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Teenager with a Primary Renal Lymphoma: A Case Report

机译:少年有原发性肾淋巴瘤:案例报告

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We report a case of an 18-year-old male patient who was diagnosed with primary renal lymphoma (PRL) through biopsy findings and imaging studies. The patient presented with clinical manifestations of distal renal tubular acidosis including polyuria, polydipsia, lower limb weakness, involuntary weight loss, asthenia and dyspnea. No personal background or relevant medical history was reported. A kidney biopsy showed high grade immature B-cell lymphoproliferative process (Non-Hodgkin's Lymphoma) with a Ki67 value greater than 90%. Complementary studies excluded primary lymphoid migration sites, which confirmed the diagnosis of PRL. The oncology unit initiated treatment with a combination of medications due to lack of protocols for the specific treatment. Besides the fact that this condition is rare, it also shows a unique symptoms presentation and non-typical findings in imaging methods. Also, it is important to underline the fact that the treatment is not yet specified for such type of cancer and different combinations are needed to control the disease.
机译:我们举报了一个18岁的男性患者,通过活组织检查发现和成像研究被诊断出患有原发性肾淋巴瘤(PRL)。患者患有远端肾小管酸中毒的临床表现,包括聚尿,较柔软潜水员,下肢弱点,无意重的减肥,哮喘和呼吸困难。没有报告个人背景或相关病史。肾脏活检显示出高级未成熟的B细胞淋巴抑制过程(非霍奇金淋巴瘤),ki67值大于90%。互补研究排除了主要淋巴迁移位点,证实了PRL的诊断。肿瘤学单位由于缺乏特定治疗的方案而导致治疗药物的组合。除了这种情况罕见的事实,它还显示了成像方法的独特症状呈现和非典型发现。此外,强调尚未针对这种类型的癌症指定治疗和不同组合来控制疾病的事实是重要的。

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