An extremely rare case of concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma: case report and review of literature

BRAF protein is a serine/threonine kinase with 766 amino acids. Approximately 15% of human cancers harbor BRAF mutations as well as other BRAF anomalies (amplifications, fusions). Somatic mutations mainly occur in the catalytic kinase domain (CR3), and the predominant mutation is p.V600E which is th...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Autops Case Rep
Päätekijät: Ghorbani-Aghbolaghi, Amir, Lechpammer, Mirna, Ali, Saba F., Ku, Nam K., Dwyre, Denis M., Rashidi, Hooman H.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2017
Aiheet:
Article / Clinical Case Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5634429/
https://ncbi.nlm.nih.gov/pubmed/29043205
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4322/acr.2017.032
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