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Primary renal non-Hodgkin's lymphoma presenting as immune thrombocytopenia

机译:原发性肾非霍奇金淋巴瘤表现为免疫性血小板减少

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A 25-year-old man was admitted to our hospital because of hematuria, anemia and thrombocytopenia. Laboratory examinations revealed an increased number of bone marrow megakaryocytes and an increased level of platelet-associated immunoglobulin G, suggesting immune thrombocytopenia. Computed tomography of the abdomen showed enlargement of the bilateral kidneys with multiple low-density areas, although neither lymphadenopathy nor hepatosplenomegaly was evident. After amelioration of the thrombocytopenia by prednisolone therapy, open renal biopsy was performed and a diagnosis of diffuse large B-cell non-Hodgkin's lymphoma was made. The patient achieved complete remission after CHOP therapy. This was thought to be a rare case of primary renal non-Hodgkin's lymphoma initially presenting as immune thrombocytopenia, which was treated successfully by chemotherapy.
机译:一名25岁的男子因血尿,贫血和血小板减少症而入院。实验室检查显示,骨髓巨核细胞数量增加,血小板相关免疫球蛋白G水平升高,提示免疫性血小板减少症。腹部计算机断层扫描显示双侧肾脏肿大,并伴有多个低密度区域,尽管淋巴结肿大和肝脾肿大均无明显意义。通过泼尼松龙治疗改善血小板减少症后,进行了开放性肾活检,并诊断为弥漫性大B细胞非霍奇金淋巴瘤。该患者在CHOP治疗后完全缓解。人们认为这是一例罕见的原发性肾脏非霍奇金淋巴瘤,最初表现为免疫性血小板减少症,已通过化学疗法成功治疗。

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