Congenital or Acquired? A Case Report of Extensive Congenital Cholesteatoma

Extensive congenital cholesteatoma
Vol. 5 No. 2 : 2010 (103-107)

Roslenda AR Roslenda AR
Asma A Asma A
Iqbal FRW Iqbal FRW
Jeevanan J Jeevanan J

Abstract
Congenital cholesteatoma (CC) is rare clinical condition and It is known as a pearly white mass medial to an intact tympanic membrane. In this case report, we describe a 6-year-old boy who presented with a one year history of left ear discomfort, reduced hearing, followed by ear discharge two months prior to admission. Otoscopic examination revealed a large attic perforation. Radiological investigation showed extensive cholesteatoma in the mastoid, mesotympanum and epitympanum with destruction of the ossicles including the stapes footplate. He underwent radical mastoidectomy in view of extensive cholesteatoma with tympanoplasty type V. In this case report, the classification, treatment and theories related to CC are discussed.

Keywords : cholesteatoma, deafness, hearing loss, ossicles, tympanoplasty,

Correspondance Address
Dr Roslenda bt Abdul Rahman, Department of ORL Head & Neck Surgery, Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, Bandar Tun Razak, 56000 Cheras, Kuala Lumpur. Tel:+603 9145 6576. Fax: +603 9145 7765. Email: lenda_orl@yahoo.com