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Osteosarcoma and its Association with Chromosomal Abnormalities | OMICS International| Abstract
ISSN 2472-016X

Journal of Orthopedic Oncology
Open Access

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  • Review Article   
  • J Orthop Oncol 2022, Vol 8(4): 174
  • DOI: 10.4172/2472-016X.1000174

Osteosarcoma and its Association with Chromosomal Abnormalities

Katalin Borbely*
Department of Medicine, Medical University of Pecs and Kaposvar, Hungary
*Corresponding Author : Katalin Borbely, Department of Medicine, Medical University of Pecs and Kaposvar, Hungary, Email: katalin.b@gmail.com

Received Date: Jun 28, 2022 / Published Date: Jul 30, 2022

Abstract

Osteosarcoma is the most common non-hematological malignant bone disease in children and adults. The peak incidence occurs in the first 10 years and gradually decreases after the age of 50. Osteosarcoma usually occurs around the growth plate of long bones. Most osteosarcoma tumors are of high grade and are prone to develop lung metastases. Despite clinical improvement, patients with metastatic or recurrent disease have a poor prognosis. Here we review the current understanding of human osteosarcoma, focusing on the clinical aspects and chromosomal abnormalities. With the rapid expansion of knowledge of stem cell biology, it is new that osteosarcoma should be regarded as a differentiation disease caused by genetic and metamorphic changes that interfere with the differentiation of osteoblasts from mesenchymal stem cells.

Citation: Borbély K (2022) Osteosarcoma and its Association with Chromosomal Abnormalities. J Orthop Oncol 8: 174. Doi: 10.4172/2472-016X.1000174

Copyright: © 2022 Borbely K. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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