Sanna M, Zini C
Am J Otol. 1984 Jul;5(5):368-73.
This article is based on a report presented at the Second International Conference on Cholesteatoma and Mastoid Surgery, in Tel Aviv, in March 1981. The principal aim is to illustrate our personal experience with the so-called congenital cholesteatoma of the middle ear, that is, a cholesteatoma growing inside the tympanic cavity affecting subjects with no inflammatory processes in their clinical history and a perfectly normal eardrum. Eleven cases out of a total of 429 cases with cholesteatoma (2.56%) operated on at the Otorhinolaryngology Clinic II of Parma are reported. All patients--nine children and two adults--underwent a combined-approach closed tympanoplasty. The diagnostic stages are analyzed in particular, as well as the clinical and impedance audiometric data, which are correlated with surgical findings. Pathogenetic mechanisms are discussed briefly. The need for screenings to be carried out in schools and an accurate evaluation of all unilateral impairments in hearing conduction are emphasized with a veiw to early diagnosis.
本文基于1981年3月在特拉维夫举行的第二届胆脂瘤和乳突外科学国际会议上发表的一份报告。主要目的是阐述我们在所谓中耳先天性胆脂瘤方面的个人经验,即一种生长在鼓室内的胆脂瘤,其临床病史中无炎症过程且鼓膜完全正常。报告了帕尔马第二耳鼻喉科诊所手术治疗的429例胆脂瘤病例中的11例(2.56%)。所有患者——9名儿童和2名成人——均接受了联合进路闭合式鼓室成形术。特别分析了诊断阶段,以及临床和阻抗测听数据,并将其与手术结果相关联。简要讨论了发病机制。强调了在学校进行筛查以及对所有单侧听力传导障碍进行准确评估以实现早期诊断的必要性。