What do you think? Once I asked one of my cardiologists, whether my little MVP is myxomatous. He answered, that the myxomatous tissue may well be seen on echocardiography and mine doesn't show these signs.
How do you thing about?
Ivo, let me complement you on your English. I, like you, had MVP when in my
20's I did well until my early 70's when I developed ruptured chordae tendinae and severe regurgitation. At surgery my surgeon found myxomatous degeneration so bad he couldn't do a repair, so he put in a St.Jude mechanical valve. It has served me well-10 years coming up in September.
Now, to answer your question, I think a small minority MVP will eventually proceed to regurgitation and myxomatous degeneration. As far as I know myxomatous degeneration can not be diagnosed by echo.Now that you have been diagnosed MVP I would advise an echo every year or so. A good cardiologist should listen to your heart for a change in heart sounds and/or signs of regurgitation.Don't let this diagnosis make you neurotic you very likely will never develop regurgitation or need surgery.