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Radiologic screening and surveillance in hereditary cancers
Hereditary cancer syndromes comprise an important subset of cancers caused by pathogenic germline mutations that can affect various organ systems. Radiologic screening and surveillance for solid tumors has emerged as a critical component of patient management in permitting early cancer detection. Al...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301608/ https://www.ncbi.nlm.nih.gov/pubmed/35874798 http://dx.doi.org/10.1016/j.ejro.2022.100422 |
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author | Clarke, Jamie E. Magoon, Stephanie Forghani, Irman Alessandrino, Francesco D’Amato, Gina Jonczak, Emily Subhawong, Ty K. |
author_facet | Clarke, Jamie E. Magoon, Stephanie Forghani, Irman Alessandrino, Francesco D’Amato, Gina Jonczak, Emily Subhawong, Ty K. |
author_sort | Clarke, Jamie E. |
collection | PubMed |
description | Hereditary cancer syndromes comprise an important subset of cancers caused by pathogenic germline mutations that can affect various organ systems. Radiologic screening and surveillance for solid tumors has emerged as a critical component of patient management in permitting early cancer detection. Although imaging surveillance may be tailored for organ-specific cancer risks, surveillance protocols frequently utilize whole-body MRI or PET/CT because of their ability to identify neoplasms in different anatomic regions in a single exam. In this review, we discuss the basic tenets of imaging screening and surveillance strategies in these syndromes, highlighting the more common neoplasms and their associated multimodality imaging findings. |
format | Online Article Text |
id | pubmed-9301608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-93016082022-07-22 Radiologic screening and surveillance in hereditary cancers Clarke, Jamie E. Magoon, Stephanie Forghani, Irman Alessandrino, Francesco D’Amato, Gina Jonczak, Emily Subhawong, Ty K. Eur J Radiol Open Article Hereditary cancer syndromes comprise an important subset of cancers caused by pathogenic germline mutations that can affect various organ systems. Radiologic screening and surveillance for solid tumors has emerged as a critical component of patient management in permitting early cancer detection. Although imaging surveillance may be tailored for organ-specific cancer risks, surveillance protocols frequently utilize whole-body MRI or PET/CT because of their ability to identify neoplasms in different anatomic regions in a single exam. In this review, we discuss the basic tenets of imaging screening and surveillance strategies in these syndromes, highlighting the more common neoplasms and their associated multimodality imaging findings. Elsevier 2022-04-25 /pmc/articles/PMC9301608/ /pubmed/35874798 http://dx.doi.org/10.1016/j.ejro.2022.100422 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Clarke, Jamie E. Magoon, Stephanie Forghani, Irman Alessandrino, Francesco D’Amato, Gina Jonczak, Emily Subhawong, Ty K. Radiologic screening and surveillance in hereditary cancers |
title | Radiologic screening and surveillance in hereditary cancers |
title_full | Radiologic screening and surveillance in hereditary cancers |
title_fullStr | Radiologic screening and surveillance in hereditary cancers |
title_full_unstemmed | Radiologic screening and surveillance in hereditary cancers |
title_short | Radiologic screening and surveillance in hereditary cancers |
title_sort | radiologic screening and surveillance in hereditary cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301608/ https://www.ncbi.nlm.nih.gov/pubmed/35874798 http://dx.doi.org/10.1016/j.ejro.2022.100422 |
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