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Childhood adrenocortical carcinoma: Case report and review

Adrenocortical cancers in childhood are very rare tumors. The tumors have varied presentation — either virilizing forms or presentation with Cushing's syndrome, or both. In children, due to the rapid development of symptoms they come to attention early, however, if not diagnosed and treated ear...

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Autores principales: Gundgurthi, Abhay, Kharb, Sandeep, Dutta, Manoj K., Garg, M. K., Khare, Abhisek, Jacob, M. Joseph, Bhardwaj, Reena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354855/
https://www.ncbi.nlm.nih.gov/pubmed/22629514
http://dx.doi.org/10.4103/2230-8210.95699
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author Gundgurthi, Abhay
Kharb, Sandeep
Dutta, Manoj K.
Garg, M. K.
Khare, Abhisek
Jacob, M. Joseph
Bhardwaj, Reena
author_facet Gundgurthi, Abhay
Kharb, Sandeep
Dutta, Manoj K.
Garg, M. K.
Khare, Abhisek
Jacob, M. Joseph
Bhardwaj, Reena
author_sort Gundgurthi, Abhay
collection PubMed
description Adrenocortical cancers in childhood are very rare tumors. The tumors have varied presentation — either virilizing forms or presentation with Cushing's syndrome, or both. In children, due to the rapid development of symptoms they come to attention early, however, if not diagnosed and treated early can have a downhill course. The last decade has seen the emergence of new diagnostic imaging modalities. There is also intense ongoing research in newer treatment modalities as these tumors can be unresectable or have a high recurrence rate.
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spelling pubmed-33548552012-05-24 Childhood adrenocortical carcinoma: Case report and review Gundgurthi, Abhay Kharb, Sandeep Dutta, Manoj K. Garg, M. K. Khare, Abhisek Jacob, M. Joseph Bhardwaj, Reena Indian J Endocrinol Metab Case-Based Review of Literature Adrenocortical cancers in childhood are very rare tumors. The tumors have varied presentation — either virilizing forms or presentation with Cushing's syndrome, or both. In children, due to the rapid development of symptoms they come to attention early, however, if not diagnosed and treated early can have a downhill course. The last decade has seen the emergence of new diagnostic imaging modalities. There is also intense ongoing research in newer treatment modalities as these tumors can be unresectable or have a high recurrence rate. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3354855/ /pubmed/22629514 http://dx.doi.org/10.4103/2230-8210.95699 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-Based Review of Literature
Gundgurthi, Abhay
Kharb, Sandeep
Dutta, Manoj K.
Garg, M. K.
Khare, Abhisek
Jacob, M. Joseph
Bhardwaj, Reena
Childhood adrenocortical carcinoma: Case report and review
title Childhood adrenocortical carcinoma: Case report and review
title_full Childhood adrenocortical carcinoma: Case report and review
title_fullStr Childhood adrenocortical carcinoma: Case report and review
title_full_unstemmed Childhood adrenocortical carcinoma: Case report and review
title_short Childhood adrenocortical carcinoma: Case report and review
title_sort childhood adrenocortical carcinoma: case report and review
topic Case-Based Review of Literature
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354855/
https://www.ncbi.nlm.nih.gov/pubmed/22629514
http://dx.doi.org/10.4103/2230-8210.95699
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