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Congenital cholesteatoma of the mastoid temporal bone.

机译:乳突颞骨先天性胆脂瘤。

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OBJECTIVE: Congenital mastoid cholesteatomas are rare lesions of the temporal bone. The clinical presentation of these lesions is variable, making them difficult to identify preoperatively. We evaluated our series of mastoid congenital cholesteatomas (CCs) in an effort to better define the clinical presentation, imaging characteristics, and surgical challenges specific to this lesion. STUDY DESIGN: Retrospective chart and radiologic study review. METHODS: The medical records of patients with the diagnosis of mastoid CC on radiologic imaging over a 15-year period were reviewed. All had surgical and pathologic confirmation. Eight patients underwent preoperative computed tomography (CT). Six also underwent magnetic resonance (MR) scanning. Demographic information, clinical presentation, imaging results, and operative findings were recorded. RESULTS: Nine patients with the diagnosis of mastoid CC satisfying the inclusion criteria were found. Clinical findings were variable, with the most common presentation being an incidental finding. Imaging findings were more uniform. All CT scans demonstrated an expansile, well-circumscribed mass centered within the mastoid portion of the temporal bone. All MR scans showed a well-circumscribed mass with high intensity on T2-weighted images with precontrasted T1 sequences showing the lesion to be isointense or slightly hyperintense to cerebrospinal fluid (CSF). Operative findings included lateral mastoid cortex erosion, sigmoid sinus exposure, ossicular destruction, facial nerve exposure, and associated postauricular abscess. Management of these lesions is reviewed. CONCLUSION: Congenital mastoid cholesteatomas have a variable and nonspecific clinical presentation. Surgical challenges arise from the indolent nature of this clinical entity, which belies the extent of otologic involvement. Imaging with CT and magnetic resonance imaging are diagnostic, defines the extent of these lesions, and facilitates preoperative surgical planning.
机译:目的:先天性乳突胆脂瘤是颞骨的罕见病变。这些病变的临床表现是可变的,使得它们在术前难以识别。我们评估了我们的一系列乳突先天性胆脂瘤(CC),以更好地定义针对该病变的临床表现,影像学特征和手术挑战。研究设计:回顾性图表和放射学研究回顾。方法:回顾性分析15年来经影像学检查诊断为乳突CC的患者的病历。所有患者均经手术和病理证实。八名患者接受了术前计算机断层扫描(CT)。六人也进行了磁共振(MR)扫描。记录人口统计信息,临床表现,影像学结果和手术结果。结果:发现9例乳突CC符合入组标准的患者。临床发现是可变的,最常见的表现是偶然发现。影像学检查结果更为一致。所有CT扫描均显示位于颞骨乳突部分中心的可扩展的,界限清楚的肿块。所有MR扫描均在T2加权图像上显示出边界清楚的肿块,且具有高强度,且预先对比的T1序列显示病变对脑脊液(CSF)等渗或略高渗。手术发现包括乳突外侧皮质侵蚀,乙状窦暴露,听骨破坏,面神经暴露以及相关的耳后脓肿。这些病变的管理进行了审查。结论:先天性乳突胆脂瘤具有可变且非特异性的临床表现。外科挑战来自该临床实体的惰性,这掩盖了耳科的程度。 CT成像和磁共振成像具有诊断意义,可确定这些病变的范围,并有助于术前手术计划。

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