An asymptomatic 12-year-old boy with Marfan syndrome presented for routine follow-up and to establish cardiology care at our institution. His previous echocardiograms were reportedly normal. An electrocardiogram showed normal results. A routine echocardiogram revealed an ectatic proximal right coronary artery. Subsequent coronary computed tomographic angiograms showed a fusiform aneurysm beginning at the right coronary artery ostium (Fig 1). The aneurysm was 8 mm long and 5.2 cm in diameter (Z score, +3.8). The patient was prescribed low-dose aspirin.

Fig. 1

Computed tomographic angiograms. A) Curved multiplanar reformatted image shows a mildly dilated fusiform aneurysm (arrow) beginning at the right coronary artery ostium. B) Three-dimensional volume-rendered image shows the 8-mm-long, 5.2-mm-diameter aneurysm (arrow).

Fig. 1

Computed tomographic angiograms. A) Curved multiplanar reformatted image shows a mildly dilated fusiform aneurysm (arrow) beginning at the right coronary artery ostium. B) Three-dimensional volume-rendered image shows the 8-mm-long, 5.2-mm-diameter aneurysm (arrow).

Close modal

Marfan syndrome is an autosomal dominant genetic disease caused by a mutation in the fibrillin FBN1 gene (estimated prevalence, 1 in 3,000–10,000 people).1  The gene is integral to elastic connective tissue, so patients with Marfan syndrome often have related abnormalities, especially cardiovascular, skeletal, and ocular.2  Chief among the cardiovascular complications is aortic root dilation, which carries the risk of aortic dissection and may suggest a need for prophylactic aortic root replacement. In Marfan syndrome, coronary artery involvement is usually a consequence of aortic dissection, and isolated coronary artery aneurysms are rare3 ; to our knowledge, ours is only the second reported case in a pediatric patient.4 

Routine coronary monitoring with the use of echocardiography and other imaging methods is important in patients with Marfan syndrome, including children, because patients who have coronary aneurysms are often asymptomatic.5  Detecting an aneurysm will enable early treatment and possibly improve the patient's overall prognosis.

Section editor: Raymond F. Stainback, MD

1.
McKusick
VA.
The defect in Marfan syndrome
.
Nature
1991
;
352
(
6333
):
279
81
.
2.
Mellody
KT,
Freeman
LJ,
Baldock
C,
Jowitt
TA,
Siegler
V,
Raynal
BDE,
et al.
Marfan syndrome-causing mutations in fibrillin-1 result in gross morphological alterations and highlight the structural importance of the second hybrid domain
.
J Biol Chem
2006
;
281
(
42
):
31854
62
.
3.
Donato
R,
David
E,
Blandino
A,
Gaeta
M,
Spinelli
D,
Ascenti
G.
Coronary involvement in Marfan syndrome: the role of electrocardiographically gated computed tomography angiography
.
J Cardiovasc Echogr
2017
;
27
(
2
):
64
5
.
4.
Williams-Phillips
S.
Marfan's syndrome: pre-pubertal aortic rupture with left coronary artery aneurysms and fistulas
.
West Indian Med J
2012
;
61
(
9
):
937
40
.
5.
Abou Sherif
S,
Ozden Tok
O,
Taskoylu
O,
Goktekin
O,
Kilic
ID.
Coronary artery aneurysms: a review of the epidemiology, pathophysiology, diagnosis and treatment
.
Front Cardiovasc Med
2017
;
4
:
24
.