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Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2013 / Cilt: 21 - Sayı: 3

Anomalous origin of the left coronary artery from the pulmonary artery in an adult patient presenting with congestive heart failure

Konjesif kalp yetersizliğinin eşlik ettiği erişkin bir hastada pulmoner arterden kaynaklanan anomalili sol koroner arter

Cem ARITÜRK
Mustafa ÇETİN
Orhan KARABÖRK
Ekrem AKSU
Cem ATİK
Pages
786–788
Publication Date
2022-09-02
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this article, we report a 36-year-old female patient who was diagnosed with ALCAPA when we investigated the reason for the left ventricular dysfunction.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a very rare congenital defect associated with myocardial ischemia, congestive heart failure and death in the early period of life.
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Key Findings & Data:Therefore, it is uncommon for an ALCAPA patient to survive to adulthood.
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Conclusion & Impact:In this article, we report a 36-year-old female patient who was diagnosed with ALCAPA when we investigated the reason for the left ventricular dysfunction.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a very rare congenital defect associated with myocardial ischemia, congestive heart failure and death in the early period of life. Therefore, it is uncommon for an ALCAPA patient to survive to adulthood. In this article, we report a 36-year-old female patient who was diagnosed with ALCAPA when we investigated the reason for the left ventricular dysfunction.

Özet

Pulmoner arterden kaynaklanan anomalili sol koroner arter(ALCAPA), yaşamın erken döneminde miyokardiyal iskemi, konjesif kalp yetersizliği ve ölümle ilişkili çok nadir görülen bir doğumsal defekttir. Bu nedenle bir ALCAPA hastasının erişkin yaşa kadar hayatta kalması ender görülen bir durumdur. Bu yazıda sol ventriküler disfonksiyonun nedeni araştırılırken ALCAPA tanısı konulan 36 yaşında bir kadın olgu sunuldu.

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Cite This Article

ARITÜRK, C., ÇETİN, M., KARABÖRK, O., AKSU, E., ATİK, C. (2022). Anomalous origin of the left coronary artery from the pulmonary artery in an adult patient presenting with congestive heart failure. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 21 - Sayı: 3, 786–788. https://ajindex.com/articles/424593

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References (1)

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