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Aortic Dissection

  • Author: Mary C Mancini, MD, PhD, MMM; Chief Editor: John Geibel, MD, DSc, MSc, MA  more...
 
Updated: Dec 02, 2015
 

Practice Essentials

Aortic dissection (see the image below) is defined as separation of the layers within the aortic wall. Tears in the intimal layer result in the propagation of dissection (proximally or distally) secondary to blood entering the intima-media space. Mortality is still high despite advances in diagnostic and therapeutic modalities.

Aortic dissection. Aortic dissection.

Signs and symptoms

Aortic dissection can be rapidly fatal, with many patients dying before presentation to the emergency department or before diagnosis is made in the ED.

No one sign or symptom can positively identify acute aortic dissection. Clinical manifestations include the following:

  • Sudden onset of severe chest pain that often has a tearing or ripping quality (classic symptom)
  • Chest pain may be mild
  • Anterior chest pain: Usually associated with anterior arch or aortic root dissection
  • Neck or jaw pain: With aortic arch involvement and extension into the great vessels
  • Tearing or ripping intrascapular pain: May indicate dissection involving the descending aorta
  • No pain in about 10% of patients
  • Syncope
  • Cerebrovascular accident (CVA) symptoms (eg, hemianesthesia, and hemiparesis, hemiplegia) [1]
  • Altered mental status
  • Numbness and tingling, pain, or weakness in the extremities
  • Horner syndrome (ie, ptosis, miosis, anhidrosis)
  • Dyspnea
  • Hemoptysis
  • Dysphagia
  • Flank pain (with renal artery involvement
  • Abdominal pain (with abdominal aorta involvement)
  • Fever
  • Anxiety and premonitions of death

See Clinical Presentation for more detail.

Diagnosis

The diagnosis of acute aortic dissection requires a high index of suspicion and involves the following:

  • History and physical examination
  • Imaging studies
  • Electrocardiography
  • Complete blood count, serum chemistry studies, cardiac marker assays

Possible physical examination findings include the following:

  • Hypertension
  • Hypotension
  • Interarm blood pressure differential greater than 20 mm Hg
  • Signs of aortic regurgitation (eg, bounding pulses, wide pulse pressure, diastolic murmurs)
  • Findings suggestive of cardiac tamponade (eg, muffled heart sounds, hypotension, pulsus paradoxus, jugular venous distention, Kussmaul sign)
  • Neurologic deficits (eg, syncope, altered mental status)
  • Peripheral paresthesias
  • Horner syndrome
  • New diastolic murmur
  • Asymmetrical pulses (eg, carotid, brachial, femoral)
  • Progression or development of bruits

Possible laboratory study findings include the following:

  • Leukocytosis: Stress state
  • Decreases in hemoglobin and hematocrit values: Leaking or rupture of the dissection
  • Elevation of the blood urea nitrogen and creatinine levels: Renal artery involvement or prerenal azotemia
  • Elevation of the myocardial muscle creatine kinase isoenzyme, myoglobin, and troponin I and T levels: Myocardial ischemia from coronary artery involvement
  • Lactate dehydrogenase elevation: Hemolysis in the false lumen
  • Smooth muscle myosin heavy-chain assay: Increased levels in the first 24 hours are 90% sensitive and 97% specific for aortic dissection
  • Fibrin degradation product (FDP) elevation: In symptomatic patients, a plasma FDP of 12.6 μg/mL or higher suggests possible aortic dissection with a patent false lumen; an FDP level of 5.6 μg/mL or higher suggests the possibility of dissection with complete thrombosis of the false lumen [2]

Imaging studies

Chest radiography:

  • Initial imaging technique if it is readily available at the bedside
  • Widening of the mediastinum is the classic finding
  • Hemothorax may be evident if the dissection has ruptured

Computed tomography with contrast:

  • The definitive test in most patients with suspicion of aortic dissection [3]
  • Useful only in hemodynamically stable patients
  • Findings help determine whether hypothermic circulatory arrest is necessary for surgery

Echocardiography:

  • Transesophageal echocardiography (TEE) is more accurate than transthoracic echocardiography (TTE) [4]
  • TTE is most useful in ascending aortic dissections
  • TEE is as sensitive and specific as CT scanning and magnetic resonance imaging
  • TEE is strongly dependent on operator experience

MRI:

  • The most sensitive method for diagnosing aortic dissection
  • Specificity is similar to that of CT scanning

Aortography:

  • Has been the diagnostic criterion standard study for aortic dissection
  • Is being replaced by newer, safer imaging modalities

See Workup for more detail.

