“…Relative to its genetic origin, as commented before, mutations in the BRAF oncogene are found in approximately 50% of MM, but they are also observed in other cancers such as hairy cell leukemia, papillary thyroid cancers, colorectal cancer, liver cancer, brain cancer, lung cancer, soft tissue cancer, ovarian cancer, and breast cancer, with varying rates ranging from 2% to 100% [28]. However, there is no established association between BRAF positivity in previous MM and the development of SPNs, possibly due to the somatic nature of the mutation rather than being inherited or germline [28]. On the other hand, germline mutations in BRCA2 or CDKN2A have been suggested as explanations for the link between MM and breast cancer, and CDKN2A mutations have also been proposed as a cause of the increased risk of pancreatic cancer.…”