CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2017; 38(04): 545-547
DOI: 10.4103/ijmpo.ijmpo_167_16
Case Report

Primary Renal Cell Lymphoma: Case Report, Diagnosis, and Management

Rajat Thawani
Internal Medicine, Maimonides Medical Center, Brooklyn, NY,
,
Amarendra Amar
Department of Hematology and Oncology, Indraprastha Apollo Hospitals, New Delhi, India
,
Jayanta Patowary
Department of Hematology and Oncology, Indraprastha Apollo Hospitals, New Delhi, India
,
Sumaid Kaul
Department of Pathology, Indraprastha Apollo Hospitals, New Delhi, India
,
Amarnath Jena
Department of Nuclear Medicine, Indraprastha Apollo Hospitals, New Delhi, India
,
Pratap Das
Department of Hematology and Oncology, Indraprastha Apollo Hospitals, New Delhi, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

The symptoms of primary renal lymphoma (PRL) may mimic a renal cell carcinoma. Since the diagnosis is mostly after a radical nephrectomy, we recommend a percutaneous biopsy or cytology from the renal mass in patients who have features suggestive of a lymphoma. A magnetic resonance imaging may give an image more specific for a lymphoma. There are no clinical trials for the treatment of PRL, but all previously published case reports used R-CHOP and a few patients did better than the median survival of 6 months.



Publication History

Article published online:
04 July 2021

© 2017. 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 forcommercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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