Evidence map›Paper›PMID 41948059›Full record

ArticleCase reports in nephrology2026

Nephrotic-Nephritic Syndrome Following Unilateral Nephrectomy in Wilms Tumour in a Child.

Rawshan Zuhair Jaber

Abstract read
In one paragraph

Article in Case reports in nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

1 citing paper in PubMed.

  1. 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

1 author.

Rawshan Zuhair JaberDepartment of Oncology, Basrah Specialty Teaching Hospital for Children, Basrah Health Directorate, Basrah, Iraq.ORCID https://orcid.org/0000-0002-9878-5250

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Wilms tumour (WT) represents the most frequent kidney malignant tumour in the paediatric population and is occasionally linked to specific congenital syndromes. Treatment typically includes multimodal therapy consisting of chemotherapy, surgery and/or radiotherapy (RT), with a success rate of approximately 90%. The incidence of nephrotic-nephritic syndrome following unilateral nephrectomy is extremely rare; however, certain long-term kidney complications have been documented. Case Report: A 5-year-old female was diagnosed with WT, Stage 3 with favourable histology. She underwent left radical nephrectomy with preoperative spillage and received RT for the whole abdomen followed by chemotherapy. She was complaint from insidious onset fever, shortness of breath, progressive generalized oedema, reddish urine and headache, occurring 5 days from the 5 Conclusion: Kidney injury poses a risk in cases following nephrectomy, with hyperfiltration, treatment toxicity and immune effects contributing to the condition. Early detection and management are essential for kidney preservation.

Indexed as

nephrectomynephrotic–nephritic syndromeWilms tumour

Identifiers

PMID41948059
PMCPMC13051904

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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.