Baby No More: A Rare Case of Papillary Renal Cell Carcinoma in a One Year Old Female

Donnel Guenter Rubio; Carlos Ramon Torres Jr.

Vol. 28 No. 2 (2018), Case Report

Vol. 28 No. 2 (2018)

Baby No More: A Rare Case of Papillary Renal Cell Carcinoma in a One Year Old Female

Case Report

Published 2020-03-05

Donnel Guenter Rubio, MD⁺⁻
Carlos Ramon N. Torres Jr., MD, FPUA⁺⁻

Donnel Guenter Rubio, MD

Department of Urology, National Kidney and Transplant Institute

Carlos Ramon N. Torres Jr., MD, FPUA

Department of Urology, National Kidney and Transplant Institute

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Keywords

Renal cell carcinoma
RCC
transabdominal radical nephrectomy
papillary renal cell carcinoma type 1
Vimentin

How to Cite

Rubio, D. G., & Torres Jr., C. R. (2020). Baby No More: A Rare Case of Papillary Renal Cell Carcinoma in a One Year Old Female. Philippine Journal of Urology, 28(2), 122–125. Retrieved from https://pjuonline.com/index.php/pju/article/view/78

Abstract

Renal cell carcinoma is the most common renal malignancy in adults and extremely rare in children. It may present with hematuria, flank pain and palpable mass. Treatment protocols for renal cell carcinoma in children have not yet been well-defined due to the rarity of the desease, however surgery remains the mainstay treatment for tumors that are resectable. Presented here is a case of a 1 year old female presenting with left hemiabdominal mass, who underwent transabdominal left radical nephrectomy. Histopathology showed a papillary renal cell carcinoma type 1, with positive immunohistochemical stains for Vimentin, CK7 and AMACR.

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Baby No More: A Rare Case of Papillary Renal Cell Carcinoma in a One Year Old Female

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