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病例报告:慢性淋巴细胞白血病继发肾局限性血栓性微血管病的成功治疗

Case report: Successful treatment of renal-limited thrombotic microangiopathy secondary to chronic lymphocytic leukemia.

作者信息

Nasr Kristina, Karam Sabine, Mazepa Marshall, Czyzyk Jan, Klomjit Nattawat

机构信息

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.

出版信息

Front Nephrol. 2024 Aug 13;4:1400027. doi: 10.3389/fneph.2024.1400027. eCollection 2024.

DOI:10.3389/fneph.2024.1400027
PMID:39193218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11347436/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11347436/942f720e7129/fneph-04-1400027-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11347436/1f7130d34805/fneph-04-1400027-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11347436/942f720e7129/fneph-04-1400027-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11347436/1f7130d34805/fneph-04-1400027-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abe5/11347436/942f720e7129/fneph-04-1400027-g002.jpg

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本文引用的文献

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Am J Hematol. 2023 Dec;98(12):E369-E372. doi: 10.1002/ajh.27101. Epub 2023 Sep 23.
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A Rare Case of Renal Thrombotic Microangiopathy and Focal Segmental Glomerulosclerosis Secondary to Plasma Cell Leukemia.浆细胞白血病继发肾血栓性微血管病和局灶节段性肾小球硬化1例罕见病例
Case Rep Hematol. 2023 Feb 18;2023:7803704. doi: 10.1155/2023/7803704. eCollection 2023.
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Renal Thrombotic Microangiopathy: A Review.
肾血栓性微血管病:综述。
Am J Kidney Dis. 2023 May;81(5):591-605. doi: 10.1053/j.ajkd.2022.10.014. Epub 2022 Dec 10.
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Diagnosis and treatment of thrombotic microangiopathy.血栓性微血管病的诊断与治疗。
Int J Lab Hematol. 2022 Sep;44 Suppl 1(Suppl 1):101-113. doi: 10.1111/ijlh.13954.
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The prevalence and clinical outcomes of microangiopathic hemolytic anemia in patients with biopsy-proven renal thrombotic microangiopathy.经活检证实的肾血栓性微血管病患者中微血管病性溶血性贫血的患病率及临床结局
Am J Hematol. 2022 Nov;97(11):E426-E429. doi: 10.1002/ajh.26705. Epub 2022 Sep 10.
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Case Report: Chronic Lymphocytic Leukemia With Recurrent Complement-Mediated Thrombotic Microangiopathy and C3 Glomerulonephritis.病例报告:伴复发性补体介导的血栓性微血管病和C3肾小球肾炎的慢性淋巴细胞白血病
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