Carcinoma de células renais claras e de origem genética: relato de caso

Abstract

The purpose of this research was to characterize the management and treatment of a pathology, specifically a rare case of bilateral renal neoplasia, with reference to the information obtained from the patient's medical record and outpatient follow-up. The research method used was the case report, in which the methodology adopted was based on the chronological collection of data from medical records, from hospital admission to outpatient follow-ups. The patient in question was a 33-year-old male, being followed from his diagnosis to his current treatment phase. He was admitted to the Emergency Department of the Maria Aparecida Pedrossian University Hospital with macroscopic hematuria associated with bilateral flank pain. Contrast tomography was performed, showing evidence of polycystic renal and pancreatic disease, in addition to bilateral neoplastic lesions. A right partial nephrectomy was also performed and a genetic research was carried out with a diagnosis of von Hippel-Lindau disease, which should be remembered in patients with renal neoplasia, especially associated with other commemorative, and its diagnosis allows the patient a more assertive and individualized clinical management.