Atypical presentation of congenital cholesteatoma in an adult case with good hearing result☆

نویسندگان

  • Fevzi Solmaz
  • Davut Akduman
  • Mehmet Haksever
  • Ercan Gündoğdu
  • Atilla Mescioğlu
چکیده

INTRODUCTION Congenital cholesteatoma is thought to be caused by inadequate folding of the epidermoid formation inside the middle ear cleft. During development of the middle ear mucosa, stratified squamous epithelium accumulates in the embryonic life. Its typical appearance is a "pearl" beneath the anterosuperior quadrant of the tympanic membrane. PRESENTATION OF CASE We report 28 years-old case with congenital cholesteatoma in the posterosuperior quadrant of middle ear cavity. The main complaint was the hearing loss which had developed slowly over several years. DISCUSSION The case was surgically treated. Postoperative hearing result was satisfactory. CONCLUSION Congenital cholesteatoma may occur in atypical locations and ages. Many authors prefer canal wall down tympanomastoidectomy. But it can also be treated successfully by intact canal wall tympanomastoidectomy with good hearing results.

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عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2015