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Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature

BACKGROUND: Ewing's sarcoma rarely presents in bones of the feet. Surgical management usually includes amputation. Limb sparing surgery is anecdotal. CASE: We report the case of a 13‐year‐old boy with an Ewing sarcoma in his calcaneus who had a calcaneal reconstruction with total calcaneus allo...

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Autores principales: Torner, Ferran, Nuñez, Jorge H., Inarejos Clemente, Emilio José, Garraus, Moira, Suñol, Mariona, Martínez, Aníbal D., Moreno, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458496/
https://www.ncbi.nlm.nih.gov/pubmed/35583247
http://dx.doi.org/10.1002/cnr2.1626
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author Torner, Ferran
Nuñez, Jorge H.
Inarejos Clemente, Emilio José
Garraus, Moira
Suñol, Mariona
Martínez, Aníbal D.
Moreno, David
author_facet Torner, Ferran
Nuñez, Jorge H.
Inarejos Clemente, Emilio José
Garraus, Moira
Suñol, Mariona
Martínez, Aníbal D.
Moreno, David
author_sort Torner, Ferran
collection PubMed
description BACKGROUND: Ewing's sarcoma rarely presents in bones of the feet. Surgical management usually includes amputation. Limb sparing surgery is anecdotal. CASE: We report the case of a 13‐year‐old boy with an Ewing sarcoma in his calcaneus who had a calcaneal reconstruction with total calcaneus allograft after induction chemotherapy. CONCLUSIONS: At 42 months of follow‐up our patient remains disease free and functionally intact. A review of the exceptional limb salvage procedure options for malignant calcaneus tumor was performed.
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spelling pubmed-94584962022-09-12 Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature Torner, Ferran Nuñez, Jorge H. Inarejos Clemente, Emilio José Garraus, Moira Suñol, Mariona Martínez, Aníbal D. Moreno, David Cancer Rep (Hoboken) Case Reports BACKGROUND: Ewing's sarcoma rarely presents in bones of the feet. Surgical management usually includes amputation. Limb sparing surgery is anecdotal. CASE: We report the case of a 13‐year‐old boy with an Ewing sarcoma in his calcaneus who had a calcaneal reconstruction with total calcaneus allograft after induction chemotherapy. CONCLUSIONS: At 42 months of follow‐up our patient remains disease free and functionally intact. A review of the exceptional limb salvage procedure options for malignant calcaneus tumor was performed. John Wiley and Sons Inc. 2022-05-18 /pmc/articles/PMC9458496/ /pubmed/35583247 http://dx.doi.org/10.1002/cnr2.1626 Text en © 2022 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Torner, Ferran
Nuñez, Jorge H.
Inarejos Clemente, Emilio José
Garraus, Moira
Suñol, Mariona
Martínez, Aníbal D.
Moreno, David
Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature
title Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature
title_full Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature
title_fullStr Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature
title_full_unstemmed Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature
title_short Total calcaneal allograft reconstruction of an Ewing's sarcoma in a child: Outcome and review of the literature
title_sort total calcaneal allograft reconstruction of an ewing's sarcoma in a child: outcome and review of the literature
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458496/
https://www.ncbi.nlm.nih.gov/pubmed/35583247
http://dx.doi.org/10.1002/cnr2.1626
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