Journals / Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi / 2018 / Cilt: 32 - Sayı: 2

A CASE OF RESTRICTIVE CARDIOMYOPATHY IN CHILDHOOD PRESENTING WITH WEAKNESS AND ANOREXIA

Halsizlik ve iştahsızlık yakınması ile gelen restriktif kardiyomiyopatili bir olgu

Pages
151–155
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

In this article a patient at 2.5 years of age with RCM is discussed regarding the literature.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Restrictive cardiyomyopathy (RCM) is a very rarely diagnosed cardiyomyopathy in childhood.
📊
Key Findings & Data:Biatrial enlargement and normal sized ventricles with normal or increased ventricular wall thickness are the characteristic morphological features of RCM.
💡
Conclusion & Impact:In this article a patient at 2.5 years of age with RCM is discussed regarding the literature.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Restriktif kardiyomiyopati · Konstriktif perikardit · çocuk

Abstract

Restrictive cardiyomyopathy (RCM) is a very rarely diagnosed cardiyomyopathy in childhood. Most RCM in childhood is idiopathic with a high mortality. Biatrial enlargement and normal sized ventricles with normal or increased ventricular wall thickness are the characteristic morphological features of RCM. The differential diagnosis of constrictive pericarditis is important. In this article a patient at 2.5 years of age with RCM is discussed regarding the literature.

Özet

Restriktif kardiyomiyopati (RKMP) çocukluk çağının nadir görülen kardiyomiyopatilerindendir. Çocukluk çağı RKMP’lerinin çoğunda altta yatan patoloji bulunamaz ve mortalitesi yüksektir. Karakteristik morfolojik özelliği ventrikül boyutları normal, ventriküler duvar kalınlığı normal veya artmış ve biatriyal büyümedir. Konstriktif perikarditle ayırıcı tanısı önem taşır. Bu yazıda, 2,5 yaşında RKMP’li bir olgu literatür eşliğinde tartışılmıştır.

🔖

Cite This Article

DEMİRCAN, T., KIZILCA, Ö., ZİHNİ, C., ÖNCÜ, B., KIR, M., ÜNAL, N. (2018). A CASE OF RESTRICTIVE CARDIOMYOPATHY IN CHILDHOOD PRESENTING WITH WEAKNESS AND ANOREXIA. Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi, Cilt: 32 - Sayı: 2, 151–155. https://ajindex.com/articles/152549

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (8)

  1. Report of the WHO/ISFC Task Force on the Definition and Classificatio of Cardiomyopathies. Br Heart J. 1980;44:672– 673. Maron BJ, Towbin JA, Thiene G, Antzelevitch C, Corrado D, Contemporary Definitions and Classification of the Cardiomyopathies: An American Heart Association Scientific Statement From the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation 2006;113:1807-1816
  2. Rachel J. Weller, Robert Weintraub, Linda J. Addonizio et all. Outcome of Idiopathic Restrictive Cardiomyopathy in Children. Am J Cardiol 2002;90:501–506
  3. Ammash N. M., Seward J. B., Bailey K. R., Edwards W. D., Tajik A. J. Clinical profile and outcome of idiopathic restrictive cardiomyopathy. Circulation. 2000;101(21):2490–2496. doi: 10.1161/01.CIR.101.21.2490. Denfield SW. Restrictive Cardiomypathy In:Allen H.D.,Driscoll D.J.,Shaddy R.E.,Feltes T. Moss and Adams' heart disease in infants, children, and adolescents: including the fetus and young adult. 8 th ed. Philadelphia: Lippincott Williams & Wilkins; 2013 p.1267-1276
  4. Çil E., Özkutlu S, Saraçlar M. Ve ark. Çocuklarda restriktif kardiyomiyopati: 12 va¬kanın klinikopatolojik incelemesi. Türk Kardiol Der Arş 1995;23:123-7.
  5. Walsh M.A., Grenier M.A. et all. Conduction abnormalities in pediatric patients with restrictive cardiomyopathy. Circ Heart Fail. 2012;5:267-73.
  6. Özkutlu S, Karagöz T. Restriktif kardiyomiyopati. Katkı Pediatri Dergisi 2001;22:51-63
  7. Zwas DR, Gotsman I, Admon D, Keren A. Advances in the differentiation of constrictive pericarditis and restrictive cardiomyopathy. Herz 2012;37:664-74. Sorajja P. Invasive hemodynamics of constrictive pericarditis, restrictive cardiomyopathy, and cardiac tamponade. Cardiology Clinics. 2011;29:191–199. doi: 10.1016/j.ccl.2011.01.003. L M Russo and S A Webber Idiopathic restrictive cardiomyopathy in children Heart. 2005; 91: 1199–1202.
  8. Elliott P., Andersson B., Arbustini E., et al. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases. Eur Heart J. 2008;29(2):270–276. doi: 10.1093/eurheartj/ehm342. Cooper L. T., Baughman K. L., Feldman A. M., et al. The role of endomyocardial biopsy in the management of cardiovascular disease: a scientific statement from the American Heart Association, the A