eISSN: 2300-6722
ISSN: 1899-1874
Medical Studies/Studia Medyczne
Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
Editorial System
Submit your Manuscript
4/2019
vol. 35
 
Share:
Share:
abstract:
Case report

History and management of congenital aortic stenosis and coarctation of the aorta in a 38-year-old patient

Izabela Wojarska
1
,
Jadwiga Bednarek
1
,
Ewelina Nowak
1, 2
,
Anna Polewczyk
1, 3

1.
Collegium Medicum, Jan Kochanowski University, Kielce, Poland
2.
Department of Anesthesiology and Intensive Care Unit No. 2, Swiętokrzyskie Cardiology Centre, Kielce, Poland
3.
Swietokrzyskie Cardiology Centre, Kielce, Poland
Medical Studies/Studia Medyczne 2019; 35 (4): 324–326
Online publish date: 2019/12/30
View full text Get citation
 
PlumX metrics:
We present the case of a 38-year-old woman with congenital aortic stenosis as well as coarctation of the aorta that was unrecognised in her childhood. The patient was treated by balloon valvuloplasty. Ten years after the procedure, clinical deterioration was observed with subsequent progression of valvular gradient, aortic regurgitation, and diagnosis of coarctation. At the age of 38 years, a routine echocardiographic test showed massive calcifications of aortic leaflets with a transvalvular gradient 77/41 mm Hg, and third-degree insufficiency with widening of the ascending aorta (42 mm) and normal left ventricle systolic function. Additionally, for the first time the test showed coarctation of the aorta – narrowing in the isthmus below the arch down to 15 mm, with a maximum flow gradient ca. 60 mm Hg. The management of the complex heart defects is currently being considered.
keywords:

congenital aortic stenosis, coarctation of aorta, balloon valvuloplasty, hybrid therapy

Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.