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Aortic Aneurysm: Symptoms, Diagnosis and Modern Treatment Methods

··10 mins
Assoc. Prof. Dr. Habib ÇİL
Author
Assoc. Prof. Dr. Habib ÇİL
Istanbul University Faculty of Medicine graduate, Akdeniz University Cardiology specialization. Expert in interventional cardiology, coronary angioplasty and TAVI.
Table of Contents
This content has been prepared for informational purposes to protect public health, in compliance with the regulations of the Ministry of Health of the Republic of Turkey and medical ethical rules. It does not provide any diagnosis, treatment guarantees, or specific medical advice. Please consult a qualified healthcare provider for the most accurate information.
An aortic aneurysm is a balloon-like enlargement of the aorta, the body’s main artery, due to weakening of the vessel wall. This serious condition can progress silently and carries rupture risk but can be controlled with early diagnosis and appropriate treatment. This comprehensive guide examines aortic aneurysm types, symptoms, risk factors, diagnostic methods, and current treatment options.

What is an Aortic Aneurysm?
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The aorta is the main artery that emerges from the heart and distributes oxygenated blood throughout the body. The aortic wall consists of three layers: intima (inner layer), media (middle layer), and adventitia (outer layer). An aortic aneurysm is the enlargement of the aorta by at least 50% of its normal diameter due to weakening of these wall layers.

Anatomical Sections of the Aorta
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Ascending Aorta: First segment emerging from the heart, origin of coronary arteries.

Aortic Arch: Curved section giving branches to the brain and arms.

Descending Thoracic Aorta: Downward course within the thoracic cavity.

Abdominal Aorta: Section below the diaphragm within the abdominal cavity.

Aneurysm Types
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By Shape:

  • Fusiform (Spindle-shaped): Symmetric enlargement around the entire circumference
  • Saccular (Sac-like): Asymmetric protrusion from one area of the wall

By Location:

  • Thoracic Aortic Aneurysm (TAA): Affects the aorta in the chest region
  • Abdominal Aortic Aneurysm (AAA): Affects the aorta in the abdominal region (75-80%)
  • Thoracoabdominal Aortic Aneurysm: Involves both regions

Causes and Risk Factors
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Structural and Genetic Causes
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Connective Tissue Disorders:

  • Marfan syndrome
  • Ehlers-Danlos syndrome (vascular type)
  • Loeys-Dietz syndrome

Familial Predisposition:

  • First-degree relatives with aneurysm history
  • Genetic polymorphisms (FBN1, TGFBR1/2 genes)

Acquired Causes
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Atherosclerosis (Artery Hardening):

  • Most common cause (80-90%)
  • Lipid accumulation, inflammation, smooth muscle cell loss
  • Particularly strong association with abdominal aortic aneurysm

Hypertension:

  • Chronic pressure overload
  • Degeneration of the medial layer
  • Accelerates aneurysm growth

Infections (Mycotic Aneurysm):

  • Complication of bacterial endocarditis
  • Salmonella, Staphylococcus aureus
  • Rapid progression and rupture risk

Trauma:

  • Blunt or penetrating injuries
  • Motor vehicle accidents, falls from height
  • Pseudoaneurysm development

Vasculitides:

  • Giant cell arteritis
  • Takayasu arteritis
  • Behçet’s disease

Risk Factors
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Non-modifiable Risk Factors:

  • Age: Risk increases over 65 years
  • Gender: 4-5 times more common in men
  • Genetics: Family history (risk increases 2-4 fold)
  • Race/Ethnicity: More common in Caucasians

Modifiable Risk Factors:

  • Smoking: Strongest risk factor (risk increases 5-6 fold)
  • Hypertension: Uncontrolled high blood pressure
  • Hypercholesterolemia: High LDL, low HDL
  • Obesity: Body mass index >30
  • Sedentary Lifestyle: Lack of physical activity

Aortic Aneurysm Symptoms
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Asymptomatic Period
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The great majority of aneurysms (70-80%) are asymptomatic. They are discovered incidentally during imaging studies or routine examinations.

Thoracic Aortic Aneurysm Symptoms
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Compression Findings:

  • Trachea and bronchial compression: Cough, shortness of breath, stridor
  • Esophageal compression: Swallowing difficulty (dysphagia)
  • Recurrent laryngeal nerve compression: Hoarseness
  • Superior vena cava compression: Facial and neck swelling

Pain:

  • Chest pain (often radiating to the back)
  • Sharp, tearing sensation pain (suspicion of dissection)
  • Constant, dull pain (growing aneurysm)

Other Symptoms:

  • Aortic insufficiency (murmur, shortness of breath)
  • Stroke or ischemia due to clot embolization

Abdominal Aortic Aneurysm Symptoms
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Early Stage:

  • Mostly asymptomatic
  • Pulsating sensation in abdomen
  • Mild abdominal or back pain

Advanced Stage:

  • Significant abdominal pain (may radiate to back)
  • Palpable mass (especially in thin patients)
  • Loss of appetite, nausea (gastrointestinal compression)

Emergency Symptoms (Pre-rupture or Rupture):

  • Sudden, severe abdominal/back pain (“tearing sensation”)
  • Hypotension, tachycardia
  • Syncope (fainting)
  • Shock findings (cold sweat, pallor, altered consciousness)
Emergency: Sudden onset of severe chest, back, or abdominal pain, shortness of breath, fainting, or shock symptoms may indicate aortic aneurysm rupture or dissection. Immediately call 112 emergency services!

