Bilateral renal cell lymphoma: Case report and review of literature

P. Negi, Harnoor Singh Pruthi, S. Patel, H. Srivastava, M. Kaur, A. Das
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Abstract

Primary renal cell lymphoma is a rare type of non-Hodgkin’s lymphoma, with B-cell lymphoma being the most common subtype. Imaging and preoperative biopsy are fruitful ways to diagnose renal cell lymphoma. We report a rare case of primary renal cell lymphoma with bilateral renal involvement in a 52-year-old woman based on imaging findings, histopathology, and immunohistochemical markers. The patient is being treated with Rituximab, cyclophosphamide, adriamycin, vincristine, prednisolone, and intrathecal methotrexate. Furthermore, the present study also reviewed 22 cases of bilateral PRL that have been reported in this century to date. With this case report, we focus the spotlight on the fact that, though rare, the diagnosis of primary renal cell lymphoma still needs to be in the differential diagnosis of renal masses.
双侧肾细胞淋巴瘤:病例报告及文献复习
原发性肾细胞淋巴瘤是一种罕见的非霍奇金淋巴瘤,其中b细胞淋巴瘤是最常见的亚型。影像学和术前活检是诊断肾细胞淋巴瘤的有效方法。我们报告一例罕见的原发性肾细胞淋巴瘤伴双侧肾脏受累,患者为52岁女性,基于影像学表现、组织病理学和免疫组织化学标记。患者正在接受利妥昔单抗、环磷酰胺、阿霉素、长春新碱、强的松龙和鞘内甲氨蝶呤的治疗。此外,本研究还回顾了本世纪迄今报告的22例双侧PRL病例。通过这个病例报告,我们将焦点放在这样一个事实上:尽管罕见,原发性肾细胞淋巴瘤的诊断仍然需要在肾脏肿块的鉴别诊断中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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