瓦尔登斯特罗姆大球蛋白血症患者肾脏的淋巴瘤浸润。

Prasanth Ravipati, Lihong Bu, Zohar Sachs, Patrick H Nachman
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摘要

肾脏疾病可以是浆细胞异常的初始表现或慢性表现。在此,我们报告一例罕见的由肾脏淋巴瘤浸润引起的肾脏疾病,患者为华氏巨球蛋白血症(WM)。一位70岁女性,有8年的WM (IgM, κ)病史,因肾功能下降而入院。在发病前,她有稳定的WM疾病,没有疾病负担加重的证据。她曾因SARS-CoV-2感染和急性肾损伤(AKI)住院。她的血清肌酐(sCr)峰值为3.7 mg/dL(基线为0.9 mg/dL),但在出院时恢复到1.1 mg/dL。出院2个月后sCr升高至1.9 mg/dL,新增蛋白尿1.5 g/d。肾活检显示间质有淋巴瘤浸润,未累及肾小球。利妥昔单抗和苯达莫司汀治疗导致肾功能改善(sCr 1.4 mg/dL)。WM是一种罕见的血液恶性肿瘤,髓外受累,包括肾脏受累,是罕见的。本病例强调了监测浆细胞异常患者肾功能障碍的重要性,即使患者表现为稳定的淋巴细胞增生性疾病。
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Lymphomatous infiltration of the kidney in a patient with Waldenstrom's macroglobulinemia.

Kidney disease can be an initial presentation or a chronic manifestation of plasma cell dyscrasias. Here, we describe a rare presentation of kidney disease driven by lymphomatous infiltration of the kidney in a patient with Waldenstrom's macroglobulinemia (WM). A 70-year-old female with an 8-year history of WM (IgM, κ) was referred for declining renal function. Prior to presentation, she had stable WM disease without evidence of worsening disease burden. She had been previously hospitalized with SARS-CoV-2 infection and acute kidney injury (AKI). Her serum creatinine (sCr) peaked at 3.7 mg/dL (baseline 0.9 mg/dL) but recovered to 1.1 mg/dL by the time of discharge. Two months after discharge, her sCr increased to 1.9 mg/dL, and she had new proteinuria of 1.5 g/day. Kidney biopsy showed lymphomatous infiltration of the interstitium without glomerular involvement. Treatment with rituximab and bendamustine resulted in an improvement in renal function (sCr 1.4 mg/dL). WM is an uncommon hematologic malignancy, and extramedullary involvement, including renal involvement, is rare. This case emphasizes the importance of surveillance for kidney dysfunction in patients with plasma cell dyscrasias, even if patients appear to have stable lymphoproliferative disease.

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