Management

Acute aortic dissection can be treated surgically or medically. In surgical treatment, the area of the aorta with the intimal tear is usually resected and replaced with a Dacron graft. Endovascular repair is emerging as the preferred treatment for descending aortic dissection.

Medical management includes the following:

  • Decreasing the blood pressure and the shearing forces of myocardial contractility
  • Antihypertensive therapy, including beta blockers, is the treatment of choice for all stable chronic aortic dissections
  • Pain management: Narcotics and opiates are the preferred agents

Emergency surgical correction is the preferred treatment for the following:

  • Stanford type A (DeBakey type I and II) ascending aortic dissection
  • Complicated Stanford type B (DeBakey type III) aortic dissections with specific clinical or radiologic evidence

See Treatment and Medication for more detail.

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Background

Aortic dissection is defined as separation of the layers within the aortic wall. Tears in the intimal layer result in the propagation of dissection (proximally or distally) secondary to blood entering the intima-media space.

An acute aortic dissection (< 2 weeks) is associated with high morbidity and mortality rates. Mortality is highest in the first 7 days; indeed, many patients die before presentation to the emergency department (ED) or before diagnosis is made in the ED. Patients with chronic aortic dissection (>2 weeks) have a better prognosis. The mortality associated with aortic dissection is still high despite advancements in diagnostic and therapeutic modalities.[5, 6]

Although acute aortic dissection classically produces sudden onset of severe chest pain that often has a tearing or ripping quality, no one sign or symptom can positively identify acute aortic dissection. The clinical manifestations are diverse, making the diagnosis difficult and necessitating a high index of suspicion.[5, 7, 6] (See Presentation.) An estimated 38% of acute aortic dissections are missed on initial evaluation.[8, 1, 9]

There are no validated clinical decision rules to help identify acute aortic dissection. The diagnosis is best made when there is high clinical suspicion. A good patient history and physical examination are essential, along with imaging studies, electrocardiography, and laboratory studies (see Workup).

Acute aortic dissection can be treated surgically or medically. In surgical treatment, the area of the aorta with the intimal tear is usually resected and replaced with a Dacron graft. (See the Treatment section and the Medication section.)

For patient education information, see the Heart and Blood Vessels Center, the Circulatory Problems Center, and the Heart Center, as well as Chest Pain.

History of aortic dissection and its repair

The first well-documented case of aortic dissection occurred in 1760, when King George II of England died while straining on the commode. In 1761, the celebrated Italian anatomist Giovanni Battista Morgagni provided the first detailed pathologic description of aortic dissection.

Aortic dissection was associated with a high mortality rate before the introduction of the cardiopulmonary bypass in the 1950s, which led to aortic arch repair and construction. DeBakey performed the first successful operative repair in 1955.

Modern techniques of diagnosing and repairing thoracic aortic dissections transformed the condition from a death sentence to a treatable disorder—as shown by the experience of Dr. DeBakey himself, who developed aortic dissection at age 97, and at age 98 became the oldest patient to survive the surgical procedure he pioneered.[10]

Later advances in the field of stent placement and percutaneous aortic fenestrations have further lowered mortality. However, despite these advances, the mortality associated with aortic dissection remains high, as illustrated by the deaths of Princess Diana, actor John Ritter, and diplomat Richard Holbrooke.[5, 6]

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Anatomy

The aorta is composed of the intima, media, and adventitia. The intima, the innermost layer, is thin, delicate, lined by endothelium, and easily traumatized.

The media is responsible for imparting strength to the aorta and consists of laminated but intertwining sheets of elastic tissue. The arrangement of these sheets in a spiral provides the aorta with its maximum allowable tensile strength. The aortic media contains very little smooth muscle and collagen between the elastic layers and thus has increased distensibility, elasticity, and tensile strength. This contrasts with peripheral arteries, which, in comparison, have more smooth muscle and collagen between the elastic layers.

