Evidence map›Paper›PMID 36405826›Full record

ArticleFrontiers in pediatrics2022

Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur.

Tong Qiu, Yuru Lan, Jiangyuan Zhou, Kaiying Yang, Xue Gong, Zixin Zhang, Siyuan Chen, Yi Ji

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Primary osseous kaposiform hemangioendothelioma confined to long bones: a retrospective imaging analysis of 12 pediatric cases.Cancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Article
  2. Article
  3. A case report of primary Kaposiform hemangioendothelioma of the humerus.International journal of immunopathology and pharmacology
    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

8 authors at 2 institutions in 1 country.

Tong QiuDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Yuru LanDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Jiangyuan ZhouDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Kaiying YangDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Xue GongDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Zixin ZhangDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Siyuan ChenPediatric Intensive Care Unit, Department of Critical Care Medicine, West China Hospital of Sichuan University, Chengdu, China.
Yi JiDivision of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China.
Sichuan University · CNWest China Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kaposiform hemangioendothelioma (KHE) is a rare borderline vascular tumor that usually presents as a mass of skin or deep soft tissue. We report a unique case of an 8-year-old KHE patient with bilateral symmetrical sites involving both femurs. The laboratory, radiographic, and pathological findings of the patient were minutely described. During the 6-month follow-up, the symptoms of pain and dysfunction of this patient were relieved. This study aimed to arouse clinicians' concern about the symmetrical sites of KHE patients.

Indexed as

bonecase reportkaposiform hemangioendotheliomaKasabach–Merritt phenomenonpediatric

Identifiers

PMID36405826
PMCPMC9672085
OpenAlexW4308202359

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.