Banakis Hartl Renee M, Said Sherif, Mann Scott E
1 Department of Otolaryngology, University of Colorado School of Medicine, Aurora, CO, USA.
2 Department of Pathology, University of Colorado School of Medicine, Aurora, CO, USA.
Ann Otol Rhinol Laryngol. 2019 Apr;128(4):360-364. doi: 10.1177/0003489418821700. Epub 2019 Jan 4.
: To describe a case of bilateral ear canal cholesteatomas in the setting of underlying first branchial cleft cyst anomalies and to review the pathophysiology underlying the development of external auditory canal cholesteatomas from branchial cleft cyst abnormalities.
: We present a case study of a 61-year-old man who presented with chronic right-sided hearing loss and left-sided postauricular drainage. Clinical evaluation, radiographic work-up, and pathologic analysis confirmed a diagnosis of bilateral ear canal cholesteatoma in the setting of underlying first branchial cleft cyst anomalies. The patient's clinical course, surgical treatment, and management considerations are discussed here.
: Ear canal cholesteatoma represents a rare clinical disease entity deserving a thorough initial assessment. Careful consideration of underlying diseases that result in chronic inflammation, such as branchial cleft lesions, should be included in the differential diagnosis of idiopathic canal cholesteatoma in the absence of prior otologic surgery or trauma.
描述一例在存在第一鳃裂囊肿异常的情况下双侧外耳道胆脂瘤病例,并回顾由鳃裂囊肿异常发展为外耳道胆脂瘤的病理生理学。
我们报告一例61岁男性病例,该患者表现为慢性右侧听力损失和左侧耳后引流。临床评估、影像学检查及病理分析证实诊断为在存在第一鳃裂囊肿异常情况下的双侧外耳道胆脂瘤。在此讨论该患者的临床病程、手术治疗及管理考量。
外耳道胆脂瘤是一种罕见的临床疾病实体,值得进行全面的初始评估。在没有既往耳部手术或外伤的情况下,特发性外耳道胆脂瘤的鉴别诊断应仔细考虑导致慢性炎症的潜在疾病,如鳃裂病变。