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The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report
Sclerosing epithelioid fibrosarcoma is an ultra-rare and aggressive high-grade fibrosarcoma that was originally described in 1995. More than 100 cases are documented worldwide, with the most extensive case series reporting a high rate of recurrence and metastasis. ALK mutations are commonly seen in...
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/PMC10601707/ https://www.ncbi.nlm.nih.gov/pubmed/37900840 http://dx.doi.org/10.1159/000532099 |
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author | Badran, Ahmed Steele, Clara Alquaydheb, Hisham Ba Theeb, Ahmed Bawazir, Abdulmalik Elshenawy, Mahmoud A. Atallah, Jean Paul |
author_facet | Badran, Ahmed Steele, Clara Alquaydheb, Hisham Ba Theeb, Ahmed Bawazir, Abdulmalik Elshenawy, Mahmoud A. Atallah, Jean Paul |
author_sort | Badran, Ahmed |
collection | PubMed |
description | Sclerosing epithelioid fibrosarcoma is an ultra-rare and aggressive high-grade fibrosarcoma that was originally described in 1995. More than 100 cases are documented worldwide, with the most extensive case series reporting a high rate of recurrence and metastasis. ALK mutations are commonly seen in soft-tissue sarcomas; however, this is the first known case of an ALK V757M mutation. Here, we present a case using crizotinib in treating an ALK-positive sclerosing epithelioid fibrosarcoma refractory to all traditional treatment options. |
format | Online Article Text |
id | pubmed-10601707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106017072023-10-27 The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report Badran, Ahmed Steele, Clara Alquaydheb, Hisham Ba Theeb, Ahmed Bawazir, Abdulmalik Elshenawy, Mahmoud A. Atallah, Jean Paul Case Rep Oncol Case Report Sclerosing epithelioid fibrosarcoma is an ultra-rare and aggressive high-grade fibrosarcoma that was originally described in 1995. More than 100 cases are documented worldwide, with the most extensive case series reporting a high rate of recurrence and metastasis. ALK mutations are commonly seen in soft-tissue sarcomas; however, this is the first known case of an ALK V757M mutation. Here, we present a case using crizotinib in treating an ALK-positive sclerosing epithelioid fibrosarcoma refractory to all traditional treatment options. S. Karger AG 2023-08-28 /pmc/articles/PMC10601707/ /pubmed/37900840 http://dx.doi.org/10.1159/000532099 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 Badran, Ahmed Steele, Clara Alquaydheb, Hisham Ba Theeb, Ahmed Bawazir, Abdulmalik Elshenawy, Mahmoud A. Atallah, Jean Paul The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report |
title | The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report |
title_full | The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report |
title_fullStr | The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report |
title_full_unstemmed | The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report |
title_short | The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report |
title_sort | use of crizotinib in sclerosing epithelioid fibrosarcoma with alk mutation: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601707/ https://www.ncbi.nlm.nih.gov/pubmed/37900840 http://dx.doi.org/10.1159/000532099 |
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