Evidence map›Paper›PMID 39997047›Full record

ArticleDiseases (Basel, Switzerland)2025

A Retrospective Review of 28 Cases of Pediatric Malignant Renal Tumors at a Single Institution.

Takafumi Kawano, Koshiro Sugita, Ryuta Masuya, Nanako Nishida, Ayaka Nagano, Masakazu Murakami, Keisuke Yano, Shun Onishi, Toshio Harumatsu, Tatsuro Nakamura and 8 more

Abstract read
In one paragraph

Article in Diseases (Basel, Switzerland), 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

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

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

18 authors.

Takafumi KawanoDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0002-5920-453X
Koshiro SugitaDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Ryuta MasuyaDepartment of Gastrointestinal Surgery and Surgical Oncology, Ehime University Graduate School of Medicine, Matsuyama 791-0295, Japan.ORCID 0000-0002-5080-4846
Nanako NishidaDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Ayaka NaganoDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Masakazu MurakamiDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Keisuke YanoDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Shun OnishiDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0002-3984-3764
Toshio HarumatsuDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Tatsuro NakamuraDepartment of Pediatrics, Kagoshima University School of Medical and Dental Science, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0003-0214-8028
Koji YamadaDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Waka YamadaDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Mitsuru MutoDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.
Yuichi KodamaDepartment of Pediatrics, Kagoshima University School of Medical and Dental Science, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0003-1314-0371
Takuro NishikawaDepartment of Pediatrics, Kagoshima University School of Medical and Dental Science, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0001-5012-0906
Tatsuru KajiDepartment of Pediatric Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan.
Yasuhiro OkamotoDepartment of Pediatrics, Kagoshima University School of Medical and Dental Science, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0003-4412-6441
Satoshi IeiriDepartment of Pediatric Surgery, Research Field in Medical and Health Sciences, Medical and Dental Area, Research and Education Assembly, Kagoshima University, Kagoshima 890-8520, Japan.ORCID 0000-0002-1250-093X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in treatment have dramatically improved the outcomes of pediatric renal malignancies. We reviewed cases of renal malignant tumors that were managed in our institution. The patients' background factors, pathological diagnoses, stages, outcomes and late complications were retrospectively reviewed using medical records of 28 patients with renal tumors who were treated at our institution from 1984 to 2022. Wilms' tumors were recognized in 24 patients (85.7%), all of whom had favorable histology. Wilms' tumors were Stage I in six patients (6/24; 25.0%), Stage II in nine patients (9/24; 37.5%), Stage III in five patients (5/24; 20.8%), Stage IV in two patients (2/24; 8.3%), and Stage V in two patients (2/24; 8.3%). Two patients (7.1%) with clear cell sarcoma of the kidney both had Stage I disease. One patient had Stage IV rhabdoid sarcoma of the kidney (3.5%), and one had Stage IV renal cell carcinoma (3.5%). The overall 5-year survival rate was 85.2% for all renal malignancies. Late complications included chronic renal failure in four patients (14.2%). The outcomes are comparable to those reported previously. However, the prognosis of MRTK and renal cell carcinoma remained poor in advanced cases; thus, another therapeutic protocol should be established.

Indexed as

childrenmalignant rhabdoid tumorrenal cell carcinomaWilms’ tumor

Identifiers

PMID39997047
PMCPMC11854009

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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.