Document Detail


Alport-like glomerular changes in a patient with nephrotic syndrome: report of a case.
MedLine Citation:
PMID:  10975309     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report a 17-year-old Saudi girl who presented with nephrotic syndrome at the age of 7 years. A renal biopsy revealed a mildly proliferative immune complex-mediated glomerulonephritis, which on ultrastructural examination revealed prominent thickening of the capillary basement membranes, along with marked splitting and lamellation of lamina densa resembling those seen in Alport syndrome. These changes were even more pronounced in renal biopsies performed 1 and 3 years later, respectively. Thorough clinical evaluations and follow-up of more than 10 years failed to reveal any evidence of Alport syndrome. Review of the literature revealed four similar cases reported previously. Diffuse and prominent Alport-like glomerular changes may rarely be seen in patients with nephrotic syndrome in the absence of Alport syndrome. Pathogenesis of these changes, however, remains to be understood.
Authors:
M Akhtar; E Al-Sabban
Related Documents :
20110379 - Spontaneous remission of nephrotic syndrome in idiopathic membranous nephropathy.
19908069 - Membranous nephropathy in children: clinical presentation and therapeutic approach.
10872189 - Steroid-sensitive nephrotic syndrome associated with kimura disease.
662049 - Nephrotic syndrome and focal glomerular sclerosis in aging man.
19474279 - Congenital disorders of glycosylation: a rare cause of nephrotic syndrome.
17484229 - Spontaneous escherichia coli cellulitis in a child with nephrotic syndrome.
1143149 - Keratoconus and the ehlers-danlos syndrome: a new aspect of keratoconus.
4434089 - Haemoglobin belfast 15 (a12) tryptophan leading to arginine: a new unstable haemoglobin...
2628819 - Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: eem syndrome (...
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Pediatric nephrology (Berlin, Germany)     Volume:  14     ISSN:  0931-041X     ISO Abbreviation:  Pediatr. Nephrol.     Publication Date:  2000 Sep 
Date Detail:
Created Date:  2000-12-04     Completed Date:  2000-12-14     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8708728     Medline TA:  Pediatr Nephrol     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  973-5     Citation Subset:  IM    
Affiliation:
Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. akhtar@kfshrc.edu.sa
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Basement Membrane / ultrastructure
Capillaries / pathology
Female
Humans
Kidney Glomerulus / blood supply,  pathology*
Nephritis, Hereditary / pathology*
Nephrotic Syndrome / pathology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases.
Next Document:  C1q nephropathy presenting as rapidly progressive crescentic glomerulonephritis.