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Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma

Tumor-induced osteomalacia (TIO) is a rare, paraneoplastic disorder of hypophosphatemia associated with elevated tumor-produced fibroblast growth factor 23 (FGF23). Maxillofacial tumors are rarely involved in TIO, especially maxillary TIO in children. We present a 14-year-old boy with osteomalacia a...

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Autores principales: Thi, Ha Nguyen, Manh, Cuong Pham, Tuan, Linh To, Le Thi, Lan Anh, Thanh, Nam Nguyen, Vilaiyuk, Soamarat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683546/
https://www.ncbi.nlm.nih.gov/pubmed/35135186
http://dx.doi.org/10.4274/jcrpe.galenos.2022.2021-8-14
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author Thi, Ha Nguyen
Manh, Cuong Pham
Tuan, Linh To
Le Thi, Lan Anh
Thanh, Nam Nguyen
Vilaiyuk, Soamarat
author_facet Thi, Ha Nguyen
Manh, Cuong Pham
Tuan, Linh To
Le Thi, Lan Anh
Thanh, Nam Nguyen
Vilaiyuk, Soamarat
author_sort Thi, Ha Nguyen
collection PubMed
description Tumor-induced osteomalacia (TIO) is a rare, paraneoplastic disorder of hypophosphatemia associated with elevated tumor-produced fibroblast growth factor 23 (FGF23). Maxillofacial tumors are rarely involved in TIO, especially maxillary TIO in children. We present a 14-year-old boy with osteomalacia and high serum levels of FGF23, a hormone associated with decreased phosphate resorption, due to a maxillary tumor. The patient was treated with oral phosphorus and calcitriol, and surgical removal of the tumor was performed. After 21 months follow-up, he was pain free and had returned to full activity. We review the reported pediatric cases of TIO in the maxillofacial and oral region and discuss the management of these patients considering the published evidence.
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spelling pubmed-106835462023-12-01 Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma Thi, Ha Nguyen Manh, Cuong Pham Tuan, Linh To Le Thi, Lan Anh Thanh, Nam Nguyen Vilaiyuk, Soamarat J Clin Res Pediatr Endocrinol Case Report Tumor-induced osteomalacia (TIO) is a rare, paraneoplastic disorder of hypophosphatemia associated with elevated tumor-produced fibroblast growth factor 23 (FGF23). Maxillofacial tumors are rarely involved in TIO, especially maxillary TIO in children. We present a 14-year-old boy with osteomalacia and high serum levels of FGF23, a hormone associated with decreased phosphate resorption, due to a maxillary tumor. The patient was treated with oral phosphorus and calcitriol, and surgical removal of the tumor was performed. After 21 months follow-up, he was pain free and had returned to full activity. We review the reported pediatric cases of TIO in the maxillofacial and oral region and discuss the management of these patients considering the published evidence. Galenos Publishing 2023-12 2023-11-22 /pmc/articles/PMC10683546/ /pubmed/35135186 http://dx.doi.org/10.4274/jcrpe.galenos.2022.2021-8-14 Text en ©Copyright 2023 by Turkish Pediatric Endocrinology and Diabetes Society | The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House. https://creativecommons.org/licenses/by-nc-nd/4.0/Licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 (CC BY-NC-ND) International License.
spellingShingle Case Report
Thi, Ha Nguyen
Manh, Cuong Pham
Tuan, Linh To
Le Thi, Lan Anh
Thanh, Nam Nguyen
Vilaiyuk, Soamarat
Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
title Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
title_full Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
title_fullStr Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
title_full_unstemmed Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
title_short Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
title_sort tumor-induced osteomalacia in a boy with maxillary ossifying fibroma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683546/
https://www.ncbi.nlm.nih.gov/pubmed/35135186
http://dx.doi.org/10.4274/jcrpe.galenos.2022.2021-8-14
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