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多发性骨髓瘤相关轻链淀粉样变性及单克隆免疫球蛋白相关肾病的一种拟议方法

Multiple Myeloma-Associated Light Chain Amyloidosis and a Proposed Approach to Monoclonal Immunoglobulin-Associated Renal Disease.

作者信息

Chang Zi Yun, Thamboo Thomas Paulraj, Choong Clarice Shi Hui, Wong Weng Kin, Ngoh Clara Lee Ying

机构信息

Department of Medicine, National University Health System, Singapore, Singapore.

Department of Pathology, National University Heath System, Singapore, Singapore.

出版信息

Case Rep Nephrol Dial. 2020 Sep 11;10(3):95-103. doi: 10.1159/000508785. eCollection 2020 Sep-Dec.

DOI:10.1159/000508785
PMID:33083386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7548845/
Abstract

Many challenges remain in diagnosing monoclonal immunoglobulin-associated renal disease, despite widespread application of immunofluorescence (IF) and immunohistochemistry. Here, we report a newly diagnosed case of multiple myeloma with clinical suspicion of renal amyloidosis, which had negative IF staining for kappa and lambda light chains in the glomeruli. Although laser microdissection and mass spectrometry-based proteomic analysis have emerged as important tools for amyloid typing in the literature, such facilities are still not widely available in Asia. We propose that a clinicopathological algorithm for the evaluation of organized monoclonal renal deposits, together with a combined nephrological-haematological approach, will still be adequate to generate an unequivocal diagnosis in the majority of cases.

摘要

尽管免疫荧光(IF)和免疫组织化学已广泛应用,但在诊断单克隆免疫球蛋白相关肾病方面仍存在许多挑战。在此,我们报告一例新诊断的多发性骨髓瘤病例,临床怀疑为肾淀粉样变性,其肾小球κ和λ轻链的IF染色为阴性。虽然激光显微切割和基于质谱的蛋白质组分析在文献中已成为淀粉样蛋白分型的重要工具,但此类设备在亚洲仍未广泛应用。我们提出,用于评估有组织的单克隆肾沉积物的临床病理算法,结合肾脏-血液学联合方法,在大多数病例中仍足以做出明确诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/112a20d5c0f0/cnd-0010-0095-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/cb7d65099aaf/cnd-0010-0095-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/283e59aff5cd/cnd-0010-0095-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/112a20d5c0f0/cnd-0010-0095-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/cb7d65099aaf/cnd-0010-0095-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/283e59aff5cd/cnd-0010-0095-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2da9/7548845/112a20d5c0f0/cnd-0010-0095-g03.jpg

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Multiple Myeloma-Associated Light Chain Amyloidosis and a Proposed Approach to Monoclonal Immunoglobulin-Associated Renal Disease.多发性骨髓瘤相关轻链淀粉样变性及单克隆免疫球蛋白相关肾病的一种拟议方法
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本文引用的文献

1
DNAJB9-positive monotypic fibrillary glomerulonephritis is not associated with monoclonal gammopathy in the vast majority of patients.在绝大多数患者中,DNAJB9阳性单型纤维性肾小球肾炎与单克隆丙种球蛋白病无关。
Kidney Int. 2020 Aug;98(2):498-504. doi: 10.1016/j.kint.2020.02.025. Epub 2020 Mar 28.
2
The evaluation of monoclonal gammopathy of renal significance: a consensus report of the International Kidney and Monoclonal Gammopathy Research Group.肾脏意义单克隆丙种球蛋白病的评估:国际肾脏病和单克隆丙种球蛋白病研究小组的共识报告。
Nat Rev Nephrol. 2019 Jan;15(1):45-59. doi: 10.1038/s41581-018-0077-4.
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The Complexity and Heterogeneity of Monoclonal Immunoglobulin-Associated Renal Diseases.
单克隆免疫球蛋白相关肾脏疾病的复杂性和异质性。
J Am Soc Nephrol. 2018 Jul;29(7):1810-1823. doi: 10.1681/ASN.2017121319. Epub 2018 Apr 27.
4
DNAJB9 Is a Specific Immunohistochemical Marker for Fibrillary Glomerulonephritis.DNAJB9是纤维性肾小球肾炎的一种特异性免疫组织化学标志物。
Kidney Int Rep. 2017 Aug 8;3(1):56-64. doi: 10.1016/j.ekir.2017.07.017. eCollection 2018 Jan.
5
Progression of Monoclonal Gammopathy with Undetermined Significance to Multiple Myeloma Diagnosed by Kidney Biopsy: A Case Report.经肾活检诊断意义未明的单克隆丙种球蛋白病进展为多发性骨髓瘤:一例报告
Case Rep Nephrol Dial. 2015 Sep 2;5(3):180-6. doi: 10.1159/000439267. eCollection 2015 Sep-Dec.
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Membranoproliferative glomerulonephritis with masked monotypic immunoglobulin deposits.伴隐匿性单型免疫球蛋白沉积的膜增生性肾小球肾炎
Kidney Int. 2015 Oct;88(4):867-73. doi: 10.1038/ki.2015.195. Epub 2015 Jul 8.
7
Amyloid nephropathy.淀粉样肾病
Clin Kidney J. 2014 Apr;7(2):97-106. doi: 10.1093/ckj/sfu021. Epub 2014 Mar 13.
8
Diagnosis of monoclonal gammopathy of renal significance.肾脏相关意义单克隆丙种球蛋白血症的诊断。
Kidney Int. 2015 Apr;87(4):698-711. doi: 10.1038/ki.2014.408. Epub 2015 Jan 21.
9
Renal amyloidosis: origin and clinicopathologic correlations of 474 recent cases.肾脏淀粉样变性:474 例近期病例的起源和临床病理相关性。
Clin J Am Soc Nephrol. 2013 Sep;8(9):1515-23. doi: 10.2215/CJN.10491012. Epub 2013 May 23.
10
Laser microdissection and mass spectrometry-based proteomics aids the diagnosis and typing of renal amyloidosis.激光显微切割和基于质谱的蛋白质组学有助于肾淀粉样变性的诊断和分型。
Kidney Int. 2012 Jul;82(2):226-34. doi: 10.1038/ki.2012.108. Epub 2012 Apr 11.