Larynx myofibroblastic tumor, a rare case report

Myofibroblastic tumors are extremely rare in the larynx, with just over 40 published cases. Despite being a benign tumor, it presents with a marked inflammatory character, local destruction, and the possibility of degeneration to malignant histological types with metastatic capacity. Anatomopatholog...

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Detalles Bibliográficos
Autores principales: Bazan Inostroza, Borja, Prada Pendolero, Jorge, Eisenberg Plaza, Gustavo, Adrados, Magdalena, Raboso García‐Baquero, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397474/
https://www.ncbi.nlm.nih.gov/pubmed/37546157
http://dx.doi.org/10.1002/ccr3.6281
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author Bazan Inostroza, Borja
Prada Pendolero, Jorge
Eisenberg Plaza, Gustavo
Adrados, Magdalena
Raboso García‐Baquero, Eduardo
author_facet Bazan Inostroza, Borja
Prada Pendolero, Jorge
Eisenberg Plaza, Gustavo
Adrados, Magdalena
Raboso García‐Baquero, Eduardo
author_sort Bazan Inostroza, Borja
collection PubMed
description Myofibroblastic tumors are extremely rare in the larynx, with just over 40 published cases. Despite being a benign tumor, it presents with a marked inflammatory character, local destruction, and the possibility of degeneration to malignant histological types with metastatic capacity. Anatomopathological differential diagnosis is fundamental in these cases.
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spelling pubmed-103974742023-08-04 Larynx myofibroblastic tumor, a rare case report Bazan Inostroza, Borja Prada Pendolero, Jorge Eisenberg Plaza, Gustavo Adrados, Magdalena Raboso García‐Baquero, Eduardo Clin Case Rep Case Report Myofibroblastic tumors are extremely rare in the larynx, with just over 40 published cases. Despite being a benign tumor, it presents with a marked inflammatory character, local destruction, and the possibility of degeneration to malignant histological types with metastatic capacity. Anatomopathological differential diagnosis is fundamental in these cases. John Wiley and Sons Inc. 2023-08-02 /pmc/articles/PMC10397474/ /pubmed/37546157 http://dx.doi.org/10.1002/ccr3.6281 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. 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 Report
Bazan Inostroza, Borja
Prada Pendolero, Jorge
Eisenberg Plaza, Gustavo
Adrados, Magdalena
Raboso García‐Baquero, Eduardo
Larynx myofibroblastic tumor, a rare case report
title Larynx myofibroblastic tumor, a rare case report
title_full Larynx myofibroblastic tumor, a rare case report
title_fullStr Larynx myofibroblastic tumor, a rare case report
title_full_unstemmed Larynx myofibroblastic tumor, a rare case report
title_short Larynx myofibroblastic tumor, a rare case report
title_sort larynx myofibroblastic tumor, a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397474/
https://www.ncbi.nlm.nih.gov/pubmed/37546157
http://dx.doi.org/10.1002/ccr3.6281
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