Site icon All About Cardiovascular System and Disorders

Bilateral conus and Absent conus

YouTube video player

Bilateral conus and Absent conus

Bilateral conus is seen in double outlet right ventricle. Conus is manifest as a semilunar valve – AV valve discontinuity with the conus tissue in between. In normal heart conus is seen below the pulmonic valve, but not below the aortic valve, so that there is mitral-aortic continuity and tricuspid-pulmonary discontinuity.

Bilateral conus is also present in Taussig Bing anomaly which is a variant of double outlet right ventricle [1]. Both conal free walls are muscular and well developed. The muscular conal free walls prevent atrioventricular valve semilunar valve fibrous continuity. About 9 mm of conal tissue separate the pulmonary valve from the mitral valve. There is transposition of great arteries in Taussig Bing Anomaly. Tricuspid valve is separated from the aortic valve by a conal muscular tissue of about 8 mm.

In general it is often mentioned that absent conus is seen in dextro transposition of great arteries. But a study which reported conal anatomy in 119 patients with D-loop transposition of great arteries and ventricular septal defect reported different findings [2]. 88.2% had subaortic conus with no subpulmonary conus. Subarterial conus was seen bilaterally in 6.7% cases. 3.4% had only subpulmonary conus with minimal or no subaortic conus. Subarterial conus was bilaterally absent in only 1.7%. This variability in conal anatomy in D-TGA with VSD implies four different mechanisms by which transposition occurs.

References

  1. Van Praagh R. What Is the Taussig-Bing Malformation? Circulation. 1968 Sep;38(3):445-9.
  2. L Pasquini, S P Sanders, I A Parness, S D Colan, S Van Praagh, J E Mayer Jr, R Van Praagh. L Pasquini, S P Sanders, I A Parness, S D Colan, S Van Praagh, J E Mayer Jr, R Van Praagh. Conal Anatomy in 119 Patients With D-Loop Transposition of the Great Arteries and Ventricular Septal Defect: An Echocardiographic and Pathologic Study.
    J Am Coll Cardiol. 1993 Jun;21(7):1712-21.
Exit mobile version