Evidence map›Paper›PMID 42237331›Full record

ArticleJournal of cardiothoracic surgery2026

Pulmonary valve and supravalvular membrane fusion: a case report.

Xia Chen, Aoli Huang, Xujing Zhu, Renyuan Li

Abstract readCase Reports
In one paragraph

Article in Journal of cardiothoracic surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xia ChenDepartment of Nursing, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Aoli HuangDepartment of Nursing, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xujing ZhuDepartment of Nursing, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Renyuan LiDepartment of Cardiovascular Surgery, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China. renyuanzyyy@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIsolated congenital supravalvular pulmonary stenosis is an exceedingly rare cardiac anomaly, typically characterized by a discrete membrane above the valve obstructing the main pulmonary artery. We present a previously unreported anatomical variation in which this membrane fused with one of the pulmonary valve leaflets, forming a distinct pouch-like configuration. CASE PRESENTATION: A 44-year-old male presented with progressive exertional dyspnea. Preoperative echocardiography identified severe pulmonary stenosis and an obstructing supravalvular membrane, with a peak transvalvular gradient of 170 mmHg. Intraoperative exploration revealed that the pulmonary valve is trileaflet, with visibly thickened and fused commissures, causing severe pulmonary valve stenosis. Uniquely, the supravalvular pulmonary membrane fused with one leaflet forming a pouch-like configuration. Surgical separation of the fused commissures was performed, which successfully relieved the obstruction. The patient recovered well and reported complete symptom resolution at one-month follow-up.

conclusionThis case presents a unique anatomical variant of isolated congenital supravalvular pulmonary stenosis, characterized by fusion between the abnormal supravalvular membrane and one valve leaflet. The surgical approach adopted achieved acceptable results and substantially improved the patient's clinical condition.

Indexed as

Pulmonary ValvePulmonary Valve StenosisAdultEchocardiographyHumansMaleCommissure fusionSupravalvular membraneSupravalvular pulmonary stenosis

Identifiers

PMID42237331
PMCPMC13455304

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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.