Journals / Medeniyet Medical Journal / 2017 / Cilt: 32 - Sayı: 3

A rarely seen congenital malformation in an elderly patient: Uhl’s anomaly

Yaşlı bir hastada nadir bir konjenital malformasyon: Uhl’s anomalisi

Pages
202–204
Publication Date
2022-11-05
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)

Here, we report a rare case of UA which had been misdiagnosed as Ebstein’s anomaly in a 62-year-old female.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Uhl’s anomaly (UA) is a rare congenital malformation described as the partial or complete absence of the myocardium of the right ventricle.
📊
Key Findings & Data:UA is commonly confused with arrhythmogenic right ventricular dysplasia or Ebstein’s anomaly.
💡
Conclusion & Impact:Here, we report a rare case of UA which had been misdiagnosed as Ebstein’s anomaly in a 62-year-old female.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Uhl’s anomaly (UA) is a rare congenital malformation described as the partial or complete absence of the myocardium of the right ventricle. UA is commonly confused with arrhythmogenic right ventricular dysplasia or Ebstein’s anomaly. Cardiac magne- tic resonance imaging (MRI) is the gold standard diagnostic tech- nique for the differential diagnosis of UA. Here, we report a rare case of UA which had been misdiagnosed as Ebstein’s anomaly in a 62-year-old female.

Özet

Uhl’s Anomalisi (UA) sağ ventrikülde parsiyel ya da total miyo- kard yokluğu ile tanımlanan nadir bir konjenital malformasyon- dur. UA sıklıkla aritmojenik sağ ventrikül displazisi veya Ebstein’s anomalisi ile karıştırılır. UA’nın ayırıcı tanısında kardiyak magne- tik rezonans görüntüleme, altın standart tanı tekniğidir. Burada nadir olarak 62 yaşında Ebstein’s anomalisi yanlış tanısı almış bir UA olgusunu sunacağız.

🔖

Cite This Article

KUL, Ş., KELEŞ, N., ÖZKÖK, S., DEMİRCİOGLU, K., ÇALIŞKAN, M. (2022). A rarely seen congenital malformation in an elderly patient: Uhl’s anomaly. Medeniyet Medical Journal, Cilt: 32 - Sayı: 3, 202–204. https://ajindex.com/articles/343420

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (4)

  1. Epstein ML. Congenital stenosis and insufficiency of tricus- pid valve. Uhl’s anomaly. Moss and Adams Hearts Disease of Infant, Children and Adolescents. 6th ed. Lippincott Willams and Wilkins, Phildelphia; 2000. p. 816-8. Perloff JK, editor. Uhl’s anomaly. In: The Clinical Recognition of Congenital Heart Disease. 5th ed. Philadelphia: Saunders; 2003. p. 209-15.
  2. Goksin I, Baltalarlı A, Evrengul M, et al. Ebstein’s anomaly in a 16-year-old child presenting with cyanosis and syncope. Turk Gogus Kalp Dama 2008;16:183-5.
  3. Ganczar J, English R. Uhl’s anomaly: Absence of the right ventricular myocardium. Ann Pediatr Cardiol 2015;8:71-3. https://doi.org/10.4103/0974-2069.149529 Song BG. A rare case of partial absence of the right ventri- cular musculature in asymptomatic adult man: partial Uhl’s anomaly. Heart Lung 2013;42:215-7. https://doi.org/10.1016/j.hrtlng.2013.02.001
  4. Güler N, Demirbag R, Eryonucu B, Gül A. A case of successful six consecutive deliveries in a 41-year-old woman with Uhl’s anomaly. Int J Cardiol 2003;87:283-5. https://doi.org/10.1016/S0167-5273(02)00306-6