Hu Chih-Yu, Chen Shih-Lung, Zhang Bang-Yan, Chan Kai-Chieh
Division of Otology, Department of Otolaryngology-Head and Neck Surgery, Chang Gung Memorial Hospital, Linkou, Taiwan.
School of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Ear Nose Throat J. 2024 Jul 26:1455613241266689. doi: 10.1177/01455613241266689.
Osteomas in the external auditory canal (EAC) can lead to stenosis, and impair epithelium migration and self-cleaning capability, thereby trapping keratinized epithelium and triggering the development of cholesteatoma. Our study aims to identify the risk of cholesteatoma development in patients with osteoma and proposes a stepwise approach to managing patients with EAC osteoma. The maximum diameter of the osteoma was measured in axial and coronal views on high-resolution computed tomography (HRCT). We calculated the relative obstruction ratio caused by the osteoma in the axial and coronal views. Prior to surgery, otoscopy was employed to identify pedicle formation. The patients were categorized into 2 groups based on the presence of cholesteatoma. We identified 43 patients diagnosed with EAC osteoma. A total of 9 (20.9%) patients with EAC osteomas developed cholesteatoma and the other 34 (79.1%) did not. The maximum diameter of osteomas with and without cholesteatoma was 12.67 ± 4.09 and 7.67 ± 3.27 mm, respectively ( < .001). In the group without cholesteatoma, 21 osteomas had pedicles while the other 13 did not. In the cholesteatoma group, 2 osteomas had pedicles and 7 did not ( = .037). No difference was observed in the relative obstruction ratio between these 2 groups. Our findings indicate that larger osteomas are more likely to develop cholesteatoma, while the formation of a pedicle may reduce the occurrence of cholesteatoma. In symptomatic patients, preoperative evaluation, including HRCT and otoscopy, is vital for assessing the extent of the osteoma and the potential coexistence of cholesteatoma. These factors are critical for preoperative consultations and surgical planning.
外耳道(EAC)骨瘤可导致狭窄,并损害上皮细胞迁移和自我清洁能力,从而使角化上皮滞留并引发胆脂瘤的形成。我们的研究旨在确定骨瘤患者发生胆脂瘤的风险,并提出一种逐步管理EAC骨瘤患者的方法。在高分辨率计算机断层扫描(HRCT)的轴位和冠状位视图上测量骨瘤的最大直径。我们计算了骨瘤在轴位和冠状位视图上引起的相对阻塞率。手术前,采用耳镜检查确定蒂的形成。根据是否存在胆脂瘤将患者分为两组。我们确定了43例被诊断为EAC骨瘤的患者。共有9例(20.9%)EAC骨瘤患者发生了胆脂瘤,另外34例(79.1%)未发生。有胆脂瘤和无胆脂瘤的骨瘤最大直径分别为12.67±4.09和7.67±3.27mm(<.001)。在无胆脂瘤组中,21个骨瘤有蒂,另外13个没有。在胆脂瘤组中,2个骨瘤有蒂,7个没有(=.037)。两组之间的相对阻塞率没有差异。我们的研究结果表明,较大的骨瘤更容易发生胆脂瘤,而蒂的形成可能会降低胆脂瘤的发生率。对于有症状的患者,包括HRCT和耳镜检查在内的术前评估对于评估骨瘤的范围以及胆脂瘤的潜在共存情况至关重要。这些因素对于术前会诊和手术规划至关重要。