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Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report

The existence of normocalcemic primary hyperparathyroidism (NPHP) was acknowledged at the Third and Fourth International Proceedings on primary hyperparathyroidism PHPT but data relating to its clinical presentation, natural history, and skeletal status were limited and there was no information nor...

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Autor principal: Tucci, Joseph R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736859/
https://www.ncbi.nlm.nih.gov/pubmed/29276732
http://dx.doi.org/10.1016/j.bonr.2017.10.001
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author Tucci, Joseph R.
author_facet Tucci, Joseph R.
author_sort Tucci, Joseph R.
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description The existence of normocalcemic primary hyperparathyroidism (NPHP) was acknowledged at the Third and Fourth International Proceedings on primary hyperparathyroidism PHPT but data relating to its clinical presentation, natural history, and skeletal status were limited and there was no information nor guidelines as to definitive therapy. Herein are reported biochemical, hormonal, and densitometry data in a postmenopausal woman seen initially for osteoporosis who was found to have increased serum PTH levels and normal serum total and ionized calcium levels without evidence of secondary hyperparathyroidism. Over a seven year period, the patient exhibited continuing preferential cortical bone loss at the one-third site of the radius in the face of relatively stable readings at the lumbar spine and hip that led to a subtotal parathyroidectomy for parathyroid hyperplasia with resultant normalization of serum PTH.
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spelling pubmed-57368592017-12-22 Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report Tucci, Joseph R. Bone Rep Article The existence of normocalcemic primary hyperparathyroidism (NPHP) was acknowledged at the Third and Fourth International Proceedings on primary hyperparathyroidism PHPT but data relating to its clinical presentation, natural history, and skeletal status were limited and there was no information nor guidelines as to definitive therapy. Herein are reported biochemical, hormonal, and densitometry data in a postmenopausal woman seen initially for osteoporosis who was found to have increased serum PTH levels and normal serum total and ionized calcium levels without evidence of secondary hyperparathyroidism. Over a seven year period, the patient exhibited continuing preferential cortical bone loss at the one-third site of the radius in the face of relatively stable readings at the lumbar spine and hip that led to a subtotal parathyroidectomy for parathyroid hyperplasia with resultant normalization of serum PTH. Elsevier 2017-10-10 /pmc/articles/PMC5736859/ /pubmed/29276732 http://dx.doi.org/10.1016/j.bonr.2017.10.001 Text en © 2017 The Author http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Tucci, Joseph R.
Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report
title Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report
title_full Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report
title_fullStr Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report
title_full_unstemmed Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report
title_short Normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – A case report
title_sort normocalcemic primary hyperparathyroidism associated with progressive cortical bone loss – a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736859/
https://www.ncbi.nlm.nih.gov/pubmed/29276732
http://dx.doi.org/10.1016/j.bonr.2017.10.001
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