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《克隆战争:现代时代的诊断与治疗异常蛋白血症性肾病》

The Clone Wars: Diagnosing and Treating Dysproteinemic Kidney Disease in the Modern Era.

作者信息

Avasare Rupali S, Andeen Nicole K, Havasi Andrea, Hogan Jonathan J

机构信息

Division of Nephrology, Department of Medicine, Oregon Health & Science University, Portland, OR 97239, USA.

Department of Pathology, Oregon Health & Science University, Portland, OR 97239, USA.

出版信息

J Clin Med. 2021 Apr 12;10(8):1633. doi: 10.3390/jcm10081633.

DOI:10.3390/jcm10081633
PMID:33921394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8069250/
Abstract

Dysproteinemic kidney diseases are disorders that occur as the result of lymphoproliferative (B cell or plasma cell) disorders that cause kidney damage via production of nephrotoxic monoclonal immunoglobulins or their components. These monoclonal immunoglobulins have individual physiochemical characteristics that confer specific nephrotoxic properties. There has been increased recognition and revised characterization of these disorders in the last decade, and in some cases, there have been substantial advances in disease understanding and treatments, which has translated to improved patient outcomes. These disorders still present challenges to nephrologists and patients, since they are rare, and the field of hematology is rapidly changing with the introduction of novel testing and treatment strategies. In this review, we will discuss the clinical presentation, kidney biopsy features, hematologic characteristics and treatment of dysproteinemic kidney diseases.

摘要

异常蛋白血症性肾脏疾病是由于淋巴增殖性疾病(B细胞或浆细胞疾病)导致肾损害的疾病,这些疾病通过产生肾毒性单克隆免疫球蛋白或其成分而引起肾脏损伤。这些单克隆免疫球蛋白具有赋予特定肾毒性特性的个体理化特征。在过去十年中,对这些疾病的认识有所增加,其特征也得到了修订,在某些情况下,在疾病理解和治疗方面取得了重大进展,这已转化为患者预后的改善。这些疾病仍然给肾病学家和患者带来挑战,因为它们很罕见,而且随着新型检测和治疗策略的引入,血液学领域正在迅速变化。在本综述中,我们将讨论异常蛋白血症性肾脏疾病的临床表现、肾活检特征、血液学特征和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/4341d3bfd20b/jcm-10-01633-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/3adabb43c12e/jcm-10-01633-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/6ff951905227/jcm-10-01633-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/10dd0f0d835d/jcm-10-01633-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/6fcbbdf64a31/jcm-10-01633-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/eb7a749cf328/jcm-10-01633-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/4341d3bfd20b/jcm-10-01633-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/3adabb43c12e/jcm-10-01633-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/6ff951905227/jcm-10-01633-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/10dd0f0d835d/jcm-10-01633-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/6fcbbdf64a31/jcm-10-01633-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/eb7a749cf328/jcm-10-01633-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8069250/4341d3bfd20b/jcm-10-01633-g007.jpg

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Nephrol Dial Transplant. 2021 Jan 25;36(2):208-215. doi: 10.1093/ndt/gfz176.
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Management of acute kidney injury in symptomatic multiple myeloma.症状性多发性骨髓瘤急性肾损伤的治疗。
Kidney Int. 2021 Mar;99(3):570-580. doi: 10.1016/j.kint.2020.11.010. Epub 2021 Jan 10.
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Kidney transplantation in patients with multiple myeloma: narrative analysis and review of the last two decades.
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Progression of proliferative glomerulonephritis with monoclonal IgG deposits in pediatric patients.儿童患者中伴有单克隆 IgG 沉积的增生性肾小球肾炎的进展。
Pediatr Nephrol. 2021 Apr;36(4):927-937. doi: 10.1007/s00467-020-04763-5. Epub 2020 Oct 12.
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Immunotactoid glomerulopathy is a rare entity with monoclonal and polyclonal variants.免疫触须样肾小球病是一种罕见的疾病,有单克隆和多克隆变异型。
Kidney Int. 2021 Feb;99(2):410-420. doi: 10.1016/j.kint.2020.07.037. Epub 2020 Aug 18.
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Clinically-suspected cast nephropathy: A retrospective, national, real-world study.临床疑诊的 casts 肾病:一项回顾性、全国性、真实世界研究。
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