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Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
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Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during...
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Bone formation, or ossification, begins around the sixth to seventh week of embryonic development. Most bones develop from a cartilaginous template through the process of endochondral ossification. Cartilage formation begins when clusters of mesenchymal cells differentiate into chondrocytes. These chondrocytes proliferate rapidly and secrete an extracellular matrix that becomes encased in a membrane called the perichondrium. The resulting cartilage model provides a template that resembles the...
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Most bones contain compact and spongy osseous tissue, but their distribution and concentration vary based on the bone's overall function.
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Cervical Osteoma in Hereditary Multiple Exostoses.

Jitender Chaturvedi1, Niraj Kumar2, Jitendra Shakya1

  • 1Department of Neurosurgery, All India Institute of Medical Sciences (AIIMS), Rishikesh, Uttarakhand, India.

Journal of Pediatric Neurosciences
|September 26, 2022
PubMed
Summary

This study details a rare case of hereditary multiple exostoses (HME) in a teenage boy with a cervical spinal tumor causing myelopathy. It highlights the genetic basis and rarity of such spinal osteomas in HME patients.

Area of Science:

  • Orthopedics
  • Genetics
  • Neurology

Background:

Keywords:
Cervicalhereditary multiple exostosismyelopathyosteomaspine

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  • Osteoid osteoma is a benign bone tumor, often affecting long bones in adolescents, with a genetic predisposition.
  • Spinal intracanal osteomas are exceptionally rare, with cervical lesions presenting significant clinical challenges.
  • Hereditary Multiple Exostoses (HME) is a genetic disorder characterized by multiple bone outgrowths, increasing the risk of secondary complications.