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A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor
Primary hyperparathyroidism is an endocrinopathy which is characterized with the hypersecretion of parathormone. During the progress of the disease bone loss takes place due to resorption on the subperiosteal and endosteal surfaces. Brown tumor is a localized form of osteitis fibrosa cystica, being...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522506/ https://www.ncbi.nlm.nih.gov/pubmed/23251174 http://dx.doi.org/10.1155/2012/432676 |
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author | Mantar, F. Gunduz, S. Gunduz, U. R. |
author_facet | Mantar, F. Gunduz, S. Gunduz, U. R. |
author_sort | Mantar, F. |
collection | PubMed |
description | Primary hyperparathyroidism is an endocrinopathy which is characterized with the hypersecretion of parathormone. During the progress of the disease bone loss takes place due to resorption on the subperiosteal and endosteal surfaces. Brown tumor is a localized form of osteitis fibrosa cystica, being part of the hyperparathyroid bone disease. It is rarely the first symptom of hyperparathyroidism. Nowadays, the diagnosis is made at an asymptomatic or minimally symptomatic stage. We present a male patient presented with a massive painless swelling in the left maxilla as the first manifestation of primary hyperparathyroidism due to a parathyroid adenoma. Parathyroidectomy was performed, and there was a regression of the bone lesion, without the need of performing other local surgical procedures. |
format | Online Article Text |
id | pubmed-3522506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35225062012-12-18 A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor Mantar, F. Gunduz, S. Gunduz, U. R. Case Rep Med Case Report Primary hyperparathyroidism is an endocrinopathy which is characterized with the hypersecretion of parathormone. During the progress of the disease bone loss takes place due to resorption on the subperiosteal and endosteal surfaces. Brown tumor is a localized form of osteitis fibrosa cystica, being part of the hyperparathyroid bone disease. It is rarely the first symptom of hyperparathyroidism. Nowadays, the diagnosis is made at an asymptomatic or minimally symptomatic stage. We present a male patient presented with a massive painless swelling in the left maxilla as the first manifestation of primary hyperparathyroidism due to a parathyroid adenoma. Parathyroidectomy was performed, and there was a regression of the bone lesion, without the need of performing other local surgical procedures. Hindawi Publishing Corporation 2012 2012-11-21 /pmc/articles/PMC3522506/ /pubmed/23251174 http://dx.doi.org/10.1155/2012/432676 Text en Copyright © 2012 F. Mantar et al. https://creativecommons.org/licenses/by/3.0/ 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 Mantar, F. Gunduz, S. Gunduz, U. R. A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor |
title | A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor |
title_full | A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor |
title_fullStr | A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor |
title_full_unstemmed | A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor |
title_short | A Reference Finding Rarely Seen in Primary Hyperparathyroidism: Brown Tumor |
title_sort | reference finding rarely seen in primary hyperparathyroidism: brown tumor |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522506/ https://www.ncbi.nlm.nih.gov/pubmed/23251174 http://dx.doi.org/10.1155/2012/432676 |
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