不仅仅是淀粉样变性:瓦尔登斯特罗姆氏大球蛋白血症相关性肾病的频谱。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Roberta Giachetti, Francesca Ravaglia, Chiara Somma, Claudia Mannucci, Francesco Scaramuzzino, Martina Rousseau, Silvia Birtolo
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引用次数: 0

摘要

Waldenström巨球蛋白血症(WM)的肾脏受累是一种罕见但临床上重要的并发症,通常在科学文献中未被充分认识和描述。当肾脏损害发生时,它会对患者的预后和肾脏预后产生负面影响,因此突出了早期识别和靶向治疗的重要性。虽然b细胞定向治疗是至关重要的,但治疗策略仍然是非标准化的,并且许多现有文献早于布鲁顿酪氨酸激酶(BTK)抑制剂的广泛使用。在这篇文章中,我们报告了一个用第二代BTK抑制剂zanubrutinib成功治疗wm相关重、轻链沉积病的病例,强调了新型靶向药物在这种情况下的潜在作用。此外,我们提供了一个简短的回顾肾脏并发症与WM和讨论一些治疗注意事项。然而,现有的数据是异构的,不足以得出关于临床结果和特定治疗策略之间关系的明确结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Not just amyloidosis: the spectrum of Waldenstrom's macroglobulinemia-associated renal disease.

Renal involvement in Waldenström's macroglobulinemia (WM) is a rare but clinically significant complication that is often underrecognized and inadequately described in the scientific literature. When kidney damage occurs, it negatively impacts both patient prognosis and renal outcomes, highlighting the importance of early recognition and targeted therapy. While B-cell directed treatment is crucial, therapeutic strategies remain non-standardized, and much of the existing literature predates the widespread use of Bruton's tyrosine kinase (BTK) inhibitors. In this manuscript, we present a case of WM-associated heavy and light chain deposition disease successfully treated with the second-generation BTK inhibitor zanubrutinib, emphasizing the potential role of novel targeted agents in this setting. Additionally, we provide a brief review of renal complications associated with WM and discuss some therapeutic considerations. However, the available data are heterogeneous and insufficient to draw definitive conclusions regarding the relationship between clinical outcomes and specific treatment strategies.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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