Open Access
CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2020; 41(02): 264-265
DOI: 10.4103/ijmpo.ijmpo_114_18
Practitioner Section

Primary Neuroendocrine Carcinoma of Kidney: Report of a Rare Case

Sandeep Bhaskar
Department of Radiotherapy, SMS Medical College and Attached Group of Hospitals, Jaipur, Rajasthan, India
,
Kartick Rastogi
Department of Radiotherapy, SMS Medical College and Attached Group of Hospitals, Jaipur, Rajasthan, India
,
Shivani Gupta
Department of Radiotherapy, SMS Medical College and Attached Group of Hospitals, Jaipur, Rajasthan, India
,
Arpita Jindal
Department of Pathology, SMS Medical College and Attached Group of Hospitals, Jaipur, Rajasthan, India
› Author Affiliations

Financial support and sponsorship Nil.
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Abstract

Primary neuroendocrine tumor (NET) of kidney is extremely rare, with <100 cases reported so far. The aim of the present case study is to discuss the clinical and pathological findings of renal NET and review of the available literature. We herein report the case of a 42-year-old female patient, who presented with pain abdomen and hematuria. Immunohistochemistry of her nephrectomy specimen was positive for chromogranin A and CD56 and negative for uroplakin II, P40, and CD10. KI index was 60%. Due to rarity of the tumor, there are no established guidelines available for its treatment. She was treated with combination chemotherapy of cisplatin and etoposide.



Publication History

Received: 14 May 2018

Accepted: 21 June 2018

Article published online:
23 May 2021

© 2020. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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