Congenital cholesteatoma of the petrous pyramid

ORL J Otorhinolaryngol Relat Spec. 1993 Jul-Aug;55(4):236-9. doi: 10.1159/000276430.

Abstract

A congenital cholesteatoma arising from the petrous pyramid is rarely encountered, and we report a case of such a cholesteatoma in a 23-year-old male. This cholesteatoma was successfully removed by a middle cranial fossa approach. The cholesteatoma showed a unique mode of spread, that is, it originated from the pyramidal apex and extended in two directions: through the facial canal to the tympanic sinus, and along the tympanic tegmen to the mastoid antrum. We discuss the importance of CT and MRI for achieving a diagnosis, as well as the merits of using a middle cranial fossa approach for the surgical excision of this cholesteatoma.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Cholesteatoma / congenital*
  • Cholesteatoma / diagnosis
  • Cholesteatoma / surgery
  • Facial Paralysis / etiology
  • Hearing Loss / etiology
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Petrous Bone*
  • Tomography, X-Ray Computed