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基于组织形态计量学研究的晚发性巨肾小球病的病理和临床特征。

Pathological and clinical characteristics of late-onset oligomeganephronia based on a histomorphometric study.

机构信息

Laboratory of Electron Microscopy, Pathological Center, Peking University First Hospital, No. 8, Xishiku Street, Beijing, 100034, People's Republic of China.

Renal Division, Department of Medicine, Institute of Nephrology, Key Laboratory of Renal Disease, Key Laboratory of CKD Prevention and Treatment, Peking University First Hospital, Peking University, Ministry of Health of China, Ministry of Education of China, Beijing, People's Republic of China.

出版信息

BMC Nephrol. 2023 Mar 15;24(1):54. doi: 10.1186/s12882-023-03096-3.

Abstract

BACKGROUND

Late-onset oligomeganephronia (OMN) is a rare chronic kidney disease and has no quantitative criteria for diagnosis yet. The current study aimed to explore its clinicopathological features by histomorphometric analysis.

METHODS

We retrospectively re-reviewed all patients with enlarged and sparse glomeruli by light microscopy at Peking University First Hospital from 2012 to 2021, excluding those with any factor known to contribute to similar changes. Age- and sex-matched patients with thin basement membrane nephropathy were selected as control to establish the cut-off values for glomerulomegaly and rarity. Late-onset OMN cases were then confirmed and the clinicopathological characteristics were summarized.

RESULTS

Mean diameter and density of cortical glomeruli in control was 156.53 ± 27.50 μm and 4.07 ± 0.63 /mm, giving a lower limit of 211.53 μm for glomerulomegaly and an upper of 2.81 /mm for rarity. Seven adults of three females and four males were finally diagnosed as late-onset OMN with a mean age of 26.57 years. They showed mild to moderate proteinuria and/or renal dysfunction at biopsy with the mean proteinuria, serum creatinine (Scr) level, and estimated glomerular filtration rate of 0.50 g/d (0.10-0.95 g/d), 140.9 µmol/L (95.1-227.1 µmol/L), and 58.7 mL/min/1.73m (21.3-98.0 mL/min/1.73m), respectively. Four patients (57.1%) had normal Scr at diagnosis. Six patients with available data showed renal tubular injury with increased urinary microalbumin in all, elevated N-acetyl-β-glucosaminidase in two, and elevated α1 microglobulin in five. Kidney size was normal or slightly reduced. The mean density and glomerular diameter of the seven cases was 0.86 mm (0.55-1.41 /mm) and 229.73 μm (211.88-260.66 μm). Segmental glomerular sclerosis was observed in six (85.7%) with four (66.7%) of perihilar type. Proximal tubule dilation was observed in all, focal to diffuse, lining with enlarged epithelial cells. The mean foot process width was 634.02 nm, wider than 472.54 nm of the control (P = 0.0002).

CONCLUSION

Late-onset OMN should be considered a special entity with relatively slow clinical progress characterized by hypertrophy of the sparsely distributed nephron.

摘要

背景

迟发性巨肾小球病(OMN)是一种罕见的慢性肾脏疾病,目前尚无明确的诊断定量标准。本研究旨在通过组织形态计量学分析探讨其临床病理特征。

方法

我们回顾性地重新审查了 2012 年至 2021 年期间北京大学第一医院因光镜检查显示肾小球增大和稀疏而就诊的所有患者,排除了任何已知可导致类似改变的因素。选择年龄和性别匹配的薄基底膜肾病患者作为对照,建立肾小球肥大和稀疏的截断值。然后确认迟发性 OMN 病例,并总结其临床病理特征。

结果

对照组肾小球的平均直径和密度分别为 156.53±27.50μm 和 4.07±0.63 /mm,肾小球肥大的下限为 211.53μm,稀疏的上限为 2.81 /mm。最终确诊了 7 例成年患者,3 例为女性,4 例为男性,平均年龄为 26.57 岁。他们在活检时表现为轻至中度蛋白尿和/或肾功能障碍,平均蛋白尿、血清肌酐(Scr)水平和估算肾小球滤过率分别为 0.50g/d(0.10-0.95g/d)、140.9μmol/L(95.1-227.1μmol/L)和 58.7mL/min/1.73m(21.3-98.0mL/min/1.73m)。4 例患者(57.1%)在诊断时 Scr 正常。6 例有可用数据的患者均显示肾小管损伤,所有患者尿微量白蛋白增加,2 例患者 N-乙酰-β-氨基葡萄糖苷酶升高,5 例患者α1 微球蛋白升高。肾脏大小正常或略小。7 例患者的平均密度和肾小球直径分别为 0.86mm(0.55-1.41 /mm)和 229.73μm(211.88-260.66μm)。6 例(85.7%)患者观察到节段性肾小球硬化,其中 4 例(66.7%)为门部纤维化。所有患者均存在近端肾小管扩张,从局灶性到弥漫性,衬有增大的上皮细胞。平均足突宽度为 634.02nm,宽于对照组的 472.54nm(P=0.0002)。

结论

迟发性 OMN 应被视为一种特殊实体,其临床进展相对缓慢,特征为稀疏分布的肾单位肥大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9674/10018837/14b88de7273b/12882_2023_3096_Fig1_HTML.jpg

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