Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3

Familial hypocalciuric hypercalcemia type 3 should be considered as differential diagnosis in patients with suspected primary hyperparathyroidism and/or suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for going through multiple futile parathyroidectomies and for t...

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Autores principales: Hovden, Silje, Jespersen, Marie Louise, Nissen, Peter H., Poulsen, Per Løgstrup, Rolighed, Lars, Ladefoged, Søren A., Rejnmark, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054464/
https://www.ncbi.nlm.nih.gov/pubmed/27761240
http://dx.doi.org/10.1002/ccr3.657
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author Hovden, Silje
Jespersen, Marie Louise
Nissen, Peter H.
Poulsen, Per Løgstrup
Rolighed, Lars
Ladefoged, Søren A.
Rejnmark, Lars
author_facet Hovden, Silje
Jespersen, Marie Louise
Nissen, Peter H.
Poulsen, Per Løgstrup
Rolighed, Lars
Ladefoged, Søren A.
Rejnmark, Lars
author_sort Hovden, Silje
collection PubMed
description Familial hypocalciuric hypercalcemia type 3 should be considered as differential diagnosis in patients with suspected primary hyperparathyroidism and/or suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for going through multiple futile parathyroidectomies and for the worry of being diagnosed with a cancer susceptibility syndrome.
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spelling pubmed-50544642016-10-19 Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3 Hovden, Silje Jespersen, Marie Louise Nissen, Peter H. Poulsen, Per Løgstrup Rolighed, Lars Ladefoged, Søren A. Rejnmark, Lars Clin Case Rep Case Reports Familial hypocalciuric hypercalcemia type 3 should be considered as differential diagnosis in patients with suspected primary hyperparathyroidism and/or suspected multiple neoplasia syndrome, as correct diagnosis will spare the patients for going through multiple futile parathyroidectomies and for the worry of being diagnosed with a cancer susceptibility syndrome. John Wiley and Sons Inc. 2016-08-18 /pmc/articles/PMC5054464/ /pubmed/27761240 http://dx.doi.org/10.1002/ccr3.657 Text en © 2016 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Hovden, Silje
Jespersen, Marie Louise
Nissen, Peter H.
Poulsen, Per Løgstrup
Rolighed, Lars
Ladefoged, Søren A.
Rejnmark, Lars
Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
title Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
title_full Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
title_fullStr Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
title_full_unstemmed Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
title_short Multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
title_sort multiple endocrine neoplasia phenocopy revealed as a co‐occurring neuroendocrine tumor and familial hypocalciuric hypercalcemia type 3
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054464/
https://www.ncbi.nlm.nih.gov/pubmed/27761240
http://dx.doi.org/10.1002/ccr3.657
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