X-Ray
USG
CT Scan
PET/CT
MRI
Aortography
Intravascular Ultrasound
ACUTE AORTIC SYNDROMES
Emergency conditions
eventually leads to a breakdown of the intima
and media
tear or an ulcer allows blood to penetrate from the
aortic lumen into the media
when a rupture of vasa vasorum causes a bleed
within the media
IMH, PAU, or in separation of aortic wall layers
Acute aortic dissection
Intramural haematoma
Aortic Pseudoaneurysm
Symptoms
may be similar to those of AD,
Surgery
7. IATROGENIC AORTIC DISSECTION
(i) catheter-based coronary procedures,
(ii) cardiac surgery,
Often Asymptomatic
Less with clinical signs of compression,
chest pain, an aortic valve murmur
In patients with Marfan syndrome, the TAA
growth is on average at 0.5–1 mm/year,
In Loeys-Dietz syndrome (LDS) can grow
more than 10 mm/year, mean age of death
26 years
Descending aorta grow faster (at 3
mm/year) than in ascending aorta (at 1
mm/year)
Evaluation
Echo
X-Ray
CT scan
1. Size
2. Co-existing aorta disease (IMH, PAU,
aneurysmal branch vessel)
ABDOMINAL AORTIC ANEURYSM
CT scan
MRI
Small abdominal aortic aneurysms (30-54
mm)
Conservative : Beta Blocker, ACE inhibitor,
antiplatelet, statin.
Recommendation for asymptomatic AAA
GENETIC DISEASE OF AORTA
1. Turner syndrome
Partial or complete monosomy of the X
chromosome (karyotype 45X0)
A generalized dilation of major vessels is
observed, notably the aorta, the brachial, and
carotid arteries.
management
imaging (echocardiogram and thoracic MRI) with
CV risk assessment.
FU:
with TTE every 3–5 years for low risk,
thoracic MRI every 3–5 years for moderate risk,
and
referral to a cardiologist with 1–2-yearly thoracic
MRI for high-risk patients.
2. Marfan syndrome
Heritable connective tissue disorder, AD
bifid uvula,
palpable collaterals
Echo:
Site, structure, and extent of coarctation, EF,
and hypertrophy, and aortic and supra-aortic
vessel diameters
MRI
CT scan
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