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

机译:原发性肾非霍奇金的淋巴瘤呈现为免疫血小板减少症

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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:由于血尿,贫血和血小板减少症,一名25岁的男子被院内入院。 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的增加程度,表明免疫血小板减少症。 腹部的计算断层扫描显示,具有多个低密度区域的双侧肾脏的放大,尽管淋巴结病或肝肺组血症都不明显。 通过泼尼松龙治疗改善血小板减少血小阴盆尼亚,进行了开放的肾活组织检查,并进行了弥漫性大B细胞非霍奇金淋巴瘤的诊断。 患者在切碎疗法后取得完全缓解。 这被认为是罕见的肾脏非霍奇金淋巴瘤最初呈现为免疫血小板减少症,其通过化疗成功治疗。

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