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Congenital cholesteatoma of occipital bone or intradiploic epidermoid cyst? One and the same disease

Published online by Cambridge University Press:  25 June 2008

M P A Clark*
Affiliation:
Department of ENT, John Radcliffe Hospital, Oxford
P M Pretorius
Affiliation:
Department of Neuroradiology, John Radcliffe Hospital, Oxford
D Beaumont
Affiliation:
ENT Department, The Medical Specialist Group, St Martin's, Guernsey
C A Milford
Affiliation:
Department of ENT, John Radcliffe Hospital, Oxford
*
Address for correspondence: Mr Matthew P A Clark, 239 Woodstock Rd, Oxford OX2 7AD, UK. E-mail: [email protected]

Abstract

Objective:

We report an extremely rare case of congenital cholesteatoma affecting the occipital bone.

Methods:

We present a case report, plus a review of the world literature on similar lesions.

Results:

This case report describes the presentation and treatment of a congenital cholesteatoma arising in an apparently unique location within the occipital bone, with no effect on middle-ear structure or function. The different imaging characteristics of this lesion are described and illustrated. The discussion centres on the differentiation of this lesion from intradiploic epidermoid cysts, more commonly described in the neurosurgical literature. The possible methods of pathogenesis are discussed, along with treatment suggestions.

Conclusion:

Congenital cholesteatomas and intradiploic epidermoid cysts are indistinguishable both histologically and radiologically, and would appear to be the same disease.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2008

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References

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