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Case from: Eliza Panczyk, Andrea Tackett, Sachin Kumar, Vincent L. Sorrell, Department of Cardiology, University of Arizona, Tucson AZ, USA
History: 35 year old man. Known congenital bicuspid aortic
valve. Recently noted ascending aortic dilatation on routine echocardiogram.
Referred for a cardiac MRI for LV functional and morphologic assessment and
contrast MRA for aortic evaluation.
CMR: The ascending aorta was dilated - maximal diameter
50 mm (top). The aortic valve was bicuspid and non-stenotic (short axis cine).
One leaflet is larger, containing a shallow ridge or raphe – the site
of the congenital fusion of the original commissures (occurs in 60% of cases).
There is moderate AR. Mildly dilated LV cavity with AR jet coursing along the
anterior leaflet of the mitral valve (LVOT cine). No coarctation was present.
Discussion: The aorta of patients with congenital bicuspid
aortic valve has intrinsic pathoanatomic changes detectable on histopathology
which make such individuals predisposed to progressive aortic aneurysmal dilatation
and aortic dissection. This can occur even in absence of hemodynamically significant
aortic stenosis or regurgitation. For this reason, repair or replacement of
aortic root and the ascending aorta is indicated during concurrent aortic valve
replacement if the diameter is greater than 45 mm or independently if the aortic
root and ascending aorta diameter is greater than 50 mm or the rate of increase
is 5 mm per year.(1,2)
References:
1. Della Corte A, et al:Predictors of ascending aortic dilatation
with bicuspid aortic valve: a wide spectrum of disease expression. Eur
J Cardiothorac Surg. 2007 Mar;31(3):397-404.
2. Yasuda H et al. Failure to prevent progressive dilation of ascending
aorta by aortic valve replacement in patients with bicuspid aortic valve: comparison
with tricuspid aortic valve. Circulation.
2003 Sep 9;108 Suppl 1:II291-4. (full text)
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