Nasr Kristina, Karam Sabine, Mazepa Marshall, Czyzyk Jan, Klomjit Nattawat
Division of Nephrology and Hypertension, Department of Medicine, University of Minnesota, Minneapolis, MN, United States.
Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, MN, United States.
Front Nephrol. 2024 Aug 13;4:1400027. doi: 10.3389/fneph.2024.1400027. eCollection 2024.
Thrombotic microangiopathy (TMA) is a rare renal complication of patients with chronic lymphocytic leukemia (CLL) and is often associated with peripheral features. We present the first case of CLL patients with renal-limited TMA. A 70-year-old female patient with a history of well-controlled type 2 diabetes and baseline albuminuria of 87.2 mg/g 1 year prior and CLL was on active surveillance only. Her baseline white blood cell (WBC) was 202.6 x 10/µl. She presented with nephrotic syndrome with proteinuria of 10 g/g and a subsequent unremarkable serologic work-up. A kidney biopsy revealed diabetic glomerulosclerosis and chronic TMA. Initially, she was treated conservatively with angiotensin receptor blockade and sodium glucose cotransporter-2 inhibition but progressed with increased proteinuria of 17 g/g. Complement functional panel testing was pursued and showed dysregulation of the classical and alternative complement pathways. We decided to treat CLL which was suspected to be the culprit. At 9 months post-ibrutinib initiation, there was a 90% reduction in the WBC as well as a 94% reduction in proteinuria (17 g/g to 0.97 g/g). This case emphasizes the role of complement dysregulation in the pathogenesis of TMA in CLL patients. Treatment of CLL can restore complement dysregulation and improve renal outcomes.
血栓性微血管病(TMA)是慢性淋巴细胞白血病(CLL)患者罕见的肾脏并发症,且常伴有外周表现。我们报告首例局限性肾脏TMA的CLL患者。一名70岁女性患者,有2型糖尿病病史,血糖控制良好,1年前基线白蛋白尿为87.2 mg/g,CLL仅接受主动监测。她的基线白细胞(WBC)为202.6×10⁹/µl。她因肾病综合征就诊,蛋白尿为10 g/g,后续血清学检查无异常。肾脏活检显示糖尿病性肾小球硬化和慢性TMA。最初,她接受了血管紧张素受体阻滞剂和钠-葡萄糖协同转运蛋白2抑制剂的保守治疗,但蛋白尿增加至17 g/g,病情进展。进行了补体功能检测,结果显示经典和替代补体途径失调。我们决定治疗疑似罪魁祸首的CLL。在开始使用伊布替尼9个月后,白细胞减少了90%,蛋白尿减少了94%(从17 g/g降至0.97 g/g)。该病例强调了补体失调在CLL患者TMA发病机制中的作用。治疗CLL可恢复补体失调并改善肾脏预后。