Evidence map›Paper›PMID 24475425›Full record

ArticleJournal of nephropathology2013

Histological patterns of idiopathic steroid resistant nephrotic syndrome in Egyptian children: A single centre study.

Elham Ibrahim Seif, Eman Abdel-Salam Ibrahim, Nadia Galal Elhefnawy, Manal Ibrahim Salman

Open access · goldAbstract read
In one paragraph

Article in Journal of nephropathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. MDR1 polymorphisms and idiopathic nephrotic syndrome in Slovak children: preliminary results.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Article
  7. Thrombotic microangiopathy in IgA nephropathy.Iranian Red Crescent medical journal · 2013
    Article
  8. Anti-phospholipase A2 receptor antibody in idiopathic membranous nephropathy: New concepts.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2013
    Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Elham Ibrahim SeifElectron microscopy unit and Pathology department. Ain Shams University Specialized Hospital (ASUSH),Faculty of Medicine-Ain Shams University, Cairo, Egypt.
Eman Abdel-Salam IbrahimElectron microscopy unit and Pathology department. Ain Shams University Specialized Hospital (ASUSH),Faculty of Medicine-Ain Shams University, Cairo, Egypt.
Nadia Galal ElhefnawyElectron microscopy unit and Pathology department. Ain Shams University Specialized Hospital (ASUSH),Faculty of Medicine-Ain Shams University, Cairo, Egypt.
Manal Ibrahim SalmanElectron microscopy unit and Pathology department. Ain Shams University Specialized Hospital (ASUSH),Faculty of Medicine-Ain Shams University, Cairo, Egypt.
Ain Shams University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

backgroundIdiopathic steroid resistant nephrotic syndrome (ISRNS) represents about 10-20% of children with nephrotic syndrome with variable outcome.

objectivesTo determine the histological patterns of ISRNS in Egyptian children and the histological details of the commonest types which might be the reason for the steroid resistance. PATIENTS AND

methodsThe study included 53 cases with ISRNS. Their renal biopsies were retrieved from the archive of Electron microscopy unit and pathology department, Ain Shams University Specialized Hospital (ASUSH) in the duration from 2005-2011. The biopsies were examined histologically, with immunohistochemistry, and by electron microscopy.

resultsThey were 36 males (67.9%) and 17 females (32.1%), the age at diagnosis ranged from 1.5- 16 years with a mean of 6.71 years. Lower limb oedema was the commonest presentation (100%), haematuria was revealed in (17%) of cases. Histological examination showed three major patterns; Focal segmental glomerulosclerosis (FSGS) in 30.2%, minimal change glomerulopathy (MCG) in 24.5% and IgA nephropathy in 13.2 %. Mesangial hypercellularity was very common among MCG patients (85.3% ±6.7). Tubulointerstitial inflammation and fibrosis were common among cases with IgA nephropathy (40.4% ±11, 53.7% ±8 respectively).

conclusionsISRNS in Egyptian children could be attributed mainly to three major diseases (FSGS, MCG and IgA nephropathy). Mesangial hypercellularity and severe tubulointerstitial disease might be the major causes for steroid resistance in MCG and IgA nephropathy respectively. Renal biopsy with electron microscopy examination should be done for all children with nephrotic syndrome at first time of presentation for proper assignment of treatment protocol.

Indexed as

Focal segmental glomerulosclerosis (FSGS)IgA nephropathyMesangial hypercellularityMinimal change glomerulopathy (MCG)Predinsone resistant nephrotic syndromeTubulointerstitial disease

Identifiers

PMID24475425
PMCPMC3886174
OpenAlexW2162308691

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.