Autor: |
Leitão, Victor Augusto, Da Silva Jr., Walter, Ferreira, Ubirajara, Denardi, Fernandes, Billis, Athanase, Netto Jr., Nelson Rodrigues |
Předmět: |
|
Zdroj: |
Urologia Internationalis; Aug2006, Vol. 77 Issue 2, p184-186, 3p |
Abstrakt: |
Young patients with sickle cell trait or disease present a higher risk for renal medullary carcinoma, an aggressive renal tumor, with dismal prognosis, with a median survival of 4 months from the time of diagnosis. We report a 26-year-old patient with a 2-month history of bone pain at the right iliac crest, loss of weight, recurrent macroscopic hematuria and abdominal mass. Imaging studies demonstrated a 10-cm mass in the right kidney. Pathological evaluation revealed a medullary carcinoma and the patient died after 4 months, despite adjuvant treatment. Whenever a patient with sickle cell trait or disease presents with hematuria and/or flank pain, the possibility of a renal medullary carcinoma should always be kept in mind, with thorough investigation and expeditious treatment. Copyright © 2006 S. Karger AG, Basel [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
|