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1
Congenital cholesteatomas are rare disorders, which may originate from the postpartum persistence of epidermoid formations.They have been defined as evidencing no tympanic perforation, that a pearly white mass medial to the tympanic membrane. Usually presentation as asymptomatic but rarely conductive hearing loss, otorrhea, vertigo may occur. Treatment of congenital cholesteatomas is surgical. In this article,we present a case with congenital cholesteatoma presenting hearing loss, otalgia ve otorrhea, also bone defect associated with carotis interna artery.
Congenital cholesteatomas are rare disorders, which may originate from the postpartum persistence of epidermoid formations.They have been defined as evidencing no tympanic perforation, that a pearly white mass medial to the tympanic membrane. Usually presentation as as asymptomatic but rarely conductive hearing loss, otorrhea, vertigo may occur. Treatment of congenital cholesteatomas is surgical. In this article,we present a case with congenital cholesteatoma presenting hearing loss, otalgia and otorrhea, also bone defect associated with carotis interna artery.
Alan : Sağlık Bilimleri
Dergi Türü : Ulusal
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