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Current Understanding and Management of Parathyroid Carcinoma

Received: 30 March 2017    Accepted: 19 April 2017    Published: 31 May 2017
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Abstract

Parathyroid adenomas are a very common endocrine entity, whereas parathyroid carcinomas (PC) are extremely rare. With an estimated incidence of 0.015 per 100,000 population and an estimated prevalence of 0.005% in the United States, parathyroid cancer is one of the rarest of all human malignancies. PC is an extremely rare cause of primary hyperparathyroidism (PHPT). Men and women are equally affected, usually in the fourth or fifth decade of life. The exact etiology has not been identified, but mutations in the CDC73 gene appear to have a critical role in its pathogenesis. The morbidity and mortality of PC is secondary to the hypercalcemia resulting from tumor overproduction of PTH. The primary management objectives are complete removal of the cancer and prevention of recurrences. This review will talk about the epidemiology, etiology, clinical manifestations, and management of PC.

Published in Journal of Cancer Treatment and Research (Volume 5, Issue 3)
DOI 10.11648/j.jctr.20170503.15
Page(s) 51-61
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Parathyroid Cancer, Hyperparathyroidism, Hypercalcemia, Parathyroid Carcinoma

References
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    Rodrigo Arrangoiz, Fernando Cordera, David Caba, Manuel Muñoz Juarez, Eduardo Moreno, et al. (2017). Current Understanding and Management of Parathyroid Carcinoma. Journal of Cancer Treatment and Research, 5(3), 51-61. https://doi.org/10.11648/j.jctr.20170503.15

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    Rodrigo Arrangoiz; Fernando Cordera; David Caba; Manuel Muñoz Juarez; Eduardo Moreno, et al. Current Understanding and Management of Parathyroid Carcinoma. J. Cancer Treat. Res. 2017, 5(3), 51-61. doi: 10.11648/j.jctr.20170503.15

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    AMA Style

    Rodrigo Arrangoiz, Fernando Cordera, David Caba, Manuel Muñoz Juarez, Eduardo Moreno, et al. Current Understanding and Management of Parathyroid Carcinoma. J Cancer Treat Res. 2017;5(3):51-61. doi: 10.11648/j.jctr.20170503.15

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  • @article{10.11648/j.jctr.20170503.15,
      author = {Rodrigo Arrangoiz and Fernando Cordera and David Caba and Manuel Muñoz Juarez and Eduardo Moreno and Enrique Luque de Leon},
      title = {Current Understanding and Management of Parathyroid Carcinoma},
      journal = {Journal of Cancer Treatment and Research},
      volume = {5},
      number = {3},
      pages = {51-61},
      doi = {10.11648/j.jctr.20170503.15},
      url = {https://doi.org/10.11648/j.jctr.20170503.15},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jctr.20170503.15},
      abstract = {Parathyroid adenomas are a very common endocrine entity, whereas parathyroid carcinomas (PC) are extremely rare. With an estimated incidence of 0.015 per 100,000 population and an estimated prevalence of 0.005% in the United States, parathyroid cancer is one of the rarest of all human malignancies. PC is an extremely rare cause of primary hyperparathyroidism (PHPT). Men and women are equally affected, usually in the fourth or fifth decade of life. The exact etiology has not been identified, but mutations in the CDC73 gene appear to have a critical role in its pathogenesis. The morbidity and mortality of PC is secondary to the hypercalcemia resulting from tumor overproduction of PTH. The primary management objectives are complete removal of the cancer and prevention of recurrences. This review will talk about the epidemiology, etiology, clinical manifestations, and management of PC.},
     year = {2017}
    }
    

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    AU  - Rodrigo Arrangoiz
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    AU  - David Caba
    AU  - Manuel Muñoz Juarez
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    AB  - Parathyroid adenomas are a very common endocrine entity, whereas parathyroid carcinomas (PC) are extremely rare. With an estimated incidence of 0.015 per 100,000 population and an estimated prevalence of 0.005% in the United States, parathyroid cancer is one of the rarest of all human malignancies. PC is an extremely rare cause of primary hyperparathyroidism (PHPT). Men and women are equally affected, usually in the fourth or fifth decade of life. The exact etiology has not been identified, but mutations in the CDC73 gene appear to have a critical role in its pathogenesis. The morbidity and mortality of PC is secondary to the hypercalcemia resulting from tumor overproduction of PTH. The primary management objectives are complete removal of the cancer and prevention of recurrences. This review will talk about the epidemiology, etiology, clinical manifestations, and management of PC.
    VL  - 5
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Author Information
  • Department of Surgical Oncology, American British Cowdray Medical Center, Mexico City, Mexico

  • Department of Surgical Oncology, American British Cowdray Medical Center, Mexico City, Mexico

  • Department of Surgical Oncology, American British Cowdray Medical Center, Mexico City, Mexico

  • Department of Surgical Oncology, American British Cowdray Medical Center, Mexico City, Mexico

  • Department of Surgical Oncology, American British Cowdray Medical Center, Mexico City, Mexico

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