Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome

Hyperparathyroidism-jaw tumour (HPT-JT) syndrome is a rare autosomal dominant disease. It is caused by a gene mutation of the tumour suppressor gene CDC73 that encodes for parafibromin. This syndrome predisposes to a triad occurrence of multiple maxillary or mandibular cemento-ossifying fibroma, par...

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Autores principales: Apandi, Nurul Inaas Mahamad, Basri, Nor Nazaliza, Jalil, Ajura Abdul, Jelon, Md Arad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017210/
https://www.ncbi.nlm.nih.gov/pubmed/36937223
http://dx.doi.org/10.1155/2023/4664619
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author Apandi, Nurul Inaas Mahamad
Basri, Nor Nazaliza
Jalil, Ajura Abdul
Jelon, Md Arad
author_facet Apandi, Nurul Inaas Mahamad
Basri, Nor Nazaliza
Jalil, Ajura Abdul
Jelon, Md Arad
author_sort Apandi, Nurul Inaas Mahamad
collection PubMed
description Hyperparathyroidism-jaw tumour (HPT-JT) syndrome is a rare autosomal dominant disease. It is caused by a gene mutation of the tumour suppressor gene CDC73 that encodes for parafibromin. This syndrome predisposes to a triad occurrence of multiple maxillary or mandibular cemento-ossifying fibroma, parathyroid adenoma or carcinoma, and renal and uterine tumours. In this study, we report a case of HPT-JT occurring in a 30-year-old male patient.
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spelling pubmed-100172102023-03-16 Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome Apandi, Nurul Inaas Mahamad Basri, Nor Nazaliza Jalil, Ajura Abdul Jelon, Md Arad Case Rep Dent Case Report Hyperparathyroidism-jaw tumour (HPT-JT) syndrome is a rare autosomal dominant disease. It is caused by a gene mutation of the tumour suppressor gene CDC73 that encodes for parafibromin. This syndrome predisposes to a triad occurrence of multiple maxillary or mandibular cemento-ossifying fibroma, parathyroid adenoma or carcinoma, and renal and uterine tumours. In this study, we report a case of HPT-JT occurring in a 30-year-old male patient. Hindawi 2023-03-08 /pmc/articles/PMC10017210/ /pubmed/36937223 http://dx.doi.org/10.1155/2023/4664619 Text en Copyright © 2023 Nurul Inaas Mahamad Apandi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Apandi, Nurul Inaas Mahamad
Basri, Nor Nazaliza
Jalil, Ajura Abdul
Jelon, Md Arad
Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
title Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
title_full Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
title_fullStr Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
title_full_unstemmed Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
title_short Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
title_sort multiple cemento-ossifying fibroma: a sign of hyperparathyroidism-jaw tumour syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017210/
https://www.ncbi.nlm.nih.gov/pubmed/36937223
http://dx.doi.org/10.1155/2023/4664619
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AT jalilajuraabdul multiplecementoossifyingfibromaasignofhyperparathyroidismjawtumoursyndrome
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