Case series of adult Wilms’ tumor and review of the literature
AWT is a relatively rare malignant tumor with a low preoperative diagnostic accuracy and a poorer prognosis than children. Early diagnosis, successful surgery, and standardized postoperative adjuvant therapy according to pathological typing and staging are the key points to improve the survival of AWT patients.
Authors
- Qi Gao (ORCID: https://orcid.org/0000-0002-1965-7411)
- Yang Luan (ORCID: https://orcid.org/0000-0001-7153-3814)
- Fan Yang (ORCID: https://orcid.org/0000-0001-6227-9113)
- Xiang Yu (ORCID: https://orcid.org/0000-0002-5269-3975)
- Ying He (ORCID: https://orcid.org/0000-0002-6491-0105)
- Zhong Chen (ORCID: https://orcid.org/0000-0003-3016-2281)
- Xiaoqin Chen (ORCID: https://orcid.org/0000-0003-0491-5753)
Institutions
- Tongji Hospital (CN)
- Huazhong University of Science and Technology (CN)
Publication Details
- Journal
- AME Case Reports
- Published
- 2025-04-01
- DOI
- https://doi.org/10.21037/acr-24-208
- Primary Topic
- Renal and related cancers
- Type
- article
- Field-Weighted Citation Impact
- 0.00