Unclassifiable renal carcinoma with medullary phenotype and SMARCB1 deficiency: case report
Given the rarity of unclassified RCC with a medullary phenotype, continuous documentation and analysis of individual cases not associated with sickle cell trait are crucial to understanding its behavior, prognosis, and potential therapeutic approaches, considering its aggressiveness and high metastatic potential.
Authors
- A Cavalli
- Samya Hamad Mehanna (ORCID: https://orcid.org/0000-0002-6636-1314)
- Thiago Hota (ORCID: https://orcid.org/0000-0003-4544-0539)
- Fernando C. Koleski
- Cacá Machado (ORCID: https://orcid.org/0000-0001-5175-8346)
- Linda Wolff
- Thiago Gabriel Ronkoski
Institutions
- Hospital Nossa Senhora das Graças (BR)
- Faculdade Evangélica do Paraná (BR)
Publication Details
- Journal
- Frontiers in Urology
- Published
- 2025-06-06
- DOI
- https://doi.org/10.3389/fruro.2025.1582675
- Citations
- 2
- Primary Topic
- Chromatin Remodeling and Cancer
- Type
- article
- Field-Weighted Citation Impact
- 1.61