Literature DB >> 10739291

Clinical and radiographic analysis of osteochondromas and growth disturbance in hereditary multiple exostoses.

D E Porter1, M E Emerton, F Villanueva-Lopez, A H Simpson.   

Abstract

Hereditary multiple exostoses (HME) is traditionally described as a skeletal dysplasia. However, the discovery that the EXT family of tumour suppressor genes are responsible for HME suggests that it is more appropriate to classify HME as a familial neoplastic trait. In a clinical and radiographic analysis of paired bone length and exostoses number and dimensions in a HME cohort, the local presence of osteochondromas was consistently associated with growth disturbance. In particular, an inverse correlation between osteochondroma size and relative bone length (p<0.01) was found. These data suggest that the growth retardation in HME may result from the local effects of enlarging osteochondromas rather than a skeletal dysplasia effect. This study provides the first clinical rationale for ablation of rapidly enlarging exostoses to reduce growth disturbance.

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Mesh:

Year:  2000        PMID: 10739291

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  15 in total

Review 1.  The link between heparan sulfate and hereditary bone disease: finding a function for the EXT family of putative tumor suppressor proteins.

Authors:  G Duncan; C McCormick; F Tufaro
Journal:  J Clin Invest       Date:  2001-08       Impact factor: 14.808

2.  Management of forearm deformities with ulnar shortening more than 15 mm caused by hereditary multiple osteochondromas.

Authors:  Zhong-wen Tang; Yi-lun Cao; Tang Liu; Tao Chen; Xiang-sheng Zhang
Journal:  Eur J Orthop Surg Traumatol       Date:  2012-07-01

3.  Malignant degeneration of a lumbar osteochondroma into a chondrosarcoma which mimicked a large retropertioneal mass.

Authors:  Evgeny Strovski; Rola Ali; Douglas A Graeb; Peter L Munk; Silvia D Chang
Journal:  Skeletal Radiol       Date:  2012-04-22       Impact factor: 2.199

4.  Solitary osteochondroma of the twelfth rib with intraspinal extension and cord compression in a middle-aged patient.

Authors:  Jung Hyun Shim; Choon Keun Park; Seung Ho Shin; Hee Sun Jeong; Jang Hoe Hwang
Journal:  BMC Musculoskelet Disord       Date:  2012-04-13       Impact factor: 2.362

5.  Hereditary multiple exostoses in the hands and fingers: early presentation and early surgical treatment in family members. Case reports.

Authors:  Rika Ohkuma; Edward F McCarthy; E Gene Deune
Journal:  Hand (N Y)       Date:  2010-11-23

Review 6.  An update on the imaging of diaphyseal aclasis.

Authors:  Mostafa Ellatif; Ban Sharif; Daniel Lindsay; Robin Pollock; Asif Saifuddin
Journal:  Skeletal Radiol       Date:  2021-04-01       Impact factor: 2.199

7.  Forearm Hereditary Multiple Exostosis: A Retrospective Case Series Study.

Authors:  Nizar Hamdi; Hatan Mortada; Zainab Al Eid; Anas M Makhdoum
Journal:  Cureus       Date:  2022-06-17

Review 8.  Osteochondromas: An Updated Review of Epidemiology, Pathogenesis, Clinical Presentation, Radiological Features and Treatment Options.

Authors:  Kostas Tepelenis; Georgios Papathanakos; Aikaterini Kitsouli; Theodoros Troupis; Alexandra Barbouti; Konstantinos Vlachos; Panagiotis Kanavaros; Panagiotis Kitsoulis
Journal:  In Vivo       Date:  2021 Mar-Apr       Impact factor: 2.155

9.  Multiple hereditary osteochondromatosis: a case report.

Authors:  Cigdem Küçükesmen; Bugra Ozen; Mustafa Akçam
Journal:  Eur J Dent       Date:  2007-07

10.  A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis.

Authors:  C Y Xiao; J Wang; S Z Zhang; W Van Hul; W Wuyts; W M Qiu; H Wu; G Zhang
Journal:  Br J Cancer       Date:  2001-07-20       Impact factor: 7.640

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