Evidence map›Paper›PMID 39981159›Full record

ArticleRadiology case reports2025

Partial anomalous pulmonary venous connection and an incidental aberrant right subclavian artery: A rare case report.

Ashish Khadka, Aakash Neupane, Pramodman Singh Yadav, Leeza Shah, Abinash Dev, Sabin Ghale, Amisha Karki

Abstract readCase Reports
In one paragraph

Article in Radiology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Ashish KhadkaDepartment of Radiodiagnosis and Imaging, National Academy of Medical Sciences, Kathmandu, Nepal.
Aakash NeupaneDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.
Pramodman Singh YadavDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.
Leeza ShahDepartment of Internal Medicine, Chitwan Medical College, Nepal.
Abinash DevDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.
Sabin GhaleDepartment of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.
Amisha KarkiDepartment of Internal Medicine, Bharatpur Hospital, Bharatpur, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital heart defect where some pulmonary veins drain into the right atrium instead of the left. We report a case of a 20-year-old female with worsening dyspnea and intermittent chest pain. Imaging revealed cardiomegaly and pulmonary hypertension on chest X-ray. Contrast-enhanced CT showed normal right pulmonary vein drainage but anomalous drainage of the left pulmonary veins into the left brachiocephalic vein. An incidental finding of an aberrant right subclavian artery (ARSA) was also noted. The patient underwent successful surgical correction of PAPVC, with no postoperative complications, though long-term follow-up was unavailable. PAPVC is often asymptomatic but can lead to right-sided heart failure and pulmonary hypertension if untreated. ARSA, a rare anomaly, was not clinically significant in this case. This report emphasizes the role of advanced imaging in diagnosing rare anomalies like PAPVC and ARSA, where early detection and intervention are crucial for preventing complications like right ventricular dysfunction and arrhythmias.

Indexed as

CardiologyComputed tomographyCongenital heart diseasesDyspneaPulmonary vein anomalies

Identifiers

PMID39981159
PMCPMC11840540

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