Diagnostic Methods
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Physical Examination
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Abdominal Aortic Aneurysm:

  • Palpable enlarged, pulsatile mass
  • Bruit (on auscultation)
  • Evaluation of distal pulses

Thoracic Aortic Aneurysm:

  • Chest wall asymmetry
  • Murmur (aortic insufficiency)
  • Focal neurological deficit (embolism)

Imaging Methods
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Ultrasonography (USG):

  • Gold standard for abdominal aortic aneurysm screening and follow-up
  • Non-invasive, radiation-free, inexpensive
  • Diameter measurement, thrombus presence
  • Limited thoracic imaging

Computed Tomography Angiography (CT Angio):

  • Most valuable method for diagnosis and treatment planning
  • 3D reconstruction capability
  • Aneurysm diameter, length, neck, related vessels
  • Measurements for endovascular treatment planning
  • Contrast agent and radiation exposure disadvantages

Magnetic Resonance Angiography (MR Angio):

  • Radiation-free alternative
  • Non-contrast (TOF) or contrast-enhanced techniques
  • Can show wall characteristics in connective tissue diseases
  • Metal implant, claustrophobia limitations

Transesophageal Echocardiography (TEE):

  • Detailed imaging for thoracic aorta evaluation
  • Ideal for aortic valve and ascending aorta segment
  • Invasive procedure requiring sedation

Conventional Angiography:

  • Now used more during treatment than diagnosis
  • Hemodynamic evaluation capability
  • Invasive, contrast agent risk

Screening Recommendations
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Abdominal Aortic Aneurysm:

  • USPSTF Recommendation: One-time ultrasonography screening in men aged 65-75 who have ever smoked at least 100 cigarettes
  • ACC/AHA Recommendation: Men aged 65-75 who smoke or have family history; women aged 65-75 who smoke or have family history
  • Family History: Screening at age 65 for those with first-degree relative with AAA

Thoracic Aortic Aneurysm:

  • Regular echocardiography/TEE in Marfan syndrome, Ehlers-Danlos, or other connective tissue disorders
  • Patients with bicuspid aortic valve
  • Those with family history

Treatment Approaches
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Treatment decisions are individualized based on aneurysm characteristics, patient clinical status, and risk factors.

Medical Therapy and Monitoring
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Small Aneurysms (AAA <5.5 cm, TAA <5.5-6.0 cm):

  • Regular imaging follow-up
  • Diameter measurement every 6-12 months with CT or USG
  • More frequent monitoring if growth rate >0.5 cm/year

Risk Factor Modification:

  • Smoking Cessation: Most critical intervention
  • Blood Pressure Control: Target <130/80 mmHg
  • Statin Therapy: LDL <70 mg/dL (plaque stabilization)
  • Beta Blockers: Slows progression in Marfan syndrome
  • ACE Inhibitors/ARBs: TGF-β inhibition in connective tissue diseases

Surgical Treatment Indications
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Absolute Indications:

  • Symptomatic aneurysm (pain, compression findings)
  • Suspected rupture or dissection
  • Rapid growth (>0.5 cm/6 months)
  • Abdominal aortic aneurysm ≥5.5 cm (men), ≥5.0 cm (women)
  • Thoracic aortic aneurysm ≥5.5-6.0 cm (without connective tissue disease)

Relative Indications:

  • Family history of rupture
  • Female patients (higher rupture risk)
  • Aneurysm morphology (saccular, asymmetric)
  • Young patient (long life expectancy)

Open Surgical Repair
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Abdominal Aortic Aneurysm:

  • Transperitoneal or retroperitoneal approach
  • Aneurysm opened and replaced with graft
  • 95-98% success rate
  • Hospital stay: 5-10 days
  • Full recovery: 6-12 weeks

Thoracic Aortic Aneurysm:

  • Sternotomy or thoracotomy
  • Often requires cardiopulmonary bypass
  • Hypothermic circulatory arrest (brain protection)
  • Spinal protection techniques (CSF drainage)

Endovascular Therapies
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EVAR (Endovascular Aneurysm Repair):

  • Minimally invasive alternative for abdominal aortic aneurysm
  • Stent-graft placement via catheters through groin arteries
  • Anesthesia: Usually spinal/epidural
  • Hospital stay: 2-3 days
  • Recovery: 2-4 weeks
  • Requires long-term follow-up (endoleak monitoring)

TEVAR (Thoracic Endovascular Aortic Repair):

  • Endovascular approach for thoracic aortic aneurysms
  • More complex anatomical requirements
  • Higher spinal ischemia risk
  • Carotid-subclavian bypass may be needed if left subclavian artery coverage is required

Mixed/Hybrid Procedures:

