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Temporal bone chondroblastoma: big and small

Published online by Cambridge University Press:  29 June 2007

H. K. Leong ,
P. Y. Chong  and
R. Sinniah
H. K. Leong*
Affiliation:
Department of Otorhinolaryngology, National University Hospital, Singapore.
P. Y. Chong
Affiliation:
Department of Pathology, National University Hospital, Singapore.
R. Sinniah
Affiliation:
Department of Pathology, National University Hospital, Singapore.
*
Mr H. K. Leong, Senior Lecturer and Consultant, Department of Otorhinolaryngology, National University Hospital, 5 Lower Kent Ridge Road, Singapore0511. Fax: 65–775–3820.
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Abstract

Chondroblastoma represents approximately one per cent of all primary bone tumours. It is even rarer in the temporal bone and so far only 34 cases have been reported. We report here two cases with chondroblastoma of the temporal bone. The first case was discovered as a small lesion of the attic and root of zygoma. It was removed via mastoidectomy and reconstruction of the bony defect achieved normal external ear canal anatomy and hearing post-operatively. The second case presented as an advanced tumour involving the infratemporal fossa and parapharyngeal space. It was treated surgically via the infratemporal fossa approach. As clear surgical margins were not obtained, post-operative radiotherapy was also given to minimize the chance of recurrence.

Keywords

Temporal boneChondroblastoma
Type
Pathology in Focus
Information
The Journal of Laryngology & Otology , Volume 108 , Issue 12 , December 1994 , pp. 1115 - 1119
Copyright
Copyright © JLO (1984) Limited 1994

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