单克隆轻链("骨髓瘤")铸型肾病的特征与免疫荧光挑战,重点是电子显微镜。

IF 1.1 4区 医学 Q4 MICROSCOPY Ultrastructural Pathology Pub Date : 2024-09-02 Epub Date: 2024-08-21 DOI:10.1080/01913123.2024.2390892
Guillermo A Herrera, Luan D Truong, Sadhna Dhingra, Elba A Turbat-Herrera
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引用次数: 0

摘要

肾脏疾病是浆细胞异常患者发病和死亡的常见原因。无血清轻链测定可用于不明原因的急性肾损伤患者(多为老年人),以筛查潜在的骨髓瘤铸型肾病。本研究对骨髓瘤铸型肾病的诊断特征进行了系统回顾。目前尚未对多发性骨髓瘤患者肾小管铸型的形态特征进行系统分析。本研究重点研究了一系列 23 例轻链("骨髓瘤")铸型肾病患者的这些铸型的形态,强调了超微结构特征,并将其与 10 例不同疾病患者的铸型进行了比较。免疫荧光数据与形态学结果相互关联,从而提供诊断评估和实践指南。经鉴定,可诊断骨髓瘤相关铸型肾病的超微结构特征包括:铸型中的淀粉样蛋白和结晶、多个界限清晰的断裂面形成铸型内容物的复杂拼图排列(表明相关免疫球蛋白轻链的脆性),以及反应性小管细胞与铸型肾病患者的肾小管相衬。在 95.2% 的 MCN 病例中出现了这些特征,而在其他肾脏疾病中却没有出现这些铸型。在相当大比例的 MCN 病例中,骨髓瘤铸型表现出轻链单克隆性,而且通常没有 IgA 或 IgM 染色。与此相反,大多数非骨髓瘤铸型都对 kappa 和 lambda 轻链、lgA 和 lgM 进行了染色,并在超微结构上显示出相当均匀的细粒至粗粒电子密度,偶尔会混有细胞碎片。
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Features that characterize monoclonal light chain ("myeloma") cast nephropathy with immunofluorescence challenges and emphasis on electron microscopy.

Renal disease is a common cause of morbidity and mortality in patients with plasma cell dyscrasias. The serum-free light chain assay is used in patients, mostly older, with unexplained acute kidney injury to screen for potential myeloma cast nephropathy. This study consists of a systematic review of diagnostic features in myeloma cast nephropathy. The morphological features of tubular casts in patients with multiple myeloma have not been systematically analyzed. This study focuses on the morphology of these casts, emphasizing ultrastructural features, in a series of 23 patients with light chain ("myeloma") cast nephropathy and compared them with casts in 10 patients with various diseases. The immunofluorescence data were correlated with morphological findings to provide diagnostic assessments and practice guidelines. The ultrastructural features identified as diagnostic of casts associated with myeloma included: amyloid and crystals in the casts, multiple well-defined fracture planes forming a complex jigsaw puzzle arrangement of cast contents, indicative of the fragility of the immunoglobulin light chains involved, and reactive tubular cells lining the tubules with the casts. These features were seen in 95.2% of MCN cases and none of the casts in other renal conditions. Myeloma casts exhibited light chain monoclonality in a significant percentage of the MCN cases and often no staining for IgA or IgM. In contrast, the majority of non-myeloma casts stained for both kappa and lambda light chains, lgA, and lgM, and showed ultrastructurally a rather uniform finely to coarsely granular electron density occasionally admixed with cellular debris.

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来源期刊
Ultrastructural Pathology
Ultrastructural Pathology 医学-病理学
CiteScore
2.00
自引率
10.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: Ultrastructural Pathology is the official journal of the Society for Ultrastructural Pathology. Published bimonthly, we are the only journal to be devoted entirely to diagnostic ultrastructural pathology. Ultrastructural Pathology is the ideal journal to publish high-quality research on the following topics: Advances in the uses of electron microscopic and immunohistochemical techniques Correlations of ultrastructural data with light microscopy, histochemistry, immunohistochemistry, biochemistry, cell and tissue culturing, and electron probe analysis Important new, investigative, clinical, and diagnostic EM methods.
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