Letter to the Editor

MEDICATION-RELATED OSTEONECROSIS OF JAW

K. Chatterjee1, A. Banerjee2 , S. Khan3, R. Franco4, H. Uzunçıbuk5 ORCID, G. Cervino6, G. Minervini7

1 Department of Oral and Maxillofacial Pathology, Awadh Dental College and Hospital, Jamshedpur, India
2 Department of Oral and Maxillofacial Pathology, Awadh Dental College and Hospital, Jamshedpur
3 Department of Oral Pathology, KGF College Of Dental Sciences And Hospital, Karnataka, India
4 Department of Biomedicine and Prevention, the University of Rome Tor Vergata, Rome, Italy
5 Department of Orthodontics, Faculty of Dentistry, Trakya University, Edirne, Turkey
6 Dental Sciences and Morphofunctional Imaging, University of Messina, Policlinico “Gaetano Martino”, Messina, Italy
7 Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, Tamil Nadu, India

Correspondence to:

Abhishek Banerjee, MD
Department of Oral and maxillofacial pathology,
Awadh Dental College and Hospital,
NH-33, Danga, P.O. Bhilaipahar, Jamshedpur,
Jharkhand 831012, India
e-mail: abhishek.banerjee376@gmail.com

Annals of Stomatology 2024 May-August 4(2): 83-86
DOI https://doi.org/10.69129/stomatol/2024v4iss2_1


Received: 28 June 2024 Accepted: 2 August 2024


Copyright © by LAB srl 2024 ISSN 2975-1276
This publication and/or article is for individual use only and may not be further reproduced without written permission from the copyright holder. Unauthorized reproduction may result in financial and other penalties. Disclosure: All authors report no conflicts of interest relevant to this article.

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Abstract

Medication-related osteonecrosis of the jaws (MRONJ) primarily occurs as a complication of bone antiresorptive treatment in specific bone treatment modalities. It was first identified in 2003 as a bisphosphonate (BP) treatment complication. Denosumab is a molecule with a particular mode of action. This molecule inhibits bone resorption by suppressing osteoclast function. BPs have a strong affinity for hydroxyapatite crystals and remain in bone for years. The pathogenesis of MRONJ is not fully explained and appears multifactorial.

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