The outermost layer of the aorta is adventitia. This largely consists of collagen. The vasa vasorum, which supplies blood to the outer half of the aortic wall, lies within the adventitia. The nervi vascularis, bundles of nerve fibers found in the aortic adventitia, are involved in the production of pain, which occurs with acute stretching of the aortic wall from a dissection.[11] .The aorta does not have a serosal layer.

The aorta plays an integral role in the forward circulation of the blood in diastole. During left ventricular contraction, the aorta is distended by blood flowing from the left ventricle, and kinetic energy from the ventricle is transformed into potential energy stored in the aortic wall. During recoil of the aortic wall, this potential energy is converted to kinetic energy, propelling the blood within the aorta to the peripheral vasculature.

The volume of blood ejected into the aorta, the compliance of the aorta, and resistance to blood flow are responsible for the systolic pressures within the aorta. Resistance is mainly due to the tone of the peripheral vessels, although the inertia exerted by the column of blood during ventricular systole also plays a small part.

The aorta has thoracic and abdominal regions. The thoracic aorta is divided into the ascending, arch, and descending segments; the abdominal aorta is divided into suprarenal and infrarenal segments. The ascending aorta is the anterior tubular portion of the thoracic aorta from the aortic root proximally to the innominate artery distally. The ascending aorta is 5 cm long and is made up of the aortic root and an upper tubular segment.

The aortic root consists of the aortic valve, sinuses of Valsalva, and left and right coronary arteries. It extends from the aortic valve to the sinotubular junction and supports the base of the aortic leaflets. The aortic root allows the 3 sinuses of Valsalva to bulge outward, facilitating the full excursion of the leaflets in systole. The left and right coronary arteries arise from these sinuses.

The upper tubular segment of the ascending aorta starts at the sinotubular junction and ends at the beginning of the aortic arch. The ascending aorta lies slightly to the right of the midline, with its proximal portion in the pericardial cavity. Structures around the aorta include the pulmonary artery anteriorly; the left atrium, right pulmonary artery, and right mainstem bronchus posteriorly; and the right atrium and superior vena cava to the right.

The arch of the aorta curves upward between the ascending aorta and descending aorta. The brachiocephalic arteries originate from the aortic arch. Arteries that arise from the aortic arch carry blood to the brain via the left common carotid, innominate, and left subclavian arteries.

The initial part of the aortic arch lies slightly left and in front of the trachea; the arch ends posteriorly to the left of the trachea and esophagus. Inferior to the arch is the pulmonary artery bifurcation, the right pulmonary artery, and the left lung. The recurrent laryngeal nerve passes beneath the distal arch, and the phrenic and vagus nerves lie to the left. The junction between the aortic arch and the descending aorta is called the aortic isthmus. The isthmus is a common site for coarctations and trauma.

The descending aorta extends from the area distal to the left subclavian artery to the 12th intercostal space. Initially, the descending aorta lies in the posterior mediastinum to the left of the course of the vertebral column. It passes in front of the vertebral column in its descent and ends behind the esophagus before passing through the diaphragm at the level of the 12th thoracic vertebra.

The abdominal aorta extends from the descending aorta at the level of the 12th thoracic vertebra to the level of bifurcation at the fourth lumbar vertebra. The splanchnic arteries branch from the abdominal aorta. The thoracoabdominal aorta is the combination of the descending thoracic and abdominal aorta.

With increasing age, the elasticity and distensibility of the aorta decline, thus inducing the increase in pulse pressure observed in elderly individuals. The progression of this process is exacerbated by hypertension, coronary artery disease, or hypercholesterolemia.

Histologically, the loss of distensibility is marked by fragmentation of elastin and the resultant increase in collagen and, thus, a higher collagen-to-elastin ratio. This, along with impairment in flow in the vasa vasorum, may be responsible for the age-related changes. These factors cumulatively lead to increased left ventricular systolic pressure and wall tension with associated increases in end-diastolic pressure and volume.

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Pathophysiology

The aortic wall is exposed to high pulsatile pressure and shear stress (the steep slope of the pressure curve; ie, the water hammer effect), making the aorta particularly prone to injury and disease from mechanical trauma. The aorta is more prone to rupture than any other vessel, especially with the development of aneurysmal dilatation, because its wall tension, as governed by the Laplace law (proportional to the product of pressure and radius), is intrinsically high.

