NSCLC With Synchronous EGFR Mutations in Li Fraumeni Syndrome: A Case Report

We report a case of a patient with Li Fraumeni Syndrome (LFS) who developed synchronous EGFR exon deletion 19 and EGFR exon 20 insertion NSCLC and characterize the diagnostic and therapeutic challenges in managing her care. Osimertinib was effective in the EGFR deletion 19 population but did not gar...

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Detalles Bibliográficos
Autores principales: Marks, Jennifer A., Liu, Stephen V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209531/
https://www.ncbi.nlm.nih.gov/pubmed/37251503
http://dx.doi.org/10.1016/j.jtocrr.2023.100521

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209531/
https://www.ncbi.nlm.nih.gov/pubmed/37251503
http://dx.doi.org/10.1016/j.jtocrr.2023.100521

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