Renal cell carcinoma in a duplex kidney in pediatric

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-...

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Detalles Bibliográficos
Autores principales: Alqarni, Naif, Alanazi, Awatif, Afaddagh, Abdulmohsin, Eldahshan, Samir, Alshayie, Mohammed, Alshammari, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343276/
https://www.ncbi.nlm.nih.gov/pubmed/34421274
http://dx.doi.org/10.4103/UA.UA_126_20
Descripción
Sumario: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.

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