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Multimodality imaging features of hereditary multiple exostoses

Version 2 2024-06-13, 12:59
Version 1 2019-05-17, 09:38
journal contribution
posted on 2024-06-13, 12:59 authored by HK Kok, L Fitzgerald, N Campbell, ID Lyburn, PL Munk, O Buckley, WC Torreggiani
Hereditary multiple exostoses (HME) or diaphyseal aclasis is an inherited disorder characterised by the formation of multiple osteochondromas, which are cartilage-capped osseous outgrowths, and the development of associated osseous deformities. Individuals with HME may be asymptomatic or develop clinical symptoms, which prompt imaging studies. Different modalities ranging from plain radiographs to cross-sectional and nuclear medicine imaging studies can be helpful in the diagnosis and detection of complications in HME, including chondrosarcomatous transformation. We review the role and imaging features of these different modalities in HME.

History

Journal

British journal of radiology

Volume

86

Pagination

1-6

Location

London, Eng.

eISSN

1748-880X

Language

eng

Publication classification

C1 Refereed article in a scholarly journal

Copyright notice

2013, The Authors

Issue

1030

Publisher

British Institute of Radiology

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