Evidence map›Paper›PMID 40322125›Full record

ArticleTurk gogus kalp damar cerrahisi dergisi2024

[MEP-32] Unusual Origin of Anomalous Left Main Coronary Artery From the Pulmonary Artery.

Arda Sezen, Defne Gunes Ergi, Akin Cinkooglu, Eser Dogan, Mahsati Akhundova, Osman Nuri Tuncer, Yuksel Atay

Abstract read
In one paragraph

Article in Turk gogus kalp damar cerrahisi dergisi, 2024. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Arda SezenDepartment of Cardiovascular Surgery, Ege University Faculty of Medicine, İzmir, Türkiye.
Defne Gunes ErgiDepartment of Cardiovascular Surgery, Ege University Faculty of Medicine, İzmir, Türkiye.
Akin CinkoogluDepartment of Radiology, Ege University Faculty of Medicine, İzmir, Türkiye.
Eser DoganDepartment of Pediatric Cardiology, Ege University Faculty of Medicine, İzmir, Türkiye.
Mahsati AkhundovaDepartment of Cardiovascular Surgery, Ege University Faculty of Medicine, İzmir, Türkiye.
Osman Nuri TuncerDepartment of Cardiovascular Surgery, Ege University Faculty of Medicine, İzmir, Türkiye.
Yuksel AtayDepartment of Cardiovascular Surgery, Ege University Faculty of Medicine, İzmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we presented a case of an anomaly in which the left main coronary artery (LMCA) originates from the right pulmonary artery (RPA). A six-year-old female patient presented for a cardiology follow-up due to the mother's history of sudden cardiac death. On transthoracic echocardiography, the right coronary artery (RCA) was dilated, and the LMCA was not identified. There was no LMCA ostium on the aorta. The computed tomography and the coronary angiography revealed the wide and tortuous RCA originating from the aorta. Following primary median sternotomy, proximal visualization of the coronary ostium was challenging. Cardioplegia was given via the aortic root, revealing leakage from the RPA. For better visualization of the RPA, the aorta was transected above the RCA ostium. Subsequently, the MPA incision was extended towards the RPA, facilitating the coronary ostium visualization. Afterward, the left coronary ostium was freed from the RPA and implanted at its anatomical location on the ascending aorta. Subsequently, the RPA and MPA incisions were reconstructed with 7-0 Prolene sutures. The aortotomy was closed with a bovine patch, and warming was recommenced. The postoperative course was uneventful, and the patient was discharged on the seventh postoperative day. Complex cases of anomalous left main coronary artery from the pulmonary artery are surgically challenging. In rare instances where the LMCA originates from the RPA, ostial identification can be difficult. Detailed imaging is crucial for surgical planning. Conventional translocation is the gold standard method for these cases. This rare anomaly, also scarcely reported in the literature, is a variation that should be carefully considered in congenital heart surgery and coronary artery disease diagnosis.

Indexed as

Anomalous left main coronary artery from the pulmonary arteryBland-White-Garland syndromeleft main coronary arteryright pulmonary artery.

Identifiers

PMID40322125
PMCPMC12045217

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