Suetake M, Kobayashi T, Takasaka T
Department of Otolaryngology, Tohoku University School of Medicine, Sendai, Japan.
Am J Otol. 1991 Mar;12(2):132-4.
A case of bilateral congenital cholesteatomas, which occurred in a 15-year-old male was reported. His family had been aware of his hearing impairment since he was 3 years old. He had experienced neither otalgia nor otorrhea. Tympanograms were A type bilaterally, and an audiogram showed conductive hearing loss of about 60 dB on both sides. High resolution CT of a horizontal section revealed soft tissue density occupying the space medial to the body of the incus in the right ear, while the middle ear space appeared to be completely clear on the left side. The membranous cholesteatomas on both sides were accompanied by ossicular anomalies with hypoplasia of the long process of incus and the superstructure of the stapes. This case constitutes the seventh case report of bilateral congenital cholesteatomas in the literature. The literature is reviewed and the pathogenesis of congenital cholesteatomas associated with ossicular anomalies is discussed.
报告了一例发生在一名15岁男性的双侧先天性胆脂瘤病例。自他3岁起,其家人就已意识到他有听力障碍。他既没有经历过耳痛也没有耳漏。鼓室图双侧均为A型,听力图显示双侧传导性听力损失约60dB。水平位高分辨率CT显示,右侧砧骨体内侧空间有软组织密度影,而左侧中耳空间似乎完全清晰。双侧膜性胆脂瘤均伴有听骨链异常,砧骨长突和镫骨上部结构发育不全。该病例是文献中双侧先天性胆脂瘤的第七例报告。对文献进行了综述,并讨论了与听骨链异常相关的先天性胆脂瘤的发病机制。