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Nasal chondromesenchymal hamartoma: an update

Published online by Cambridge University Press:  23 August 2021

T F C Saunders*
Affiliation:
Department of Otolaryngology, Birmingham Children's Hospital, UK
H Bruijnzeel
Affiliation:
Department of Otorhinolaryngology and Head and Neck Surgery, UMC Utrecht, The Netherlands Brain Center Rudolf Magnus, Utrecht, The Netherlands
S Ahmed
Affiliation:
Department of Skull base Surgery, University Hospital Birmingham, UK
M Paruleka
Affiliation:
Department of Ophthalmology, Birmingham Children's Hospital, UK
A-L McDermott
Affiliation:
Department of Otolaryngology, Birmingham Children's Hospital, UK
*
Author for correspondence: Mr T F C Saunders, Department of Otolaryngology (ENT), Birmingham Children's Hospital, Steelhouse Lane, BirminghamB4 6NH, UK E-mail: [email protected]

Abstract

Objective

Nasal chondromesenchymal hamartoma is a rare pathology that can present with a myriad of symptoms to ENT, maxillofacial and ophthalmology departments. This study reviewed the literature on nasal chondromesenchymal hamartoma as well as adding three new cases to the reported literature.

Method

This study was an up-to-date review of the world literature with the addition of three new cases to provide the most comprehensive review to date.

Results

A total of 56 patients with nasal chondromesenchymal hamartoma were identified, ranging from children to adults. Nasal symptoms and ocular symptoms were most common, and surgical resection was the most frequent treatment modality.

Conclusion

This study advocates for increased awareness of the condition associations for nasal chondromesenchymal hamartoma, multi-specialty treatment and the role for the ENT surgeon in treatment of the condition.

Type
Review Article
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of J.L.O. (1984) LIMITED

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Footnotes

Mr T F C Saunders takes responsibility for the integrity of the content of the paper

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