AccScience Publishing / TD / Volume 3 / Issue 1 / DOI: 10.36922/td.2096
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CASE REPORT

Odontogenic myxofibroma arising in the mandibular angle of a child with long-term follow-up: A case report

Momoko Yoshikawa1,2 ,  Takeshi Karube1 ,  Hiroki Nagamine1 ,  Wataru Muraoka1,3 ,  Hideki Kizu1,4 ,  Hiromasa Kawana1,5 ,  Taneaki Nakagawa1 ,  Seiji Asoda1*
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1 Department of Dentistry and Oral Surgery, School of Medicine, Keio University, Tokyo, Japan
2 Department of Dentistry and Oral Surgery, National Hospital Organization, Murayama Medical Center, Tokyo, Japan
3 Department of Dentistry and Oral Surgery, Kawasaki Municipal Ida Hospital, Kawasaki, Japan
4 Department of Dentistry and Oral Surgery, Federation of National Public Service Personnel Mutual Aid Associations, Tachikawa Hospital, Tokyo, Japan
5 Department of Oral and Maxillofacial Implantology, Kanagawa Dental University, Yokosuka, Japan
Tumor Discovery 2024, 3(1), 2096 https://doi.org/10.36922/td.2096
Submitted: 24 October 2023 | Accepted: 11 January 2024 | Published: 19 March 2024
© 2024 by the Author (s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
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Abstract

Odontogenic myxofibroma of the jawbone is a rarity in children, and there are few reports of cases with long-term follow-up, which mainly describe the growth process of odontogenic myxofibroma. We herein report a case of odontogenic myxofibroma that arose in the mandibular angle of a pediatric patient with a long-term follow-up of more than 14 years. The patient, when he was 10-years-old, first approached us with a complaint of painless swelling in the right mandibular angle that was palpable and showed bone-like hardness. Computed tomography revealed an ill-defined bone defect measuring 20 mm in diameter with bone protrusion in the margin. A biopsy was performed to differentiate the mass from osteosarcoma, giving a preliminary diagnosis of odontogenic myxofibroma or chondromyxofibroma. Therefore, tumorectomy was performed under general anesthesia. We curetted the bone surrounding the tumor and filled defect with iliac cancellous bone. The final diagnosis was odontogenic myxofibroma. At present, 14 years after the surgery, the patient had experienced an uneventful post-operative course without recurrence.

Keywords
Odontogenic myxofibroma
Pediatric tumor
Long-term follow-up
Funding
None.
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Conflict of interest
The authors declare no conflict of interests.
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Tumor Discovery, Electronic ISSN: 2810-9775 Published by AccScience Publishing
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