Literature DB >> 12196244

Cervical osteochondroma as a cause of spinal cord compression in a patient with hereditary multiple exostoses: Computed tomography and magnetic resonance imaging findings.

Bayram Cirak1, Nevzat Karabulut, Selçuk Palaoglu.   

Abstract

Spinal cord compression is a rare but extremely serious complication of hereditary multiple exostoses (HME). Imaging of the spine is important for surgical planning and follow up. We present CT and MR findings in a male patient with HME who developed spinal cord compression from a cervical osteochondroma. Complete recovery was achieved following surgery.

Entities:  

Mesh:

Year:  2002        PMID: 12196244     DOI: 10.1046/j.1440-1673.2002.01067.x

Source DB:  PubMed          Journal:  Australas Radiol        ISSN: 0004-8461


  6 in total

1.  Subclinical cervical osteochondroma presenting as brown-sequard syndrome after trivial neck trauma.

Authors:  Jin-Young Lee; Soo-Bin Im; Kwan-Woong Park; Dong-Seong Shin
Journal:  J Korean Neurosurg Soc       Date:  2012-04-30

2.  Solitary thoracic osteochondroma presenting as Brown-Séquard syndrome.

Authors:  Raghvendra Vijayrao Ramdasi; Amit Mahore
Journal:  BMJ Case Rep       Date:  2014-11-17

3.  Spinal stenosis frequent in children with multiple hereditary exostoses.

Authors:  Ali Ashraf; A Noelle Larson; Gabriela Ferski; Cary H Mielke; Nicholas M Wetjen; Kenneth J Guidera
Journal:  J Child Orthop       Date:  2013-02-19       Impact factor: 1.548

4.  Cervical osteochondroma presenting as brown-sequard syndrome in a child with hereditary multiple exostosis.

Authors:  In-Ho Han; Sung-Uk Kuh
Journal:  J Korean Neurosurg Soc       Date:  2009-05-31

5.  Giant cervical spine osteochondroma in an adolescent female.

Authors:  N Huda; M Julfiqar; Ajay Pant; Tariq Jameel
Journal:  J Clin Diagn Res       Date:  2014-05-15

6.  Solitary lower lumbar osteochondroma (spinous process of L3 involvement): a case report.

Authors:  Ebrahim Ghayem Hassankhani
Journal:  Cases J       Date:  2009-12-20
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.