2018
DOI: 10.1159/000486640
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Concomitant Non-Small Cell Lung Cancer and Hairy Cell Leukemia in a Patient Harboring BRAF-V600E Mutation in Both Tissues: A Case Report

Abstract: The BRAF-V600E mutation has been established as a signature alteration occurring almost universally in hairy cell leukemia. Moreover, it can be detected in a small percentage of patients with non-small cell lung cancer. We report the case of a patient with a metastatic BRAF-V600E-mutated lung adenocarcinoma suffering from concomitant hairy cell leukemia. The identification of an identical BRAF mutation in both malignancies raises physiopathological considerations and might offer unique therapeutic strategies f… Show more

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Cited by 5 publications
(2 citation statements)
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“…The BRAF gene is mutated in 1–5% of NSCLC cases and most of these mutations occur in adenocarcinoma (14). BRAF is a member of the RAF family of serine/threonine kinases that mediate signal transduction between RAS and mitogen-activated protein kinase (MAPK) signaling pathways (15). Once the mutation is activated, the downstream mitogen-actiavted protein kinase (MEK)-extracellular regulated protein kinase signaling pathway is activated continuously, resulting in the excessive proliferation and survival of tumor cells (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The BRAF gene is mutated in 1–5% of NSCLC cases and most of these mutations occur in adenocarcinoma (14). BRAF is a member of the RAF family of serine/threonine kinases that mediate signal transduction between RAS and mitogen-activated protein kinase (MAPK) signaling pathways (15). Once the mutation is activated, the downstream mitogen-actiavted protein kinase (MEK)-extracellular regulated protein kinase signaling pathway is activated continuously, resulting in the excessive proliferation and survival of tumor cells (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The reported cancers include hairy cell leukemia, melanoma, and adenocarcinoma of the lung. [22][23][24][25] In conclusion, we report a novel poly-neoplastic syndrome associated with BRAF p.V600E mutation. As next generation sequencing is becoming more available in cancer diagnosis, more cases with this syndrome may be discovered.…”
Section: Discussionmentioning
confidence: 62%