Why the study?
Primary renal lymphoma is an exceedingly rare entity, and published medical literature regarding its natural history and clinical outcomes remains limited.
Primary renal lymphoma is an exceedingly rare entity requiring a high index of suspicion for timely diagnosis and treatment.
Warrants inclusion in differentials for atypical renal masses; literature review leaves optimal management open.
Primary renal lymphoma (PRL) is defined as a non-Hodgkin's lymphoma restricted to kidneys with the absence of extensive nodal disease. It is an exceedingly rare clinicopathological entity, accounting for 0.7% of extranodal lymphomas. Published medical literature regarding the natural history and clinical outcomes of PRL remains limited. We describe a case of a young patient who presented with left shoulder pain, continuous fever, and unexplained weight loss as atypical initial manifestations of bilateral PRL, confirmed with the standard set of investigations. Furthermore, this article reviews the literature and discusses various aspects of PRL, including pathophysiology, presentation patterns, imaging and pathological characteristics, management, and prognosis. This paper serves to provide an update and aims to enhance the understanding of PRL. Timely diagnosis and treatment are imperative to achieve improved outcomes. Clinicians should maintain a high index of suspicion in order to prevent morbidity and mortality associated with this serious disease.
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Bokhari et al. (2020) studied this question.
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