Literature DB >> 2129468

Clinicopathological features in patients with isolated C3 mesangial proliferative glomerulonephritis.

C Manno1, A R Proscia, E Laraia, M Giangrande, M Di Carlo, C Salvatore, A Tasco, F P Schena.   

Abstract

The clinicopathological picture of 'isolated C3 mesangial nephritis' was studied in our case records. Focal and segmental or generalised deposits of C3 in the mesangium were found in 12 of 157 (7.6%) patients with primary glomerulonephritis. The clinical picture, similar to Berger's disease, was characterised by episodes of gross haematuria and/or persistent or recurrent microhaematuria and/or proteinuria. Arterial hypertension and mild renal failure were observed in one case. Light-microscopy showed minor glomerular changes such as focal and segmental increase of mesangial matrix and mesangial hyperplasia. During the short-term follow-up (median 25.5 months) no deterioration of renal function was observed. The clinical course and short-term prognosis suggest that this form of glomerulonephritis is benign.

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Year:  1990        PMID: 2129468     DOI: 10.1093/ndt/5.suppl_1.78

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  3 in total

1.  Clinicopathologic features, outcome, and therapeutic interventions in four children with isolated C3 mesangial proliferative glomerulonephritis.

Authors:  Kazuro Yagi; Hidehiko Yanagida; Keisuke Sugimoto; Hiroaki Kuwajima; Nobutada Tabata; Kosuke Morita; Mitsuru Okada; Tsukasa Takemura
Journal:  Pediatr Nephrol       Date:  2005-06-10       Impact factor: 3.714

2.  Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees.

Authors:  Yiannis Athanasiou; Konstantinos Voskarides; Daniel P Gale; Loukas Damianou; Charalambos Patsias; Michalis Zavros; Patrick H Maxwell; H Terence Cook; Panayiota Demosthenous; Andreas Hadjisavvas; Kyriacos Kyriacou; Ioanna Zouvani; Alkis Pierides; Constantinos Deltas
Journal:  Clin J Am Soc Nephrol       Date:  2011-05-12       Impact factor: 8.237

Review 3.  The role of molecular genetics in diagnosing familial hematuria(s).

Authors:  Constantinos Deltas; Alkis Pierides; Konstantinos Voskarides
Journal:  Pediatr Nephrol       Date:  2011-06-19       Impact factor: 3.714

  3 in total

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