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Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer

Hereditary medullary thyroid cancer is an aggressive cancer for which there is no standard effective systemic therapy, but which can be prevented through genetic screening and prophylactic thyroidectomy. Although this cancer accounts for roughly 17% of all pediatric thyroid cancers, a significant pe...

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Autores principales: Rosenthal, MSara, Diekema, DouglasS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198744/
https://www.ncbi.nlm.nih.gov/pubmed/21436957
http://dx.doi.org/10.1155/2011/847603
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author Rosenthal, MSara
Diekema, DouglasS
author_facet Rosenthal, MSara
Diekema, DouglasS
author_sort Rosenthal, MSara
collection PubMed
description Hereditary medullary thyroid cancer is an aggressive cancer for which there is no standard effective systemic therapy, but which can be prevented through genetic screening and prophylactic thyroidectomy. Although this cancer accounts for roughly 17% of all pediatric thyroid cancers, a significant percentage of affected families do not "accept" screening, while many gene carriers delay or refuse prophylactic thyroid surgery for their children. Current genetic screening practices in medullary thyroid cancer are inadequate; more than 50% of index patients with hereditary medullary thyroid cancer present with a thyroid mass; up to 75% have distant metastasis. These proposed pediatric ethics guidelines focus on two ethical issues that affect at-risk children: (1) how do we identify at-risk children whose RET-positive relative refuses to disclose that they carry the mutation? (2) How do we protect RET-positive children whose parents refuse prophylactic thyroidectomy?
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spelling pubmed-31987442011-10-23 Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer Rosenthal, MSara Diekema, DouglasS Int J Pediatr Endocrinol Commentary Hereditary medullary thyroid cancer is an aggressive cancer for which there is no standard effective systemic therapy, but which can be prevented through genetic screening and prophylactic thyroidectomy. Although this cancer accounts for roughly 17% of all pediatric thyroid cancers, a significant percentage of affected families do not "accept" screening, while many gene carriers delay or refuse prophylactic thyroid surgery for their children. Current genetic screening practices in medullary thyroid cancer are inadequate; more than 50% of index patients with hereditary medullary thyroid cancer present with a thyroid mass; up to 75% have distant metastasis. These proposed pediatric ethics guidelines focus on two ethical issues that affect at-risk children: (1) how do we identify at-risk children whose RET-positive relative refuses to disclose that they carry the mutation? (2) How do we protect RET-positive children whose parents refuse prophylactic thyroidectomy? BioMed Central 2011 2011-02-06 /pmc/articles/PMC3198744/ /pubmed/21436957 http://dx.doi.org/10.1155/2011/847603 Text en Copyright © 2011 Copyright © 2011 M. Sara Rosenthal and Douglas S. Diekema. https://creativecommons.org/licenses/by/4.0/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 Commentary
Rosenthal, MSara
Diekema, DouglasS
Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer
title Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer
title_full Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer
title_fullStr Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer
title_full_unstemmed Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer
title_short Pediatric Ethics Guidelines for Hereditary Medullary Thyroid Cancer
title_sort pediatric ethics guidelines for hereditary medullary thyroid cancer
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198744/
https://www.ncbi.nlm.nih.gov/pubmed/21436957
http://dx.doi.org/10.1155/2011/847603
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