Eddy A, Sibley R, Mauer S M, Kim Y
Clin Nephrol. 1984 Jun;21(6):305-13.
Dense intramembranous deposit disease (DIDD) almost universally recurs in renal allografts. However, the 29 previously reported cases suggest that recurrent DIDD rarely results in graft failure. We studied the clinical course and renal histology of the 6 patients with DIDD who have received renal allografts here since 1967. All patients had characteristic findings of DIDD in their native kidneys by light, immunofluorescence and electron microscopy. Seven grafts in 4 patients failed and histological evaluation showed that 5 of these allografts in 4 patients were lost due to recurrent disease. They all demonstrated marked mesangial proliferation with crescents but minimal acute interstitial or vascular changes of rejection. Patients with graft failure due to recurrent disease were male and developed recurrent nephrotic syndrome. The 2 patients with rapidly progressive glomerulonephritis (RPGN) in their native kidneys lost the transplanted kidney due to recurrent disease within 1 year. This study suggests that recurrence of DIDD in renal allografts is a more serious problem than previously appreciated, especially in patients with RPGN.
致密内皮下沉积病(DIDD)在肾移植中几乎普遍复发。然而,先前报道的29例病例表明,复发性DIDD很少导致移植肾失败。我们研究了自1967年以来在此接受肾移植的6例DIDD患者的临床病程和肾脏组织学。所有患者通过光镜、免疫荧光和电镜检查在其自身肾脏中均有DIDD的特征性表现。4例患者的7个移植肾失败,组织学评估显示,这4例患者中的5个移植肾因复发性疾病而丧失。它们均表现为明显的系膜增生伴新月体形成,但急性间质或血管排斥反应变化轻微。因复发性疾病导致移植肾失败的患者为男性,并出现复发性肾病综合征。其自身肾脏患有快速进展性肾小球肾炎(RPGN)的2例患者在1年内因复发性疾病而失去了移植肾。这项研究表明,肾移植中DIDD的复发是一个比以前认识到的更为严重的问题,尤其是在患有RPGN的患者中。