Evidence map›Paper›PMID 40129537›Full record

ArticleUrology case reports2025

Recurrent extrarenal Teratoid Wilms tumor in sacrococcygeal region of children after initial surgery: A rare case.

Xian Wei, Ting Li, Xiaojuan Wu

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Urology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Xian WeiDepartment of Pediatric Surgery Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Ting LiDepartment of Pediatric Surgery Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Xiaojuan WuDepartment of Pediatric Surgery Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Teratoid Wilms tumor is a very rare tumor, about 70 cases have been reported worldwide. Extrarenal teratoid Wilms tumor is even less common. We reported a child with sacrococcygeal teratoid Wilms tumor who was diagnosed with teratoma at the time of the initial operation and relapsed shortly after the operation; we followed up for nearly two years after the second operation with no tumor recurrence or metastasis. This case tells clinicians that the diagnosis of extrarenal teratoid Wilms tumor needs to be careful, and although the prognosis of the disease is good, the premise is complete surgical resection.

Indexed as

Case reportRare diseaseRecurrenceTeratoid Wilms tumor

Identifiers

PMID40129537
PMCPMC11930740

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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.