Familial Syndromes Coupling with Small Renal Masses
Author Information
Author(s): Jorge Hidalgo, Gilberto Chéchile
Primary Institution: Instituto Medico Tecnológico, Barcelona, Spain
Hypothesis
The aim of our work is to review the features of hereditary renal cancers and the various histopathologic features of renal cancer.
Conclusion
Hereditary renal cancers can lead to multiple and/or bilateral kidney tumors, and nephron-sparing surgery can preserve renal function while maintaining oncology efficacy for selected patients.
Supporting Evidence
- Hereditary renal cancer syndromes can lead to multiple bilateral kidney tumors that occur at a younger age than nonhereditary renal cancers.
- Nephron-sparing surgery has the potential to preserve renal function while maintaining oncology efficacy for appropriately selected patients.
- The 3 cm threshold is a point at which the risk of metastasis is balanced with the potential morbidities of multiple procedures.
Takeaway
Some families have a higher chance of getting kidney cancer because of their genes, and doctors need to be careful when treating these patients.
Methodology
The study involved reviewing hereditary renal cancer features and analyzing families with multiple members affected by renal carcinoma.
Limitations
The study does not provide specific data on the effectiveness of different treatment strategies for each syndrome.
Participant Demographics
The study included families with multiple members affected by renal carcinoma, specifically focusing on hereditary syndromes.
Digital Object Identifier (DOI)
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