A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review

The plexiform fibrohistiocytic tumor (PFHT) is an infrequent soft-tissue neoplasm with uncertain biological behavior. We report a rare congenital PFHT case in a 4-year-old boy, treated with wide excision and skin grafting. After a 52-month follow-up, no recurrence, regional or distant metastases wer...

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Autores principales: Demiri, Efterpi, Georgiadou, Eleni, Goula, Olga-Christina, Tzorakoeleftheraki, Sofia-Eleni, Karagergou, Eleni, Hytiroglou, Prodromos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491708/
https://www.ncbi.nlm.nih.gov/pubmed/34621916
http://dx.doi.org/10.1080/23320885.2021.1986049
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author Demiri, Efterpi
Georgiadou, Eleni
Goula, Olga-Christina
Tzorakoeleftheraki, Sofia-Eleni
Karagergou, Eleni
Hytiroglou, Prodromos
author_facet Demiri, Efterpi
Georgiadou, Eleni
Goula, Olga-Christina
Tzorakoeleftheraki, Sofia-Eleni
Karagergou, Eleni
Hytiroglou, Prodromos
author_sort Demiri, Efterpi
collection PubMed
description The plexiform fibrohistiocytic tumor (PFHT) is an infrequent soft-tissue neoplasm with uncertain biological behavior. We report a rare congenital PFHT case in a 4-year-old boy, treated with wide excision and skin grafting. After a 52-month follow-up, no recurrence, regional or distant metastases were documented. A literature review on the management of PFHTs is reported.
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spelling pubmed-84917082021-10-06 A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review Demiri, Efterpi Georgiadou, Eleni Goula, Olga-Christina Tzorakoeleftheraki, Sofia-Eleni Karagergou, Eleni Hytiroglou, Prodromos Case Reports Plast Surg Hand Surg Case Report The plexiform fibrohistiocytic tumor (PFHT) is an infrequent soft-tissue neoplasm with uncertain biological behavior. We report a rare congenital PFHT case in a 4-year-old boy, treated with wide excision and skin grafting. After a 52-month follow-up, no recurrence, regional or distant metastases were documented. A literature review on the management of PFHTs is reported. Taylor & Francis 2021-10-01 /pmc/articles/PMC8491708/ /pubmed/34621916 http://dx.doi.org/10.1080/23320885.2021.1986049 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Demiri, Efterpi
Georgiadou, Eleni
Goula, Olga-Christina
Tzorakoeleftheraki, Sofia-Eleni
Karagergou, Eleni
Hytiroglou, Prodromos
A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
title A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
title_full A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
title_fullStr A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
title_full_unstemmed A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
title_short A rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
title_sort rare case of congenital plexiform fibrohistiocytic tumor of the foot in a 4-year-old boy: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491708/
https://www.ncbi.nlm.nih.gov/pubmed/34621916
http://dx.doi.org/10.1080/23320885.2021.1986049
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