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Ewing’s Sarcoma of the Adrenal Gland
Ewing’s sarcoma (ES) or primitive neuro-ectodermal tumor (PNET) typically occurs in long or flat bones, the chest wall, extra-skeletal soft tissue, and rarely in solid organs. Incidence of adrenal Ewing’s sarcoma is very rare. Here we report a case of Ewing’s sarcoma of the right adrenal gland in an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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EL-MED-Pub
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921217/ https://www.ncbi.nlm.nih.gov/pubmed/27398321 http://dx.doi.org/10.21699/ajcr.v7i3.406 |
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author | Pal, Dilip Kumar Chandra, Vipin Ranjan, Kumar Rajiv Chakrabortty, Debasis Banerjee, Manju |
author_facet | Pal, Dilip Kumar Chandra, Vipin Ranjan, Kumar Rajiv Chakrabortty, Debasis Banerjee, Manju |
author_sort | Pal, Dilip Kumar |
collection | PubMed |
description | Ewing’s sarcoma (ES) or primitive neuro-ectodermal tumor (PNET) typically occurs in long or flat bones, the chest wall, extra-skeletal soft tissue, and rarely in solid organs. Incidence of adrenal Ewing’s sarcoma is very rare. Here we report a case of Ewing’s sarcoma of the right adrenal gland in an 8-year-old girl who presented with an abdominal mass. The huge tumor was managed by preoperative neo-adjuvant chemotherapy followed by surgical resection. She died due to metastasis after five months of surgery. |
format | Online Article Text |
id | pubmed-4921217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | EL-MED-Pub |
record_format | MEDLINE/PubMed |
spelling | pubmed-49212172016-07-09 Ewing’s Sarcoma of the Adrenal Gland Pal, Dilip Kumar Chandra, Vipin Ranjan, Kumar Rajiv Chakrabortty, Debasis Banerjee, Manju APSP J Case Rep Case Report Ewing’s sarcoma (ES) or primitive neuro-ectodermal tumor (PNET) typically occurs in long or flat bones, the chest wall, extra-skeletal soft tissue, and rarely in solid organs. Incidence of adrenal Ewing’s sarcoma is very rare. Here we report a case of Ewing’s sarcoma of the right adrenal gland in an 8-year-old girl who presented with an abdominal mass. The huge tumor was managed by preoperative neo-adjuvant chemotherapy followed by surgical resection. She died due to metastasis after five months of surgery. EL-MED-Pub 2016-06-15 /pmc/articles/PMC4921217/ /pubmed/27398321 http://dx.doi.org/10.21699/ajcr.v7i3.406 Text en Copyright © 2016 AJCR http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Pal, Dilip Kumar Chandra, Vipin Ranjan, Kumar Rajiv Chakrabortty, Debasis Banerjee, Manju Ewing’s Sarcoma of the Adrenal Gland |
title | Ewing’s Sarcoma of the Adrenal Gland |
title_full | Ewing’s Sarcoma of the Adrenal Gland |
title_fullStr | Ewing’s Sarcoma of the Adrenal Gland |
title_full_unstemmed | Ewing’s Sarcoma of the Adrenal Gland |
title_short | Ewing’s Sarcoma of the Adrenal Gland |
title_sort | ewing’s sarcoma of the adrenal gland |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921217/ https://www.ncbi.nlm.nih.gov/pubmed/27398321 http://dx.doi.org/10.21699/ajcr.v7i3.406 |
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