Literature DB >> 16362391

Thin basement membrane nephropathy associated with minimal change disease in a 15-year-old boy.

Shuichiro Fujinaga1, Kazunari Kaneko, Yoshiyuki Ohtomo, Hitohiko Murakami, Mayako Takemoto, Masaru Takada, Toshiaki Shimizu, Yuichiro Yamashiro.   

Abstract

Thin basement membrane nephropathy (TBMN) is characterized clinically by persistent hematuria, minimal proteinuria, normal renal function, another family member with hematuria, and a benign course. Especially in childhood TBMN, proteinuria of any degree is reported to be uncommon. We report on a boy with benign familial hematuria found by urinary screening at 3 years of age who presented with nephrotic syndrome (NS) at 15 years of age. His renal histology showed TBMN associated with minimal change disease (MCD). Treatment with corticosteroid resulted in complete remission of NS in a short period of time, while isolated hematuria persisted during the follow-up period despite this therapy. We speculate, therefore, that the nephrotic range proteinuria is not due to TBMN but rather is the manifestation of associated MCD. Several cases of TBMN with NS have been reported in adults, but it has not yet been reported in children in the literature. To our knowledge, this is the first case of childhood TBMN associated with NS resulting from coincidental MCD.

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Year:  2005        PMID: 16362391     DOI: 10.1007/s00467-005-2095-2

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  12 in total

1.  Thin basement membrane disease with heavy proteinuria or nephrotic syndrome at presentation.

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Journal:  Am J Kidney Dis       Date:  2000-04       Impact factor: 8.860

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3.  Establishment by the rat lymph node method of epitope-defined monoclonal antibodies recognizing the six different alpha chains of human type IV collagen.

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Journal:  Histochem Cell Biol       Date:  1995-10       Impact factor: 4.304

Review 4.  Thin basement membrane nephropathy associated with other glomerular diseases.

Authors:  Suzanne M Norby; Fernando G Cosio
Journal:  Semin Nephrol       Date:  2005-05       Impact factor: 5.299

Review 5.  The risks of thin basement membrane nephropathy.

Authors:  Stephen Tonna; Yan Yan Wang; Duncan MacGregor; Roger Sinclair; Paul Martinello; David Power; Judy Savige
Journal:  Semin Nephrol       Date:  2005-05       Impact factor: 5.299

6.  Signs and symptoms of thin basement membrane nephropathy: a prospective regional study on primary glomerular disease-The Limburg Renal Registry.

Authors:  Pieter van Paassen; Peter J C van Breda Vriesman; Henk van Rie; Jan Willem Cohen Tervaert
Journal:  Kidney Int       Date:  2004-09       Impact factor: 10.612

7.  Thin-glomerular-basement-membrane nephropathy: is it a benign cause of isolated hematuria?

Authors:  Saumil Gandhi; Kamyar Kalantar-Zadeh; Burl R Don
Journal:  South Med J       Date:  2002-07       Impact factor: 0.954

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Journal:  J Pathol       Date:  1984-04       Impact factor: 7.996

9.  Glomerular basement membrane and lamina densa in infants and children: an ultrastructural evaluation.

Authors:  C Vogler; A J McAdams; S M Homan
Journal:  Pediatr Pathol       Date:  1987

10.  The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children.

Authors: 
Journal:  J Pediatr       Date:  1981-04       Impact factor: 4.406

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  4 in total

1.  Novel heterozygous COL4A3 mutation in a family with late-onset ESRD.

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Journal:  Pediatr Nephrol       Date:  2010-02-23       Impact factor: 3.714

2.  Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.

Authors:  Stefanie Weber; Katja Strasser; Sabine Rath; Achim Kittke; Sonja Beicht; Martin Alberer; Bärbel Lange-Sperandio; Peter F Hoyer; Marcus R Benz; Sabine Ponsel; Lutz T Weber; Hanns-Georg Klein; Julia Hoefele
Journal:  Pediatr Nephrol       Date:  2016-01-25       Impact factor: 3.714

3.  Phenotype variability in a large Spanish family with Alport syndrome associated with novel mutations in COL4A3 gene.

Authors:  C Cervera-Acedo; A Coloma; E Huarte-Loza; M Sierra-Carpio; E Domínguez-Garrido
Journal:  BMC Nephrol       Date:  2017-10-31       Impact factor: 2.388

4.  Minimal change disease with concurrent thin basement membrane disease: A case report.

Authors:  Abdulaziz I Alroshodi
Journal:  Int J Health Sci (Qassim)       Date:  2020 May-Jun
  4 in total

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