膀胱浆母细胞淋巴瘤引起的轻链铸型肾病。

Clinical Nephrology. Case Studies Pub Date : 2021-07-01 eCollection Date: 2021-01-01 DOI:10.5414/CNCS110339
Mehrian Jafarizade, Kiran Goli, Vivette D'Agati, Essel Dulaimi, Krupa Daniel, Bradley Lash, Sharon Maynard
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引用次数: 3

摘要

浆母细胞淋巴瘤(PBL)是一种罕见的b细胞淋巴瘤,常见于潜在免疫抑制的患者,如HIV、自身免疫性疾病和器官移植。hiv阳性患者的PBL通常起源于胃肠道,以口腔为主。PBL累及膀胱极为罕见,由κ轻链分泌PBL引起的铸型肾病也未见报道。病例报告:我们报告了一个病人谁提出了急性肾损伤(AKI)在设置艾滋病毒,并被发现有膀胱肿瘤。膀胱病理显示高级别PBL伴κ轻链限制。肾活检显示κ轻链铸型肾病,可能继发于分泌κ轻链的PBL。结论:虽然PBL的预后很差,但我们的患者从AKI中恢复过来,通过化疗获得了完全的血液学缓解,并成功进行了自体干细胞移植。
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Light chain cast nephropathy caused by plasmablastic lymphoma of the bladder.

Introduction: Plasmablastic lymphoma (PBL) is a rare form of B-cell lymphoma typically seen in patients with underlying immunosuppression such as HIV, autoimmune disease, and organ transplantation. PBL in HIV-positive patients usually originates from the gastrointestinal tract, with a predilection for the oral cavity. Bladder involvement by PBL is exceedingly rare, and cast nephropathy due to κ light chain-secreting PBL has not been reported previously.

Case report: We report a patient who presented with acute kidney injury (AKI) in the setting of HIV, and was found to have a bladder tumor. Bladder pathology revealed a high-grade PBL with κ light chain restriction. Renal biopsy showed κ light chain cast nephropathy, presumably secondary to κ light chain-secreting PBL.

Conclusion: Although the prognosis of PBL is poor, our patient recovered from AKI, achieved complete hematologic remission with chemotherapy, and underwent successful autologous stem cell transplant.

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