Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2005 / Cilt: 13 - Sayı: 4

Homozigot ailesel hiperkolesterolemili bir hastada cerrahi tedavi

Surgical collection in a patient with homozygous familial hypercholesterolemia

Pages
366–368
Publication Date
2022-09-02
DOI
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AI Summary & Key Takeaways

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

The postoperative course was uneventful and no recurence was observed within a follow-up of two years.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Familial hypercholesterolemia is characterized by rapidly progressing coronary atherosclerosis and aortic stenosis.
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Key Findings & Data:A 21-year-old man presented with anginal pain.
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Conclusion & Impact:The postoperative course was uneventful and no recurence was observed within a follow-up of two years.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Familial hypercholesterolemia is characterized by rapidly progressing coronary atherosclerosis and aortic stenosis. A 21-year-old man presented with anginal pain. He was diagnosed as having homozygous familial hypercholesterolemia and treated with coronary artery bypass grafting, aortic root enlargement, and aortic valve replacement. The postoperative course was uneventful and no recurence was observed within a follow-up of two years.

Özet

Ailesel hiperkolesterolemi koroner arterlerde hızlı gelişen ateroskleroz ve aort stenozu ile karakterize bir hastalıktır. Göğüs ağrısı şikayetiyle başvuran 21 yaşındaki bir erkek hasta, homozigot ailesel hiperkolesterolemi tanısıyla aortokoroner bypass, aortik kök genişletme ve aort kapak replasmanı ile tedavi edildi. Ameliyat sonrası dönemi sorunsuz geçen hastanın iki yıllık takibi süresince nüks saptanmadı.

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Cite This Article

POÇAN, S., SANİOĞLU, S., YILMAZ, A. T., SÜNGÜN, M., US, M. H. (2022). Homozigot ailesel hiperkolesterolemili bir hastada cerrahi tedavi. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 13 - Sayı: 4, 366–368. https://ajindex.com/articles/425306

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References (6)

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