An aortic dissection is a split or partition in the media of the aorta; this split is frequently horizontal or diagonal. An intimal tear connects the media with the aortic lumen, and an exit tear creates a true lumen and a false lumen, resulting in a double-barreled aorta (see the image below).

Aortic dissection. True lumen and false lumen sepa Aortic dissection. True lumen and false lumen separated by an intimal flap.

The true lumen is lined by intima, and the false lumen is within the media. Although the false lumen is within the media, suggesting that it is "lined" with media is misleading; if the aortic dissection becomes chronic, the lining becomes a serosal pseudointima.

The true lumen is frequently smaller than the false lumen, but not invariably. Typically, flow in the false lumen is slower than in the true lumen, and the false lumen often becomes aneurysmal when subjected to systemic pressure. The dissection usually stops at an aortic branch vessel or at the level of an atherosclerotic plaque.

Most classic aortic dissections begin at one of the following three distinct anatomic locations:

  • Approximately 2.2 cm above the aortic root
  • Distal to the left subclavian artery
  • The aortic arch

The most common site of dissection is the first few centimeters of the ascending aorta, with 90% occurring within 10 cm of the aortic valve. The second most common site is just distal to the left subclavian artery. Between 5% and 10% of dissections do not have an obvious intimal tear. These often are attributed to rupture of the aortic vasa vasorum as first described by Krukenberg in 1920.

Keeping the descending aorta in mind is important. The descending aorta is the location of most late clinical events after any dissection of the aorta.[12]

Ascending aortic involvement may result in death from wall rupture, hemopericardium and tamponade, occlusion of the coronary ostia with myocardial infarction, or severe aortic insufficiency. The nervi vascularis (ie, bundles of nerve fibers found in the aortic adventitia) are involved in the production of pain.

Classification

Two major anatomic classification schemes for aortic dissection are the DeBakey and the Stanford systems (see the image below).

Image A represents a Stanford A or a DeBakey type Image A represents a Stanford A or a DeBakey type 1 dissection. Image B represents a Stanford A or DeBakey type II dissection. Image C represents a Stanford type B or a DeBakey type III dissection. Image D is classified in a manner similar to A but contains an additional entry tear in the descending thoracic aorta. Note that a primary arch dissection does not fit neatly into either classification.

DeBakey and coworkers classify aortic dissection into three types, as follows:

  • Type I - The intimal tear occurs in the ascending aorta, but the descending aorta is also involved
  • Type II - Only the ascending aorta is involved
  • Type III - Only the descending aorta is involved; type IIIA originates distal to the left subclavian artery and extends as far as the diaphragm, whereas type IIIB involves the descending aorta below the diaphragm

The Stanford classification specifies two types, as follows:

  • Type A - The ascending aorta is involved (DeBakey types I and II)
  • Type B - The descending aorta is involved (DeBakey type III)

This system also helps delineate treatment. Type A dissections usually must be treated surgically, whereas type B dissections are managed medically under most conditions.[13]

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Etiology

Congenital and acquired factors, alone or in combination, can lead to aortic dissection. Aortic dissection is more common in patients with hypertension, connective tissue disorders, congenital aortic stenosis, or a bicuspid aortic valve,[14] as well as in those with first-degree relatives with a history of thoracic dissection. These diseases affect the media of the aorta and predispose it to dissection.

Congenital causes

Aortopathy may be due to the following heritable diseases:

Acquired conditions

Arterial hypertension is an important predisposing factor for aortic dissection.[6] Of patients with aortic dissection, 70% have elevated blood pressure. Hypertension or pulsatile blood flow can propagate the dissection.

Pregnancy can be a risk factor for aortic dissection, particularly in patients with an underlying anomaly such as Marfan syndrome. An estimated 50% of all cases of aortic dissection that occur in women younger than 40 years are associated with pregnancy. Most cases occur in the third trimester or early postpartum period.

Other acquired causes of aortic dissection include the following:

  • Syphilitic aortitis
  • Deceleration injury possibly with related chest trauma
  • Cocaine use

Cystic medial necrosis

The normal aorta contains collagen, elastin, and smooth muscle cells that contribute the intima, media, and adventitia, which are the layers of the aorta. With aging, degenerative changes lead to breakdown of the collagen, elastin, and smooth muscle and an increase in basophilic ground substance. This condition is termed cystic medial necrosis. Atherosclerosis that causes occlusion of the vasa vasorum also produces this disorder. Cystic medial necrosis is the hallmark histologic change associated with dissection in those with Marfan syndrome.

