Aortic root dilatation
Aortic Root Dilatation
Aortic root dilatation refers to the enlargement of the aortic root, which is the section of the aorta closest to and attached to the heart. This condition can lead to serious cardiovascular complications, including aortic regurgitation and aortic dissection. Understanding the causes, symptoms, diagnosis, and treatment options for aortic root dilatation is crucial for medical professionals and patients alike.
Anatomy and Function[edit | edit source]
The aortic root is the portion of the aorta that connects to the heart's left ventricle. It includes the aortic valve, the sinuses of Valsalva, and the proximal ascending aorta. The aortic root plays a critical role in maintaining proper blood flow from the heart to the rest of the body.
Causes[edit | edit source]
Aortic root dilatation can be caused by a variety of factors, including:
- Genetic Disorders: Conditions such as Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome are known to cause connective tissue abnormalities that can lead to aortic root dilatation.
- Hypertension: Chronic high blood pressure can put stress on the aortic wall, leading to dilatation.
- Aging: As individuals age, the elasticity of the aortic wall can decrease, resulting in dilatation.
- Atherosclerosis: The buildup of plaque in the arteries can weaken the aortic wall.
Symptoms[edit | edit source]
Many patients with aortic root dilatation are asymptomatic, especially in the early stages. However, as the condition progresses, symptoms may include:
- Chest pain or discomfort
- Shortness of breath
- Palpitations
- Fatigue
Diagnosis[edit | edit source]
Diagnosis of aortic root dilatation typically involves:
- Echocardiography: An ultrasound of the heart that can measure the size of the aortic root and assess valve function.
- CT or MRI Scans: These imaging techniques provide detailed images of the aorta and can help in assessing the extent of dilatation.
- Genetic Testing: In cases where a genetic disorder is suspected, testing can confirm the diagnosis.
Treatment[edit | edit source]
Treatment options depend on the size of the dilatation and the presence of symptoms:
- Medical Management: Includes blood pressure control with medications such as beta-blockers or angiotensin receptor blockers.
- Surgical Intervention: In cases of significant dilatation or risk of complications, surgical repair or replacement of the aortic root may be necessary.
Prognosis[edit | edit source]
The prognosis for patients with aortic root dilatation varies based on the underlying cause and the effectiveness of treatment. Regular monitoring and appropriate management can significantly improve outcomes.
Also see[edit | edit source]
Cardiovascular disease A-Z
Most common cardiac diseases
- Cardiac arrhythmia
- Cardiogenetic disorders
- Cardiomegaly
- Cardiomyopathy
- Cardiopulmonary resuscitation
- Chronic rheumatic heart diseases
- Congenital heart defects
- Heart neoplasia
- Ischemic heart diseases
- Pericardial disorders
- Syndromes affecting the heart
- Valvular heart disease
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
A[edit source]
- Accelerated idioventricular rhythm
- Acute decompensated heart failure
- Arteriosclerotic heart disease
- Athletic heart syndrome
- Atrial flutter
- Atrioventricular fistula
- Cardiovascular disease in Australia
- Autoimmune heart disease
B[edit source]
C[edit source]
- Ebb Cade
- Cardiac allograft vasculopathy
- Cardiac amyloidosis
- Cardiac asthma
- Cardiac tamponade
- Cardiogenic shock
- Cardiogeriatrics
- Cardiorenal syndrome
- Cardiotoxicity
- Carditis
- Coronary artery aneurysm
- Coronary artery anomaly
- Coronary artery disease
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- Coronary occlusion
- Coronary steal
- Coronary thrombosis
- Coronary vasospasm
- Cœur en sabot
- Coxsackievirus-induced cardiomyopathy
D[edit source]
E[edit source]
H[edit source]
- Heart attack
- Heart failure
- Heart failure with preserved ejection fraction
- Heart to Heart (1949 film)
- High-output heart failure
- Hyperdynamic precordium
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
I[edit source]
- Idiopathic giant-cell myocarditis
- Interventricular dyssynchrony
- Intraventricular dyssynchrony
- Isolated atrial amyloidosis
K[edit source]
L[edit source]
M[edit source]
- Mydicar
- Myocardial bridge
- Myocardial disarray
- Myocardial rupture
- Myocardial scarring
- Myocardial stunning
- Myocarditis
N[edit source]
O[edit source]
P[edit source]
- Papillary fibroelastoma
- Pathophysiology of heart failure
- Postpericardiotomy syndrome
- Pulmonary vein stenosis
R[edit source]
S[edit source]
- Saturated fat and cardiovascular disease
- SCAR-Fc
- Shone's syndrome
- Strain pattern
- Subacute bacterial endocarditis
- Sudden cardiac death of athletes
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
T[edit source]
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