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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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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. |
format | Online Article Text |
id | pubmed-3354855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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