Cystic medial necrosis was first described by Erdheim in 1929. Sources disagree over the accuracy of this term in elderly patients because the true histopathologic changes are neither cystic nor necrotic. Researchers have used the term cystic medial degeneration.

Early on, cystic medial necrosis described an accumulation of basophilic ground substance in the media with the formation of cystlike pools. The media in these focal areas may show loss of cells (ie, necrosis). This term still is used commonly to describe the histopathologic changes that occur.

Iatrogenic causes

Iatrogenic aortic dissection can result from cardiologic procedures such as the following:

  • Aortic and mitral valve replacements
  • Coronary artery bypass graft surgery
  • Percutaneous catheter placement (eg, cardiac catheterization, percutaneous transluminal coronary angioplasty)

Aortic dissection occurs when the layers are split in the process of cannulation or aortotomy.

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Epidemiology

In the United States, aortic dissection is an uncommon disease. The true frequency of aortic dissection is difficult to estimate, and most estimates are based on autopsy studies. Evidence of aortic dissection is found in 1-3% of all autopsies (1 in 350 cadavers).[15] The incidence of aortic dissection is estimated to be 5-30 cases per 1 million people per year. Aortic dissection occurs once per 10,000 patients admitted to the hospital; approximately 2000 new cases are reported each year in the United States.[16]

Aortic dissection is more common in blacks than in whites and is less common in Asians than in whites. Also, it is more common in males than females, with a male-to-female ratio of 2-3:1.

Approximately 75% of dissections occur in those aged 40-70 years, with a peak in the range of 50-65 years.[6] Patients with Marfan syndrome present earlier, usually in the third and fourth decades of life.

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Prognosis

Hospital-based mortality for aortic dissection is approximately 30%. Patients with type A aortic dissection who undergo surgical treatment have a 30% mortality; patients who receive medical treatment have a 60% mortality. Comorbidities and advanced aged can pose a contraindication to surgery in selected patients. Medically treated patients with type B dissection have a 10% mortality; surgically treated patients with type B dissection have a 30% mortality.

An acute aortic dissection (< 2 weeks) is associated with high morbidity and mortality rates (highest mortality in the first 7 days). From 1% to 2% of patients with aortic dissection die per hour for the first 24-48 hours. Patients with chronic aortic dissection (>2 weeks) have a better prognosis.

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Contributor Information and Disclosures
Author

Mary C Mancini, MD, PhD, MMM Professor and Chief of Cardiothoracic Surgery, Department of Surgery, Louisiana State University School of Medicine in Shreveport

Mary C Mancini, MD, PhD, MMM is a member of the following medical societies: American Association for Thoracic Surgery, American College of Surgeons, American Surgical Association, Society of Thoracic Surgeons, Phi Beta Kappa

Disclosure: Nothing to disclose.

Chief Editor

John Geibel, MD, DSc, MSc, MA Vice Chair and Professor, Department of Surgery, Section of Gastrointestinal Medicine, and Department of Cellular and Molecular Physiology, Yale University School of Medicine; Director, Surgical Research, Department of Surgery, Yale-New Haven Hospital; American Gastroenterological Association Fellow

John Geibel, MD, DSc, MSc, MA is a member of the following medical societies: American Gastroenterological Association, American Physiological Society, American Society of Nephrology, Association for Academic Surgery, International Society of Nephrology, New York Academy of Sciences, Society for Surgery of the Alimentary Tract

Disclosure: Received royalty from AMGEN for consulting; Received ownership interest from Ardelyx for consulting.

Acknowledgements

Ali Hmidi, MD Staff Physician, Department of Internal Medicine, Brooklyn Hospital Center, Cornell University

Disclosure: Nothing to disclose.

Sateesh Kesari, MBBS, MD Fellow in Cardiovascular Medicine, New York Presbyterian Hospital/The Brooklyn Hospital Center Program, Weill Cornell Medical College of Cornell University

Sateesh Kesari, MBBS, MD is a member of the following medical societies: American College of Cardiology, American Medical Assocation, American Society of Echocardiography, and American Society of Nuclear Cardiology

Disclosure: Nothing to disclose.

