Törnroth T, Honkanen E, Pettersson E
Fourth Department of Medicine, Helsinki University Central Hospital, Finland.
Clin Nephrol. 1987 Sep;28(3):107-17.
Membranous glomerulonephritis (MGN) has a highly variable clinical course. The morphological basis for this variability has not been fully elucidated. We studied 10 patients with relapsing MGN and compared the findings with those in other clinical courses. The mean duration of follow-up was 10.4 years. Clinical remission occurred, on average, 1.5 years and relapse, on average, 5.6 years after onset. Thirty-one renal biopsies obtained at various clinical phases were studied, 22 of them electron microscopically. The ultrastructural and clinical alterations paralleled each other closely. Subepithelial electron-dense deposits were present during the primary nephrotic phase, were replaced by intramembranous lucent deposits during remission, and reappeared again during relapse. Light microscopic changes (projections, thickening) of the glomerular capillary basement membrane (GBM) were variable. Both ultrastructural and light microscopic changes were unreliable indicators of the duration of illness. A comparative analysis of the present and previous findings suggests that the length of time during which new deposit material is formed determines the evolution of the membranous lesion and the corresponding clinical course. Thus, a short duration results in a single generation of deposits, a morphologically and clinically healing course, and no thickening of the GBM. A repeated formation of deposit material results in a new generation of subepithelial deposits, and a relapsing course. A prolonged formation results in a continuous presence of subepithelial deposits, a thickening of the GBM, and a protracted or progressive course. The morphologic staging currently in use pertains to one particular evolution and course of MGN and therefore should not be used.
膜性肾小球肾炎(MGN)的临床病程高度可变。这种变异性的形态学基础尚未完全阐明。我们研究了10例复发性MGN患者,并将研究结果与其他临床病程的患者进行比较。平均随访时间为10.4年。临床缓解平均发生在起病后1.5年,复发平均发生在起病后5.6年。我们研究了在不同临床阶段获取的31份肾活检标本,其中22份进行了电子显微镜检查。超微结构改变与临床改变密切平行。上皮下电子致密沉积物在原发性肾病阶段出现,在缓解期被膜内透明沉积物取代,并在复发期再次出现。肾小球毛细血管基底膜(GBM)的光镜改变(凸起、增厚)各不相同。超微结构和光镜改变均不是疾病持续时间的可靠指标。对当前和既往研究结果的比较分析表明,新沉积物形成的时间长度决定了膜性病变的演变及相应的临床病程。因此,短时间形成导致单代沉积物、形态学和临床上的愈合病程以及GBM无增厚。沉积物材料的反复形成导致新一代上皮下沉积物及复发病程。长时间形成导致上皮下沉积物持续存在、GBM增厚以及病程迁延或进展。目前使用的形态学分期适用于MGN的一种特定演变和病程,因此不应使用。