Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association

Primary hyperparathyroidism (PHP) with pheochromocytoma and neurofibromatosis type 1 is a rare clinical association. We present a case of PHP and pheochromocytoma occurring in a 33-year-old male with familial cutaneous neurofibromatosis.

Detalles Bibliográficos
Autores principales: Behera, Kishore Kumar, Nanaiah, Amrit, Gupta, Ashumi, Rajaratnam, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3683222/
https://www.ncbi.nlm.nih.gov/pubmed/23776920
http://dx.doi.org/10.4103/2230-8210.109670
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author Behera, Kishore Kumar
Nanaiah, Amrit
Gupta, Ashumi
Rajaratnam, Simon
author_facet Behera, Kishore Kumar
Nanaiah, Amrit
Gupta, Ashumi
Rajaratnam, Simon
author_sort Behera, Kishore Kumar
collection PubMed
description Primary hyperparathyroidism (PHP) with pheochromocytoma and neurofibromatosis type 1 is a rare clinical association. We present a case of PHP and pheochromocytoma occurring in a 33-year-old male with familial cutaneous neurofibromatosis.
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spelling pubmed-36832222013-06-17 Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association Behera, Kishore Kumar Nanaiah, Amrit Gupta, Ashumi Rajaratnam, Simon Indian J Endocrinol Metab Case Report Primary hyperparathyroidism (PHP) with pheochromocytoma and neurofibromatosis type 1 is a rare clinical association. We present a case of PHP and pheochromocytoma occurring in a 33-year-old male with familial cutaneous neurofibromatosis. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3683222/ /pubmed/23776920 http://dx.doi.org/10.4103/2230-8210.109670 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
Behera, Kishore Kumar
Nanaiah, Amrit
Gupta, Ashumi
Rajaratnam, Simon
Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association
title Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association
title_full Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association
title_fullStr Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association
title_full_unstemmed Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association
title_short Neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: A rare association
title_sort neurofibromatosis type 1, pheochromocytoma with primary hyperparathyroidism: a rare association
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3683222/
https://www.ncbi.nlm.nih.gov/pubmed/23776920
http://dx.doi.org/10.4103/2230-8210.109670
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AT guptaashumi neurofibromatosistype1pheochromocytomawithprimaryhyperparathyroidismarareassociation
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