Literature DB >> 17006343

Congenital cholesteatoma in a case of congenital aural atresia.

Robert J Caughey1, Robert A Jahrsdoerfer, Bradley W Kesser.   

Abstract

OBJECTIVE: A congenital cholesteatoma arising in the setting of congenital aural atresia is described. This represents the first case reported in the literature. STUDY
DESIGN: Case report.
SETTING: Tertiary otologic referral center, University of Virginia Health System, Charlottesville, Virginia. PATIENT: Eight-year-old patient with unilateral congenital aural atresia.
INTERVENTIONS: Preoperative computer tomographic scanning and surgical atresia repair with removal of cholesteatoma. MAIN OUTCOME MEASURES: Recurrence of cholesteatoma; epithelialized ear canal; hearing improvement.
RESULTS: A congenital cholesteatoma located medial to the ossicular mass in a child with congenital aural atresia was removed, with no evidence of recurrent disease at a revision operation 1 year later. Hearing was improved to a speech reception threshold of 25 dB.
CONCLUSION: Congenital cholesteatoma can arise medial to the ossicular mass in congenital aural atresia. This finding lends support to the epidermoid rest theory for the cause of congenital cholesteatoma.

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Year:  2006        PMID: 17006343     DOI: 10.1097/01.mao.0000232005.08740.d1

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  1 in total

1.  Congenital cholesteatoma of the infratemporal fossa with congenital aural atresia and mastoiditis: a case report.

Authors:  Mosaad Abdel-Aziz
Journal:  BMC Ear Nose Throat Disord       Date:  2012-06-25
  1 in total

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