A 9-year-old boy with multiple osteochondromas developed progressive transverse myelopathy. Magnetic resonance imaging and CT demonstrated an exostosis at C7-T1 with cord compression.
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http://dx.doi.org/10.1097/00004728-199001000-00025 | DOI Listing |
Cureus
October 2024
Department of Orthopaedics, St. John's Medical College and Hospital, Bangalore, IND.
A 22-year-old man presented to us with back pain for four months, inability to walk, and weakness in both lower limbs. Clinical examination revealed multiple swellings in the body, motor weakness, paresthesia, and upper motor neuron signs. Both magnetic resonance imaging (MRI) and computed tomography (CT) revealed an abnormal bone mass protruding into the spinal canal from the posterior aspect of the ninth rib through the D9-D10 neural foramen.
View Article and Find Full Text PDFSpinal Cord Ser Cases
August 2024
Department of Neurosurgery, Trauma and Burns Center, Ben Arous, Tunisia.
Introduction: Osteochondromas, also known as osteocartilaginous exostosis, are among the most common benign cartilaginous bone tumors, primarily occurring as solitary lesions. While typically found in long bones, spinal involvement is rare, accounting for only a small percentage of benign lesions in this location. Solitary osteochondromas responsible for spinal cord compression are seldom.
View Article and Find Full Text PDFSurg Neurol Int
November 2023
Department of Neurosurgery, Federal University of Ceará, Sobral, Ceará, Brazil.
Background: Hereditary multiple osteochondromas (HMOs) are a rare genetic disorder characterized by the formation of multiple benign osteochondromas that can undergo malignant transformation into chondrosarcoma.
Case Description: A 24-year-old male with a history of HMO and osteochondroma surgery 4 years ago, presented with back pain and paresthesias. The magnetic resonance showed a right paravertebral infiltrating mass at the T12-L1 level causing spinal cord compression.
J Comp Pathol
August 2023
Department of Anatomy, Embryology and Animal Genetics, Veterinary Faculty, University of Zaragoza, 177 Miguel Servet Street, 50013 Zaragoza, Spain. Electronic address:
Feline osteochondromatosis is a spontaneous osteocartilaginous exostosis associated with feline leukaemia virus (FeLV) infection or due to a frameshift variant in the exostosin glycosyltransferase 1 (EXT1) gene. Osteochondromatosis was diagnosed in an indoor-only, 12-year-old, neutered female, Russian Blue cat. Radiographs revealed bilateral calcified proliferations in the elbow, costochondral and sternochondral joints, which distorted the normal skeletal structure.
View Article and Find Full Text PDFAdv Exp Med Biol
July 2023
Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
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