A case report of infantile fibrosarcoma with BRAF gene mutation with incomplete intestinal obstruction
Intestinal IFS is a rare soft tissue sarcoma predominantly occurring in early infancy. Cases involving the BRAF p.V600delinsDL mutation are even rarer. Treatment should be individualized, with complete surgical resection being the cornerstone of therapy. Prognosis remains favorable following complete excision.
Authors
- Gaofeng Cui (ORCID: https://orcid.org/0000-0002-7900-173X)
- Jian Hai (ORCID: https://orcid.org/0000-0002-1609-5556)
- Hongjie Zhou (ORCID: https://orcid.org/0000-0002-7156-188X)
- Fan Liang (ORCID: https://orcid.org/0009-0000-1531-0974)
- Fan Chen (ORCID: https://orcid.org/0000-0002-5739-2776)
- Fan Zhu (ORCID: https://orcid.org/0000-0003-3817-4674)
- Jianfeng Xu (ORCID: https://orcid.org/0000-0003-4776-2910)
Institutions
- Huizhou Central People's Hospital (CN)
- Huizhou University (CN)
Publication Details
- Journal
- Frontiers in Oncology
- Published
- 2025-01-29
- DOI
- https://doi.org/10.3389/fonc.2025.1492654
- Primary Topic
- Sarcoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00