The diagnosis, genetic alternation, and treatment of the primary pleomorphic liposarcoma of the femur in a rare age: Case report and literature review
Primary pleomorphic liposarcoma can present as sclerotic and aggressive malignant bone tumors at an early age. Excision, MAP, and MAPI chemotherapy are not enough to treat this tumor.
Authors
- Kirellos Said Abbas (ORCID: https://orcid.org/0000-0003-0339-9339)
- Hangchi Wang
- Basel Abdelazeem (ORCID: https://orcid.org/0000-0002-2919-6196)
- Hassan Abdalshafy
- Haixiao Wu (ORCID: https://orcid.org/0000-0002-2699-466X)
- Chao Zhang (ORCID: https://orcid.org/0000-0001-7096-8488)
- Ahmed K Ghanem
- Jin Zhang (ORCID: https://orcid.org/0000-0003-3554-2996)
Institutions
- Cairo University (EG)
- McLaren Health Care (US)
- UCLA Medical Center (US)
- Tianjin Medical University Cancer Institute and Hospital (CN)
- Tianjin Medical University (CN)
- Alexandria University (EG)
- Michigan State University (US)
Publication Details
- Journal
- Heliyon
- Published
- 2024-08-29
- DOI
- https://doi.org/10.1016/j.heliyon.2024.e36953
- Primary Topic
- Sarcoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Army Medical University