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Sellar and Parasellar Metastatic Tumors

The sellar and parasellar (SPS) region is a complex area rich in vital neurovascular structures and as such may be the location of first manifestation of a systemic malignancy. Metastases to this region are rare; breast cancer is the most common source among those that metastasize to the SPS region....

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Detalles Bibliográficos
Autores principales: Altay, Tamer, Krisht, Khaled M., Couldwell, William T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263702/
https://www.ncbi.nlm.nih.gov/pubmed/22312541
http://dx.doi.org/10.1155/2012/647256
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author Altay, Tamer
Krisht, Khaled M.
Couldwell, William T.
author_facet Altay, Tamer
Krisht, Khaled M.
Couldwell, William T.
author_sort Altay, Tamer
collection PubMed
description The sellar and parasellar (SPS) region is a complex area rich in vital neurovascular structures and as such may be the location of first manifestation of a systemic malignancy. Metastases to this region are rare; breast cancer is the most common source among those that metastasize to the SPS region. Ophthalmoplegia, headache, retroorbital or facial pain, diabetes insipidus, and visual field defects are the most commonly reported symptoms. Lack of specific clinical and radiological features renders SPS metastases difficult to differentiate from the other frequently encountered lesions in this area, especially when there is no known history of a primary disease. Currently accepted management is multimodality therapy that includes biopsy and/or palliative surgical resection, radiation, and chemotherapy. Although no significant survival benefits have been shown by the surgical series, surgical resection may improve quality of life. Here we review the relevant literature and present six illustrative cases from our own institution.
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spelling pubmed-32637022012-02-06 Sellar and Parasellar Metastatic Tumors Altay, Tamer Krisht, Khaled M. Couldwell, William T. Int J Surg Oncol Clinical Study The sellar and parasellar (SPS) region is a complex area rich in vital neurovascular structures and as such may be the location of first manifestation of a systemic malignancy. Metastases to this region are rare; breast cancer is the most common source among those that metastasize to the SPS region. Ophthalmoplegia, headache, retroorbital or facial pain, diabetes insipidus, and visual field defects are the most commonly reported symptoms. Lack of specific clinical and radiological features renders SPS metastases difficult to differentiate from the other frequently encountered lesions in this area, especially when there is no known history of a primary disease. Currently accepted management is multimodality therapy that includes biopsy and/or palliative surgical resection, radiation, and chemotherapy. Although no significant survival benefits have been shown by the surgical series, surgical resection may improve quality of life. Here we review the relevant literature and present six illustrative cases from our own institution. Hindawi Publishing Corporation 2012 2011-10-13 /pmc/articles/PMC3263702/ /pubmed/22312541 http://dx.doi.org/10.1155/2012/647256 Text en Copyright © 2012 Tamer Altay et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Altay, Tamer
Krisht, Khaled M.
Couldwell, William T.
Sellar and Parasellar Metastatic Tumors
title Sellar and Parasellar Metastatic Tumors
title_full Sellar and Parasellar Metastatic Tumors
title_fullStr Sellar and Parasellar Metastatic Tumors
title_full_unstemmed Sellar and Parasellar Metastatic Tumors
title_short Sellar and Parasellar Metastatic Tumors
title_sort sellar and parasellar metastatic tumors
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263702/
https://www.ncbi.nlm.nih.gov/pubmed/22312541
http://dx.doi.org/10.1155/2012/647256
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