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A 13-year patient journey of infant giant clival chordoma: case report and literature review
Chordomas are rare malignant bone tumours that develop from the ectopic remnants of the embryonic notochord. In contrast to adults, the majority in children under 16 present intra-cranially (63%). In 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159969/ https://www.ncbi.nlm.nih.gov/pubmed/36414866 http://dx.doi.org/10.1007/s00381-022-05749-4 |
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author | Apps, J. Gagen, R. Neumann, E. Solanki, G. English, M. |
author_facet | Apps, J. Gagen, R. Neumann, E. Solanki, G. English, M. |
author_sort | Apps, J. |
collection | PubMed |
description | Chordomas are rare malignant bone tumours that develop from the ectopic remnants of the embryonic notochord. In contrast to adults, the majority in children under 16 present intra-cranially (63%). In 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case to present without skull base involvement and the fourth case of chordoma in a patient with tuberous sclerosis (TS) Kombogiorgas (Childs Nerv Syst 22(10):1369–1374, 2006). In this report, we provide an update on this patient’s journey through a range of therapeutic options and summarize an update of the literature, since 2006, for this patient group. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00381-022-05749-4. |
format | Online Article Text |
id | pubmed-10159969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101599692023-05-06 A 13-year patient journey of infant giant clival chordoma: case report and literature review Apps, J. Gagen, R. Neumann, E. Solanki, G. English, M. Childs Nerv Syst Case Report Chordomas are rare malignant bone tumours that develop from the ectopic remnants of the embryonic notochord. In contrast to adults, the majority in children under 16 present intra-cranially (63%). In 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case to present without skull base involvement and the fourth case of chordoma in a patient with tuberous sclerosis (TS) Kombogiorgas (Childs Nerv Syst 22(10):1369–1374, 2006). In this report, we provide an update on this patient’s journey through a range of therapeutic options and summarize an update of the literature, since 2006, for this patient group. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00381-022-05749-4. Springer Berlin Heidelberg 2022-11-22 2023 /pmc/articles/PMC10159969/ /pubmed/36414866 http://dx.doi.org/10.1007/s00381-022-05749-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Apps, J. Gagen, R. Neumann, E. Solanki, G. English, M. A 13-year patient journey of infant giant clival chordoma: case report and literature review |
title | A 13-year patient journey of infant giant clival chordoma: case report and literature review |
title_full | A 13-year patient journey of infant giant clival chordoma: case report and literature review |
title_fullStr | A 13-year patient journey of infant giant clival chordoma: case report and literature review |
title_full_unstemmed | A 13-year patient journey of infant giant clival chordoma: case report and literature review |
title_short | A 13-year patient journey of infant giant clival chordoma: case report and literature review |
title_sort | 13-year patient journey of infant giant clival chordoma: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159969/ https://www.ncbi.nlm.nih.gov/pubmed/36414866 http://dx.doi.org/10.1007/s00381-022-05749-4 |
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