Cargando…
Primary Ewing’s Sarcoma of the temporal bone in an infant
Introduction : Ewing’s sarcoma is the second most common primary malignant tumor of bone found in children after Osteosarcoma. It accounts for 4–9% of primary malignant bone tumors and it affects bones of the skull or face in only 1–4% of cases. Hence it rarely affects the head and neck. Subject and...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410288/ https://www.ncbi.nlm.nih.gov/pubmed/25922651 |
_version_ | 1782368304114958336 |
---|---|
author | Goudarzipour, Kourosh Shamsian, Shahin Alavi, Samin Nourbakhsh, Kazem Aghakhani, Roxana Eydian, Zahra Arzanian, Mohammad Taghi |
author_facet | Goudarzipour, Kourosh Shamsian, Shahin Alavi, Samin Nourbakhsh, Kazem Aghakhani, Roxana Eydian, Zahra Arzanian, Mohammad Taghi |
author_sort | Goudarzipour, Kourosh |
collection | PubMed |
description | Introduction : Ewing’s sarcoma is the second most common primary malignant tumor of bone found in children after Osteosarcoma. It accounts for 4–9% of primary malignant bone tumors and it affects bones of the skull or face in only 1–4% of cases. Hence it rarely affects the head and neck. Subject and Method : In this case report, we describe a case of primary Ewing's sarcoma occurring in the temporal bone. The tumor was surgically excised, and the patient underwent chemotherapy for ten months. Results : Neither recurrence nor distant metastasis was noted in these 10 months after surgery but about 18 months after surgery our patient was expired. Conclusion : Although the prognosis of Ewing's sarcoma is generally poor because of early metastasis to the lungs and to other bones, a review of the article suggested that Ewing’s sarcoma occurring in the skull can often be successfully managed by intensive therapy with radical excision and chemotherapy. This result was supported by the case reported here. |
format | Online Article Text |
id | pubmed-4410288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center |
record_format | MEDLINE/PubMed |
spelling | pubmed-44102882015-04-28 Primary Ewing’s Sarcoma of the temporal bone in an infant Goudarzipour, Kourosh Shamsian, Shahin Alavi, Samin Nourbakhsh, Kazem Aghakhani, Roxana Eydian, Zahra Arzanian, Mohammad Taghi Int J Hematol Oncol Stem Cell Res Case Report Introduction : Ewing’s sarcoma is the second most common primary malignant tumor of bone found in children after Osteosarcoma. It accounts for 4–9% of primary malignant bone tumors and it affects bones of the skull or face in only 1–4% of cases. Hence it rarely affects the head and neck. Subject and Method : In this case report, we describe a case of primary Ewing's sarcoma occurring in the temporal bone. The tumor was surgically excised, and the patient underwent chemotherapy for ten months. Results : Neither recurrence nor distant metastasis was noted in these 10 months after surgery but about 18 months after surgery our patient was expired. Conclusion : Although the prognosis of Ewing's sarcoma is generally poor because of early metastasis to the lungs and to other bones, a review of the article suggested that Ewing’s sarcoma occurring in the skull can often be successfully managed by intensive therapy with radical excision and chemotherapy. This result was supported by the case reported here. Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2015-04-01 /pmc/articles/PMC4410288/ /pubmed/25922651 Text en Copyright : © International Journal of Hematology-Oncology and Stem Cell Research & Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Goudarzipour, Kourosh Shamsian, Shahin Alavi, Samin Nourbakhsh, Kazem Aghakhani, Roxana Eydian, Zahra Arzanian, Mohammad Taghi Primary Ewing’s Sarcoma of the temporal bone in an infant |
title | Primary Ewing’s Sarcoma of the temporal bone in an infant |
title_full | Primary Ewing’s Sarcoma of the temporal bone in an infant |
title_fullStr | Primary Ewing’s Sarcoma of the temporal bone in an infant |
title_full_unstemmed | Primary Ewing’s Sarcoma of the temporal bone in an infant |
title_short | Primary Ewing’s Sarcoma of the temporal bone in an infant |
title_sort | primary ewing’s sarcoma of the temporal bone in an infant |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410288/ https://www.ncbi.nlm.nih.gov/pubmed/25922651 |
work_keys_str_mv | AT goudarzipourkourosh primaryewingssarcomaofthetemporalboneinaninfant AT shamsianshahin primaryewingssarcomaofthetemporalboneinaninfant AT alavisamin primaryewingssarcomaofthetemporalboneinaninfant AT nourbakhshkazem primaryewingssarcomaofthetemporalboneinaninfant AT aghakhaniroxana primaryewingssarcomaofthetemporalboneinaninfant AT eydianzahra primaryewingssarcomaofthetemporalboneinaninfant AT arzanianmohammadtaghi primaryewingssarcomaofthetemporalboneinaninfant |