Evidence map›Paper›PMID 37029383›Full record

ArticleJournal of cardiothoracic surgery2023

Cardiac endothelial sarcoma with hypereosinophilia of children: a case report.

Wei Zhang, Mengyuan He, Qiang Wang

Abstract readCase Reports
In one paragraph

Article in Journal of cardiothoracic surgery, 2023. 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

3 authors.

Wei Zhang *Department of Cardiac Surgery, Tianjin Chest Hospital, Tianjin, China.
Mengyuan He *Tianjin Medical University, Tianjin, China.
Qiang WangDepartment of Cardiac Surgery, Tianjin Chest Hospital, Tianjin, China. 15622197121@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac malignancies in children are extremely rare and they with hypereosinophilia are rather relatively uncommon. The majority of individuals may survive over the long term even with heart tumors provided they don't have any significant symptoms and their hemodynamics are unaffected. But we should nevertheless be aware of them, especially when they are coupled with persistent hypereosinophilia and the development of a hemodynamic anomaly. The case of a malignant heart tumor with hypereosinophilia in a 13-year-old girl is presented in this paper. She exhibited an echocardiographic deficit and a heart murmur. Additionally, it was difficult to treat her hypereosinophilia. Nevertheless, it was resolved the day after the operation. We presume that there is a certain relationship between them. This study gives clinicians a wide range of options for analyzing the connections between malignancy and hypereosinophilia.

Indexed as

EosinophiliaHeart NeoplasmsMediastinal NeoplasmsSarcomaSoft Tissue NeoplasmsThymus NeoplasmsAdolescentChildFemaleHumansCardiac tumorChildrenEosinophiliaHypereosinophiliaMalignancy

Identifiers

PMID37029383
PMCPMC10080960

What OpenQuestion holds

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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 OpenQuestion graph.