An unusual example of hereditary multiple exostoses: a case report and review of the literature.

BMC Musculoskelet Disord

Human Anatomy Resource Centre, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, L69 3GE, UK.

Published: January 2021

Background: Hereditary multiple exostoses (HME) is a rare skeletal disorder characterised by a widespread. distribution of osteochondromas originating from the metaphyses of long bones.

Case Presentation: This case study examines a 55-year-old male cadaver bequeathed to the University of Liverpool who suffered from HME, thus providing an exceptionally rare opportunity to examine the anatomical changes associated with this condition.

Conclusions: Findings from imaging and dissection indicated that this was a severe case of HME in terms of the quantity and distribution of the osteochondromas and the number of synostoses present. In addition, the existence of enchondromas and the appearance of gaps within the trabeculae of affected bones make this a remarkable case. This study provides a comprehensive overview of the morbidity of the disease as well as adding to the growing evidence that diseases concerning benign cartilaginous tumours may be part of a spectrum rather than distinct entities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818741PMC
http://dx.doi.org/10.1186/s12891-021-03967-6DOI Listing

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