Pediatric soft tissue neoplasms with BRAF activating mutations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pathology and Forensic Medicine
Link
http://www.nature.com/articles/s41379-021-00852-4.pdf
Reference12 articles.
1. Penning AJ, Al-Ibraheemi A, Michal M, Larsen BT, Cho S-J, Lockwood CM, et al. Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma. Mod Pathol. 2021. https://doi.org/10.1038/s41379-021-00806-w.
2. Smith SC, Mochel M, Wojcik J, Gowda M, Patel R. A novel, low-grade paediatric soft tissue neoplasm defined by BRAF mutation. Virchows Arch. 2018;473:S23.
3. Suurmeijer AJH, Dickson BC, Swanson D, Zhang L, Sung YS, Cotzia P, et al. A novel group of spindle cell tumors defined by S100 and CD34 co-expression shows recurrent fusions involving RAF1, BRAF, and NTRK1/2 genes. Genes Chromosomes Cancer. 2018;57:611–21.
4. Kao YC, Fletcher CDM, Alaggio R, Wexler L, Zhang L, Sung YS, et al. Recurrent BRAF gene fusions in a subset of pediatric spindle cell sarcomas: expanding the genetic spectrum of tumors with overlapping features with infantile fibrosarcoma. Am J Surg Pathol. 2018;42:28–38.
5. Miyamoto M, Tsunoda R, Gembun Y, Konno S, Hagiwara Y, Liu X, et al. Recurrence of fibrous hamartoma of infancy excised 14 years after the primary surgery. J Neurosurg Pediatr. 2010;5:136–9.
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