Sudhoff H, Liang J, Dazert S, Borkowski G, Michaels L
Hals-Nasen-Ohrenklinik, Ruhr-Universität Bochum, St. Elisabeth Hospital.
Laryngorhinootologie. 1999 Feb;78(2):63-7. doi: 10.1055/s-2007-996832.
Many theories have been suggested regarding the origin, pathogenesis, diagnosis, and incidence of congenital cholesteatoma.
An overview on the current literature on congenital cholesteatoma of the middle ear is presented. It comprises the possible etiology and pathogenesis of congenital cholesteatoma. Among other theories, germ scattering, metaplasia, ingrowth of meatal epidermis, and reflux of amniotic fluid have been proposed. Special emphasis is put on the epidermoid formation theory, which has been described by Michaels and others.
It is widely accepted that congenital cholesteatomas may originate from the postpartum persistence of epidermoid formations. Nevertheless, a clear transition from epidermoid formation to congenital cholesteatoma has yet to be confirmed.
关于先天性胆脂瘤的起源、发病机制、诊断及发病率,已提出诸多理论。
本文对当前中耳先天性胆脂瘤的文献进行了概述。内容包括先天性胆脂瘤可能的病因及发病机制。除其他理论外,还提出了胚芽播散、化生、外耳道表皮内陷及羊水反流等理论。特别强调了由迈克尔斯等人描述的表皮样形成理论。
先天性胆脂瘤可能源于产后表皮样结构的持续存在,这一观点已被广泛接受。然而,表皮样形成向先天性胆脂瘤的明确转变尚待证实。