Congenital Cholesteatoma.

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Congenital Intralabyrinthine Cholesteatoma

A patient with a congenital intralabyrinthine cholesteatoma is presented. High-resolution computerized tomographic scans and intraoperative photomicrographs display features of intralabyrinthine extension. We discuss pathogenetic theories for the development of congenital intralabyrinthine cholesteatoma. The distinction of this condition from congenital cholesteatoma with labyrinthine erosion i...

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Cochlear implant and congenital cholesteatoma

BACKGROUND The occurence of cholesteatoma and cochlear implant is rare. Secondary cholesteatomas may develop as a result of cochlear implant surgery. Primarily acquired cholesteatoma is not typically associated with congenital sensorineural hearing loss or cochlear implant in children. The occurrence of congenital cholesteatoma during cochlear implant surgery has never been reported before, par...

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Congenital cholesteatoma: classification, management, and outcome.

OBJECTIVES To assess whether a classification system for congenital cholesteatoma (CC) can be derived from analysis of a large clinical sample of cases and to assess whether such a classification system is a reliable guide for surgical intervention, reexploration, and hearing outcome. DESIGN A retrospective review of clinical and surgical records of 119 patients with CC. SETTING Four tertia...

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The classic presentation of congenital cholesteatoma is a pearl behind the anterior-superior quadrant of an intact tympanic membrane. Idiopathic hemotympanum is characterized by a dark blue eardrum, the most prominent feature of which is the presence of cholesterol granulomas. Blue eardrum is associated with eustachian tube dysfunction. Despite the well-established relationship between eustachi...

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ژورنال

عنوان ژورنال: Practica Oto-Rhino-Laryngologica

سال: 1995

ISSN: 1884-4545,0032-6313

DOI: 10.5631/jibirin.88.1238