• James Fowler, Ariel Takayanagi, Brian Fiani, Alessandra Cathel, Kasra John Sarhadi, Mohammad Arshad, Sean Lau, Imran Siddiqi, Hammad Ghanchi, Adam Wolberg, and Omid Hariri.
• Department of Neurosurgery, Desert Regional Medical Center, Palm Springs, California, USA.
• World Neurosurg. 2021 May 1; 149: 215-225.e6.

AbstractOsteochondroma is described as a capped benign bony neoplasm that forms on the outer surface of bone. These tumors affect nearly 6 million people per year. Although osteochondromas most often involve the appendicular skeleton, many involve the spine, with many cases located in the cervical spine. When osteochondromas involve the spine, they can present with a variety of symptoms, including pain, radiculopathy, and myelopathy, which may necessitate surgical treatment. Spinal osteochondromas can be classified into 2 types: multiple osteochondromas in the context of patients with multiple hereditary exostosis (MHE) and solitary osteochondroma or solitary exostosis (SE). Previous reviews have captured only some of the available literature on cervical osteochondromas and have generally focused on either SE or those associated with MHE. The purpose of our review was to provide an extensive review of all previously reported cervical osteochondromas and to compare osteochondroma characteristics, clinical presentation, and outcomes in the context of MHE and SE.Copyright © 2021 Elsevier Inc. All rights reserved.

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