绝对条件是耳朵几个月内无炎症或渗漏。结论 本病例报告中描述的两阶段手术程序可使骨桥植入物应用于更广泛的、先前存在解剖学限制的患者群体。