Normocalcemic primary hyperparathyroidism

ABSTRACT Normocalcemic primary hyperparathyroidism (PHPT) is a newer phenotype of PHPT defined by elevated PTH concentrations in the setting of normal serum calcium levels. It is increasingly being diagnosed in the setting of evaluation for nephrolithiasis or metabolic bone diseases. It is important to demonstrate that PTH values remain consistently elevated and to measure ionized calcium levels to make the diagnosis. A diagnosis of normocalcemic disease is one of exclusion of secondary forms of hyperparathyroidism, including vitamin D deficiency, renal failure, medications, malabsorption, and hypercalciuria. Lack of rigorous diagnostic criteria and selection bias of the studied populations may explain the different rates of bone and renal complications. The natural history still remains unknown. Caution should be used in recommending surgery, unless clearly indicated. Here we will review the diagnostic features, epidemiology, clinical presentation, natural history, medical and surgical management of normocalcemic PHPT.

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Main Authors: Cusano,Natalie E., Cetani,Filomena
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Endocrinologia e Metabologia 2022
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972022000500666
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spelling oai:scielo:S2359-399720220005006662022-11-30Normocalcemic primary hyperparathyroidismCusano,Natalie E.Cetani,Filomena Hyperparathyroidism osteoporosis nephrolithiasis parathyroid surgery calcium parathyroid hormone ABSTRACT Normocalcemic primary hyperparathyroidism (PHPT) is a newer phenotype of PHPT defined by elevated PTH concentrations in the setting of normal serum calcium levels. It is increasingly being diagnosed in the setting of evaluation for nephrolithiasis or metabolic bone diseases. It is important to demonstrate that PTH values remain consistently elevated and to measure ionized calcium levels to make the diagnosis. A diagnosis of normocalcemic disease is one of exclusion of secondary forms of hyperparathyroidism, including vitamin D deficiency, renal failure, medications, malabsorption, and hypercalciuria. Lack of rigorous diagnostic criteria and selection bias of the studied populations may explain the different rates of bone and renal complications. The natural history still remains unknown. Caution should be used in recommending surgery, unless clearly indicated. Here we will review the diagnostic features, epidemiology, clinical presentation, natural history, medical and surgical management of normocalcemic PHPT.info:eu-repo/semantics/openAccessSociedade Brasileira de Endocrinologia e MetabologiaArchives of Endocrinology and Metabolism v.66 n.5 20222022-10-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972022000500666en10.20945/2359-3997000000556
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language English
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author Cusano,Natalie E.
Cetani,Filomena
spellingShingle Cusano,Natalie E.
Cetani,Filomena
Normocalcemic primary hyperparathyroidism
author_facet Cusano,Natalie E.
Cetani,Filomena
author_sort Cusano,Natalie E.
title Normocalcemic primary hyperparathyroidism
title_short Normocalcemic primary hyperparathyroidism
title_full Normocalcemic primary hyperparathyroidism
title_fullStr Normocalcemic primary hyperparathyroidism
title_full_unstemmed Normocalcemic primary hyperparathyroidism
title_sort normocalcemic primary hyperparathyroidism
description ABSTRACT Normocalcemic primary hyperparathyroidism (PHPT) is a newer phenotype of PHPT defined by elevated PTH concentrations in the setting of normal serum calcium levels. It is increasingly being diagnosed in the setting of evaluation for nephrolithiasis or metabolic bone diseases. It is important to demonstrate that PTH values remain consistently elevated and to measure ionized calcium levels to make the diagnosis. A diagnosis of normocalcemic disease is one of exclusion of secondary forms of hyperparathyroidism, including vitamin D deficiency, renal failure, medications, malabsorption, and hypercalciuria. Lack of rigorous diagnostic criteria and selection bias of the studied populations may explain the different rates of bone and renal complications. The natural history still remains unknown. Caution should be used in recommending surgery, unless clearly indicated. Here we will review the diagnostic features, epidemiology, clinical presentation, natural history, medical and surgical management of normocalcemic PHPT.
publisher Sociedade Brasileira de Endocrinologia e Metabologia
publishDate 2022
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972022000500666
work_keys_str_mv AT cusanonataliee normocalcemicprimaryhyperparathyroidism
AT cetanifilomena normocalcemicprimaryhyperparathyroidism
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