• Sonuç bulunamadı

Clinical features of thin basement membrane disease and associated glomerulopathies.

N/A
N/A
Protected

Academic year: 2021

Share "Clinical features of thin basement membrane disease and associated glomerulopathies."

Copied!
1
0
0

Yükleniyor.... (view fulltext now)

Tam metin

(1)

Clinical features of thin basement membrane disease

and associated glomerulopathies.

蘇裕謀

Sue YM;Huang JJ;Hsieh RY;Chen FF

摘要

Abstract

Background: Thin basement membrane disease (TBMD) occurs in 5–11% of renal biopsy series, and can be associated with other glomerulopathies (GNs). Data on the prevalence, clinical features, and prognosis of TBMD with other GNs are limited.

Methods and Results: From June 1990 to May 2001, findings from 658 native kidney biopsies were retrospectively studied. The overall prevalence of TBMD was 7.9% (52 of 658). The mean glomerular basement membrane (GBM) thickness was 206 ± 30 nm. Clinicopathological features were compared for patients with TBMD only (n = 14) and in those with TBMD and GN (n = 38). Focal segmental

glomerulosclerosis, mesangial proliferative GN, and minimal change disease were the most common GNs associated with TBMD. After a mean follow-up period of 44.9 ± 42.5 months, the group who only had TBMD revealed a relatively benign disease with microscopic haematuria and trivial proteinuria, a low prevalence of hypertension, and no renal progression. In the group who had both TBMD and GN, heavy proteinuria (6.1 ± 5.2 g/day), hypoalbuminaemia (26 ± 12 g/L) and renal insufficiency (76 ± 25 mL/min) might develop.

Conclusion: We suggested that the TBMD is a developmental abnormality of little or no significance and that it is the underlying associated GN rather than TBMD, which has the relevance to the outcome of renal disease

. .

Referanslar

Benzer Belgeler

Initially she was treated with PAIR for liver disease but surgery was necessary due to con- tinued high serological titres and the presence of a uni- locular cyst, which was

In this report, a ten month- old girl with prolonged fever, aseptic meningi- tis and facial palsy who later diagnosed as Kawasaki disease was described and also the clinical

Therapeu- tic angiogenesis in Buerger’s disease (thromboangiitis obliterans) patients with critical limb ischemia by autologous transplantation of bone marrow mononuclear

In conclusion, the results of this study demonstrated that low plasma HDL levels and high hs CRP levels measured inde- pendently of endothelial functions of patients with PAD are risk

The present study aimed to examine serum activin A levels under different coronary clinical presentations [ST-segment el- evation myocardial infarction (STEMI), non-STEMI (NSTEMI),

Objective: The present study aimed to investigate the association between the rs10757274 SNP (present on locus 9p21 in the gene for CDKN2B- AS1) and coronary artery disease (CAD) in

In this report, we describe the clinical features, and follow-up of eight patients with incomplete Kawasaki disease complicated with coronary artery abnormalities.. Patients

Adverse clinical outcomes including death, pulmonary edema, and valvular interventions were frequent among patients with severe VHD, whereas no adverse clini- cal outcome was