  • Open surgery + endovascular combinations
  • Debranching + TEVAR for arch aneurysms
  • Visceral debranching + EVAR for thoracoabdominal aneurysms

New Technologies and Developments
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Branched and Fenestrated Stent-Grafts:

  • Increase EVAR/TEVAR applicability in complex anatomy
  • Preservation of renal, mesenteric, arch branches
  • Custom-made production

Flow Diverter Stents:

  • For saccular aneurysms
  • Diverts blood flow from aneurysm neck to promote thrombosis

Biological Grafts and Tissue Engineering:

  • Infected (mycotic) aneurysms
  • Homograft or bovine/pericardial grafts

Complications and Management
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Open Surgical Complications
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Early Period:

  • Bleeding, infection
  • Heart attack, arrhythmia
  • Acute kidney failure
  • Spinal ischemia (paraplegia risk 5-8% in thoracoabdominal)
  • Colon ischemia (inferior mesenteric artery coverage)

Late Period:

  • Graft infection
  • Aortoenteric fistula
  • Anastomotic aneurysm
  • Graft occlusion

Endovascular Treatment Complications
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Endoleak (Blood Leak Around Stent-Graft):

  • Type I: Proximal/distal attachment site leak (urgent intervention)
  • Type II: Retrograde flow from lumbar/inferior mesenteric arteries (monitoring)
  • Type III: Stent-graft component separation (intervention)
  • Type IV: Graft porosity (resolves spontaneously)
  • Type V: Endotension (diameter increase, no leak)

Other Complications:

  • Stent migration, fracture
  • Access artery injury (dissection, rupture)
  • Renal artery coverage (kidney failure)
  • Spinal ischemia (3-10% in TEVAR)
  • Microembolism (blue toe syndrome)

Rupture and Dissection
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Aortic Dissection:

  • Separation of aortic wall layers
  • Stanford classification (Type A: ascending aorta involvement - emergency surgery; Type B: descending aorta only - medical/endovascular)
  • Sudden tearing sensation pain
  • Organ malperfusion (kidney, bowel, extremity)

Rupture Management:

  • Emergency hemodynamic stabilization
  • Blood transfusion protocols
  • Emergency EVAR or open surgery
  • Mortality: 80-90% (pre-hospital after rupture), 40-50% (with surgical intervention)

Follow-up and Lifestyle Recommendations
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Post-treatment Follow-up
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After EVAR/TEVAR:

  • 30 days: Clinical evaluation, CT angio
  • 6 months, 12 months: CT angio
  • Annually thereafter: CT angio or USG/Duplex
  • Monitoring for endoleak, migration, aneurysm size

After Open Surgery:

  • 30 days: Clinical evaluation
  • 6 months, 12 months: USG/CT (graft function, anastomosis)
  • Every 2-3 years thereafter: Imaging

Lifestyle Modifications
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Exercise Recommendations:

  • Regular moderate-intensity aerobic exercise (walking, swimming)
  • Avoid heavy lifting (especially Valsalva maneuver)
  • Avoid activities that suddenly raise blood pressure

Nutrition:

  • Mediterranean diet (olive oil, vegetables, fruit, fish)
  • Salt restriction (<5 g/day)
  • Saturated fat and cholesterol limitation

Medication Adherence:

  • Regular use of antihypertensive medications
  • Statin therapy (plaque stabilization)
  • Antiplatelet therapy (if stent present)

Regular Check-ups:

  • Blood pressure monitoring (home measurement)
  • Lipid profile, kidney function tests
  • Cardiology/vascular surgery follow-up

Frequently Asked Questions (FAQ)
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What is an aortic aneurysm and why is it dangerous? +

What are the symptoms of aortic aneurysm? +

How is aneurysm diagnosed? +

When should an aneurysm be treated? +

What is the difference between EVAR and open surgery? +

Can aortic aneurysm be prevented? +

What is life like after aneurysm treatment? +

What are the differences between thoracic and abdominal aortic aneurysm? +

When to See a Doctor?
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Seek medical help without delay if you experience:

  1. New or changing pain: Chest, back, or abdominal pain
  2. Shortness of breath, cough, hoarseness
  3. Swallowing difficulty
  4. Pulsating sensation or mass in abdomen
  5. Sudden severe pain (suspicion of rupture/dissection)
  6. Dizziness, fainting, shock symptoms
  7. Family history of aortic aneurysm or rupture for screening
  8. Smoking history + over 65 years in men for screening

Especially if you are in a high-risk group (smoking, hypertension, family history), regular cardiovascular evaluation is critical for early diagnosis and complication prevention.


Important Note: Aortic aneurysm can progress silently but can be effectively managed when diagnosed early. Modern treatment methods achieve high success rates, allowing patients to return to normal life. If you have risk factors or experience suspicious symptoms, consult a cardiology specialist for comprehensive evaluation.

Schedule an Appointment
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You can schedule an appointment for aortic aneurysm evaluation, screening, or information about treatment options.

Schedule Appointment

⚠️ Disclaimer: This content is for informational purposes only. Please consult your doctor for diagnosis and treatment.