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Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy

Primary hyperparathyroidism is a disease characterized by excessive secretion of parathormone. During the course of this disease, bone loss occurs, particularly depending on resorption of the skeletal system. One of the complications of primary hyperparathyroidism is fibrotic, cystic bony changes wh...

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Autores principales: Ullah, Ekram, Ahmad, Mehtab, Ali, Syed Asmat, Redhu, Navneet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510937/
https://www.ncbi.nlm.nih.gov/pubmed/23226663
http://dx.doi.org/10.4103/2230-8210.103037
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author Ullah, Ekram
Ahmad, Mehtab
Ali, Syed Asmat
Redhu, Navneet
author_facet Ullah, Ekram
Ahmad, Mehtab
Ali, Syed Asmat
Redhu, Navneet
author_sort Ullah, Ekram
collection PubMed
description Primary hyperparathyroidism is a disease characterized by excessive secretion of parathormone. During the course of this disease, bone loss occurs, particularly depending on resorption of the skeletal system. One of the complications of primary hyperparathyroidism is fibrotic, cystic bony changes which is called Brown tumor. Skeletal manifestations in the form of Brown tumors are rare and according to literature occur in less than 2% of patients suffering from any form of hyperparathyroidism. Such rare and multiple benign lesions may simulate a malignant neoplasm and pose a real challenge for the clinician in its differential diagnosis. We present a case of a 23-year-old Indian woman who was evaluated for multiple lytic expansile lesions with a strong suspicion of malignancy and fibrous dysplasia but turned out to be a case of primary hyperparathyroidism.
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spelling pubmed-35109372012-12-05 Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy Ullah, Ekram Ahmad, Mehtab Ali, Syed Asmat Redhu, Navneet Indian J Endocrinol Metab Case Report Primary hyperparathyroidism is a disease characterized by excessive secretion of parathormone. During the course of this disease, bone loss occurs, particularly depending on resorption of the skeletal system. One of the complications of primary hyperparathyroidism is fibrotic, cystic bony changes which is called Brown tumor. Skeletal manifestations in the form of Brown tumors are rare and according to literature occur in less than 2% of patients suffering from any form of hyperparathyroidism. Such rare and multiple benign lesions may simulate a malignant neoplasm and pose a real challenge for the clinician in its differential diagnosis. We present a case of a 23-year-old Indian woman who was evaluated for multiple lytic expansile lesions with a strong suspicion of malignancy and fibrous dysplasia but turned out to be a case of primary hyperparathyroidism. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3510937/ /pubmed/23226663 http://dx.doi.org/10.4103/2230-8210.103037 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ullah, Ekram
Ahmad, Mehtab
Ali, Syed Asmat
Redhu, Navneet
Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy
title Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy
title_full Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy
title_fullStr Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy
title_full_unstemmed Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy
title_short Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy
title_sort primary hyperparathyroidism having multiple brown tumors mimicking malignancy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510937/
https://www.ncbi.nlm.nih.gov/pubmed/23226663
http://dx.doi.org/10.4103/2230-8210.103037
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