Karl J. D'Silva, MD, reviews the recommendations for early diagnosis and management of hereditary RCC.
Clinical Assistant Professor of Medicine, Department of Hematology and Oncology, Tufts University School of Medicine; Medical Director, Lahey Hospitals and Medical Center, Burlington, Massachusetts are associated with genetic syndromes that may affect multiple family members across generations. Karl J.
The finding of a VHL pathogenic variant is considered a genetic diagnosis and should prompt clinical surveillance and treatment. Some individuals meet the clinical criteria for VHL diagnosis but do not have family history of VHL. In these instances, a de novo pathogenic variant or mosaicism should be considered.Yes, genetic testing can significantly affect patient management in VHL.
Renal Cell Cancer RCC - Renal Cell Carcinoma Cancer Of The Kidney Renal Cell Carcinoma RCC Genomics Genomic Medicine Genetics Genetic Testing Neuroendocrine Tumor Neuroendocrine Tumour NET Nets Neuroendocrine Tumor (NET) Neuroendocrine Tumors (Nets) Neuroendocrine Tumour (NET) Neuroendocrine Tumours (Nets) Tumor Cancer Malignant Neoplasia Carcinoma
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