Jahnke V, Falk W
Laryngol Rhinol Otol (Stuttg). 1976 Jul;55(7):556-60.
Middle ear cholesteatoma in childhood is discussed on the basis of 117 operated cases. Early diagnosis was rare, even after fetid otorrhea of long duration; occassionally they presented as acute mastoiditis. The cholesteatoma occurred mostly in older children (90%) and extended to the antrum (73%) or beyond it (54%), with destruction of the ossicles (77%); the hearing often remained normal. Tympanic membrane perforations were usually small, relatively often they were central. More than 50% of the children had normal mastoid pneumatization, usually there were no typical radiological signs of cholesteatoma. Tympanoplasty was most frequently type III (68.5%), the postoperative hearing gain in this group was 47.3%. Residual or recurrent cholesteatoma occurred in 8.5%.
基于117例手术病例对儿童中耳胆脂瘤进行了讨论。早期诊断罕见,即使在长期恶臭耳漏之后;偶尔表现为急性乳突炎。胆脂瘤大多发生于较大儿童(90%),并扩展至鼓窦(73%)或其以外(54%),伴有听小骨破坏(77%);听力常保持正常。鼓膜穿孔通常较小,相对常见于中央部。超过50%的儿童乳突气化正常,通常无胆脂瘤的典型影像学征象。鼓室成形术最常见的是Ⅲ型(68.5%),该组术后听力提高率为47.3%。残余或复发性胆脂瘤发生率为8.5%。