Evidence map›Paper›PMID 40416971›Full record

ArticleFrontiers in immunology2025

Clinicopathological features and genetic mutation spectrum of primary anastomosing hemangioma arising from the kidney.

Luxin Zhang, Haozhen Li, Heyao Tong, Hepeng Cui, Huahang Guo, Shuang Wen, Zhuwei Song, Jiaqiang Chen, Shengxiang Xiang, Zhiyu Liu and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. 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

12 authors.

Luxin Zhang *Department of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Haozhen Li *Department of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Heyao Tong *Department of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Hepeng CuiDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Huahang GuoDepartment of Pathology, Dalian Friendship Hospital, Dalian, Liaoning, China.
Shuang WenDepartment of Pathology, Dalian Friendship Hospital, Dalian, Liaoning, China.
Zhuwei SongDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Jiaqiang ChenDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Shengxiang XiangDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Zhiyu LiuDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Bo FanDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Liang WangDepartment of Urology, Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Renal anastomosing hemangioma (RAH) is a rare benign renal tumor, and its clinicopathologic characteristics and genetic mutation spectrum related to its mechanisms of pathogenesis are unclear. Methods: We carried out whole-genome sequencing (WGS) on RAH samples to explore the genetic mutation spectrum and verified the results by Sanger sequencing. Immunohistochemical analysis was also performed to reveal the histopathological characteristics and the tumor microenvironment components. Moreover, a population-based study was conducted after searching the PubMed, EMBASE, and Ovid SP databases to systematically summarize the clinicopathologic features of patients with RAH. Results: WGS analysis revealed 10532 somatic single-nucleotide variants (SNVs), 6705 somatic insertions and deletions (INDELs), and mutations in 32 predisposing genes and 10 driver genes, among which the mutations in 8 of the predisposing genes, Conclusions: The distinct phenotypes of RAH may be associated with the different genetic mutation spectra identified in our study. The presence or absence of comorbid ESRD varies among patients with RAH. However, additional studies are required to validate our results.

Indexed as

HemangiomaKidney NeoplasmsMutationAdultAgedBiomarkers, TumorFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedTumor MicroenvironmentWhole Genome SequencingBiomarkers, Tumorgene mutationsimmunoregulationpopulation-based studyrenal anastomosing hemangiomaswhole-genome sequencing

Identifiers

PMID40416971
PMCPMC12098607

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.