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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...

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Detalles Bibliográficos
Autores principales: Clarke, Jamie E., Magoon, Stephanie, Forghani, Irman, Alessandrino, Francesco, D’Amato, Gina, Jonczak, Emily, Subhawong, Ty K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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