The "Wilms tumor; Case report". "Nephroblastoma; Case report".

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Kassandra Aglae Salazar Vázquez
Yanyn Ameyaly Cabrera Antonio
Arturo Gerardo Garza Alatorre
Verónica Rodríguez Martínez
Rosario del Carmen Medellín Vallejo
Marco Antonio Ponce Camacho

Abstract

Background: Nephroblastoma, also known as Wilms tumor, is the second most common intra-abdominal tumor and the most prevalent renal tumor in the pediatric age group, predominantly occurring between 1 and 5 years of age, with bilateral presentation being rare.


Case Report: In this case study, we describe a typical symptom presentation, albeit with the unique aspect of bilateral tumor involvement—a rarity. We delve into the patient's management and observe a favorable progression in their condition.


Conclusion: The significance of this study lies in its assertion as one of the pediatric tumors with an excellent prognosis when detected at an early stage. Conversely, prognosis tends to be slightly worse in advanced stages, emphasizing the critical role of timely diagnosis within pediatric clinical practice.

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How to Cite
Salazar Vázquez, K. A., Cabrera Antonio, Y. A., Garza Alatorre, A. G., Rodríguez Martínez, V., Medellín Vallejo, R. del C., & Ponce Camacho, M. A. (2023). The "Wilms tumor; Case report".: "Nephroblastoma; Case report". Pediatría, 56(3), e421. https://doi.org/10.14295/rp.v56i3.421
Section
Case report

References

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- Laura Illade, Carmen Hernandez-Marques, Maria Cormezana, Álvaro Lassaletta, Maitane Andión Catalán, David Ruano, Victoria Fioravantii y Luis Madero López. Tumor de Wilms: revisión de nuestra experiencia en los últimos 15 años. An Pediatr. 2018 (88) 140 – 149. DOI: https://doi.org/10.1016/j.anpedi.2017.03.019

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