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Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles
The risk stratification of infants with metastatic neuroblastoma (NB) has evolved over time from stage 4/M or IVs/4S/MS/Ms according to various staging systems. Despite these developments for some genetic aberrations, the prognostic value and the impact of soft tissue metastases in infants are not f...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601722/ https://www.ncbi.nlm.nih.gov/pubmed/37900821 http://dx.doi.org/10.1159/000531433 |
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author | van Heerden, Jaques van den Akker, Machiel Verlooy, Joris Van Roy, Nadine Laureys, Geneviève Norga, Koen |
author_facet | van Heerden, Jaques van den Akker, Machiel Verlooy, Joris Van Roy, Nadine Laureys, Geneviève Norga, Koen |
author_sort | van Heerden, Jaques |
collection | PubMed |
description | The risk stratification of infants with metastatic neuroblastoma (NB) has evolved over time from stage 4/M or IVs/4S/MS/Ms according to various staging systems. Despite these developments for some genetic aberrations, the prognostic value and the impact of soft tissue metastases in infants are not fully understood, nor well described in the different classification systems, hampering the definitions to uniformly treat patients and predict prognosis. A literature review on staging of infants with M/MS disease was performed at the occasion of the diagnosis of NB in an 8-month-old boy who presented with atypical metastatic sites in soft tissue and an aberrant tumor biology. The definitions of stage 4/4S/4s/M/MS/Ms were evaluated and compared to enable tumor risk stratification and inform management. International NB groups use different criteria for defining stage of infants with metastasized NB, resulting in differences in management. Limited literature is available on soft tissue metastases, especially muscular metastases, and is poorly incorporated into management guidelines mainly due to the lack of data. The uncertain prognosis of rare genetic aberrancies may add to the difficulties in treatment decisions. In some rare cases of NB in infants, the international treatment classification is not sufficient for staging and treatment decisions. Based on tumor progression, biology of unknown significance and a lack of evidence to classify a child under 12 months with NB and multiple muscular metastases, the patient was treated as stage 4/M and intermediate-risk protocols with a favorable outcome. |
format | Online Article Text |
id | pubmed-10601722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106017222023-10-27 Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles van Heerden, Jaques van den Akker, Machiel Verlooy, Joris Van Roy, Nadine Laureys, Geneviève Norga, Koen Case Rep Oncol Case Report The risk stratification of infants with metastatic neuroblastoma (NB) has evolved over time from stage 4/M or IVs/4S/MS/Ms according to various staging systems. Despite these developments for some genetic aberrations, the prognostic value and the impact of soft tissue metastases in infants are not fully understood, nor well described in the different classification systems, hampering the definitions to uniformly treat patients and predict prognosis. A literature review on staging of infants with M/MS disease was performed at the occasion of the diagnosis of NB in an 8-month-old boy who presented with atypical metastatic sites in soft tissue and an aberrant tumor biology. The definitions of stage 4/4S/4s/M/MS/Ms were evaluated and compared to enable tumor risk stratification and inform management. International NB groups use different criteria for defining stage of infants with metastasized NB, resulting in differences in management. Limited literature is available on soft tissue metastases, especially muscular metastases, and is poorly incorporated into management guidelines mainly due to the lack of data. The uncertain prognosis of rare genetic aberrancies may add to the difficulties in treatment decisions. In some rare cases of NB in infants, the international treatment classification is not sufficient for staging and treatment decisions. Based on tumor progression, biology of unknown significance and a lack of evidence to classify a child under 12 months with NB and multiple muscular metastases, the patient was treated as stage 4/M and intermediate-risk protocols with a favorable outcome. S. Karger AG 2023-07-26 /pmc/articles/PMC10601722/ /pubmed/37900821 http://dx.doi.org/10.1159/000531433 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission |
spellingShingle | Case Report van Heerden, Jaques van den Akker, Machiel Verlooy, Joris Van Roy, Nadine Laureys, Geneviève Norga, Koen Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles |
title | Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles |
title_full | Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles |
title_fullStr | Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles |
title_full_unstemmed | Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles |
title_short | Dilemmas in the Management of an Infant with Neuroblastoma Metastasized to the Muscles |
title_sort | dilemmas in the management of an infant with neuroblastoma metastasized to the muscles |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601722/ https://www.ncbi.nlm.nih.gov/pubmed/37900821 http://dx.doi.org/10.1159/000531433 |
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