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移植肾的膜性肾小球肾炎(MGN):对256例同种异体肾移植的形态学研究

Membranous glomerulonephritis (MGN) in transplanted kidneys: morphologic investigation on 256 renal allografts.

作者信息

Monga G, Mazzucco G, Basolo B, Quaranta S, Motta M, Segoloni G, Amoroso A

机构信息

Department of Biomedicine and Human Oncology, University of Torino, Italy.

出版信息

Mod Pathol. 1993 May;6(3):249-58.

PMID:8346172
Abstract

Twenty-two cases of membraneous glomerulonephritis (MGN) were identified among 256 bioptically investigated transplanted patients. MGN was defined as de novo in 15 patients and recurrent in three. The type of MGN could not be ascertained with certainty in the other four. Several morphologic features unusual for the idiopathic form of MGN were found. Most cases disclosed focal segmental distribution of subepithelial deposits and showed the contemporaneous presence of different stages of the disease according to Ehrenreich and Churg classification. In addition mild-to-moderate mesangial cell proliferation was found in about one third of de novo MGN biopsies. Endocapillary hypercellularity was observed in 14 specimens and held to be due to an excess of mononuclear blood cells, related to a concomitant episode of rejection. Chronic transplant glomerulopathy was found in 47% of patients with de novo MGN and in 66% of those with recurrent MGN, being more frequently observed in specimens with diffuse distribution of deposits. Repeated biopsies showed progression of the stage and extension of deposits to a large number of capillary loops in four out of six patients. De novo MGN was documented 1 to 54 mo (mean value 20.2 mo) after transplantation, and the recurrence was observed after 12, 15, and 42 mo. All but two patients (who were anuric) complained of proteinuria, which was in the nephrotic range in 12. Apart from the significantly higher frequency in de novo MGN patients of DR4 antigen, whose significance must in any case be re-evaluated in a larger series, none of the factors so far suggested to be linked to the onset of de novo MGN has found further support in our study. On the contrary, relevance in favoring the appearance and the evolution of MGN has to be attributed to transplant glomerulopathy, which, moreover, seems to be more important than MGN itself in causing the unfavorable outcome of the graft.

摘要

在256例接受活检的移植患者中,确诊了22例膜性肾小球肾炎(MGN)。其中15例MGN被定义为新发,3例为复发。另外4例的MGN类型无法明确确定。发现了一些对于特发性MGN而言不寻常的形态学特征。大多数病例显示上皮下沉积物呈局灶节段性分布,并根据埃伦赖希和丘格分类法呈现疾病不同阶段的同时存在。此外,约三分之一的新发MGN活检标本中发现了轻度至中度的系膜细胞增殖。14份标本中观察到毛细血管内细胞增多,认为这是由于单核血细胞过多所致,与同时发生的排斥反应有关。47%的新发MGN患者和66%的复发MGN患者出现慢性移植肾小球病,在沉积物弥漫分布的标本中更常观察到。6例患者中有4例重复活检显示疾病阶段进展以及沉积物扩展至大量毛细血管袢。新发MGN在移植后1至54个月(平均20.2个月)被记录,复发分别在12、15和42个月后被观察到。除两名无尿患者外,所有患者均有蛋白尿主诉,其中12例蛋白尿处于肾病范围。除了新发MGN患者中DR4抗原频率显著更高(其意义无论如何都必须在更大系列中重新评估)外,迄今为止提出的与新发MGN发病相关的因素在我们的研究中均未得到进一步支持。相反,必须将有利于MGN出现和进展的相关性归因于移植肾小球病,而且,移植肾小球病在导致移植物不良结局方面似乎比MGN本身更重要。

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