Autor: |
Alqarni, Naif, Alanazi, Awatif, Afaddagh, Abdulmohsin, Eldahshan, Samir, Alshayie, Mohammed, Alshammari, Ahmad |
Předmět: |
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Zdroj: |
Urology Annals; Jul-Sep2021, Vol. 13 Issue 3, p320-322, 3p |
Abstrakt: |
Renal cell carcinoma (RCC) in children is relatively uncommon, especially in the absence of syndromes or hereditary diseases. Duplex kidney – as a common congenital anomalies in children – is usually insignificant with no serious impact or known risk of tumor association. Herein, we report a 5-year-old girl who presented with gross hematuria and a right renal mass in duplex system identified on computed tomography. Radical nephrectomy was performed; the patient was diagnosed with Xp11 translocation RCC and no other modalities of treatments were needed over 3-month follow-up. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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