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Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2004 / Cilt: 12 - Sayı: 3

Orthotopic cardiac transplantation in a patient with familial restrictive cardiomyopathy: Case report

Ailevi restriktif kardiyomiyopatili hastada ortotopik kalp transplantasyonu: Olgu sunumu

Mete ALP
Deniz GÖKSEDEF
Cevat YAKUT
Ercan EREN
Mustafa GÜLER
Suat Nail ÖMEROĞLU
Pages
188–190
Publication Date
2022-09-02
DOI
—
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AI Summary & Key Takeaways

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

Its diagnosis, follow-up, familial screening, and its treatment by a successful orthotopic heart transplantation with literature reviews are presented.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Restrictive cardiomyopathy is a rare disease which has a poor prognosis if it is left untreated.
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Key Findings & Data:We herein report a case with familial restrictive cardiomyopathy which has been the only one case in our heart transplantation series with 27 cases since 1989.
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Conclusion & Impact:Its diagnosis, follow-up, familial screening, and its treatment by a successful orthotopic heart transplantation with literature reviews are presented.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Restrictive cardiomyopathy is a rare disease which has a poor prognosis if it is left untreated. Etiologically, it may result from secondary to some storage diseases and/or primary (idiopathic) or familial. The definitive treatment is heart transplantation. We herein report a case with familial restrictive cardiomyopathy which has been the only one case in our heart transplantation series with 27 cases since 1989. Its diagnosis, follow-up, familial screening, and its treatment by a successful orthotopic heart transplantation with literature reviews are presented.

Özet

Restriktif kardiyomiyopati, nadir görülen ve tedavi edilmediği zaman prognozu kötü seyreden bir kardiyomiyopati türüdür. Etiyolojik olarak bazı depo hastalıklarına bağlı sekonder olabileceği gibi primer (idyopatik) veya ailesel karakterde de olabilir. Bu hastalığın kesin tedavisi kalp transplantasyonudur. Kliniğimizdeki 1989 yılından bugüne kadar yapılan 27 kalp transplantasyonları arasında tek ailesel restriktif kardiyomiyopatili olgunun tanısı, takibi, aile taraması ve ortotopik kalp transplantasyonu ile sonuçlanan başarılı tedavisi ve literatür incelemesi sunulmuştur.

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Cite This Article

ALP, M., GÖKSEDEF, D., YAKUT, C., EREN, E., GÜLER, M., ÖMEROĞLU, S. N. (2022). Orthotopic cardiac transplantation in a patient with familial restrictive cardiomyopathy: Case report. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 12 - Sayı: 3, 188–190. https://ajindex.com/articles/425340

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References (8)

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