Oladayo Adisa Osinuga Sr, MBBS Attending Physician, Department of Internal Medicine, Atlanta Medical Center

Oladayo Adisa Osinuga Sr, MBBS is a member of the following medical societies: American College of Physicians-American Society of Internal Medicine and American Medical Association

Disclosure: Nothing to disclose.

Ramachandra C Reddy, MD Associate Director, Assistant Professor, Department of Surgery, Division of Cardiothoracic Surgery, State University of New York-Downstate Medical Center

Ramachandra C Reddy, MD is a member of the following medical societies: American College of Cardiology, American College of Chest Physicians, American Medical Association, American Society for Artificial Internal Organs, and Society of Thoracic Surgeons

Disclosure: Nothing to disclose.

Sarath Reddy, MD Associate Director of Cardiac Care Unit, Department of Cardiology, The Brooklyn Hospital Center, Weill Medical College of Cornell University

Sarath Reddy, MD is a member of the following medical societies: American College of Cardiology

Disclosure: Nothing to disclose.

Benson B Roe, MD Emeritus Chief, Division of Cardiothoracic Surgery, Emeritus Professor, Department of Surgery, University of California at San Francisco Medical Center

Benson B Roe, MD is a member of the following medical societies: Alpha Omega Alpha, American Association for Thoracic Surgery, American College of Cardiology, American College of Surgeons, American Heart Association, American Medical Association, American Society for Artificial Internal Organs, American Surgical Association, California Medical Association, Society for Vascular Surgery, Society of Thoracic Surgeons, and Society of University Surgeons

Disclosure: Nothing to disclose.

Vincent Lopez Rowe, MD Associate Professor of Surgery, Department of Surgery, Division of Vascular Surgery, University of Southern California Medical Center

Vincent Lopez Rowe, MD is a member of the following medical societies: American College of Surgeons, American Heart Association, Pacific Coast Surgical Association, Peripheral Vascular Surgery Society, Society for Clinical Vascular Surgery, Society for Vascular Surgery, and Western Vascular Surgical Society

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

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Aortic dissection. CT scan showing a flap (right side of image).
Aortic dissection. True lumen versus false lumen in an intimal flap.
Aortic dissection. Left subsegmental atelectasis and left pleural effusion. Flap at lower right of image.
Aortic dissection. Significant left pleural effusion.
Aortic dissection. CT scan showing a flap (center of image).
Aortic dissection. CT scan showing a flap (center of image).
Aortic dissection. CT scan showing a flap.
Aortic dissection. CT scan showing a flap.
Aortic dissection. Mediastinal widening.
Aortic dissection. CT scan showing a flap.
Aortic dissection. CT scan showing a flap.
Aortic dissection. CT scan showing a flap.
Aortic dissection. Thrombus and a patent lumen.
Aortic dissection. Thrombus.
Aortic dissection. True lumen and false lumen separated by an intimal flap.
Aortic dissection. Mediastinal widening.
Aortic dissection. CT scan showing a flap.
Aortic dissection. Intimal flap and left pleural effusion.
Image A represents a Stanford A or a DeBakey type 1 dissection. Image B represents a Stanford A or DeBakey type II dissection. Image C represents a Stanford type B or a DeBakey type III dissection. Image D is classified in a manner similar to A but contains an additional entry tear in the descending thoracic aorta. Note that a primary arch dissection does not fit neatly into either classification.
Aortic dissection.
Chest radiograph of a patient with aortic dissection. Image courtesy of Dr. K. London, University of California at Davis Medical Center.
Chest radiograph of a patient with aortic dissection presenting with hemothorax.
Chest radiograph demonstrating widened mediastinum in a patient with aortic dissection.
Angiogram demonstrating dissection of the aorta in a patient with aortic dissection presenting with hemothorax.
Electrocardiogram of a patient presenting to the ED with chest pain; this patient was diagnosed with aortic dissection.
Patient with an ascending type A aortic dissection showing the intimal flap. Image courtesy of Kaiser-Permanente.
Patient with an ascending type A aortic dissection showing the intimal flap. Image courtesy of Kaiser-Permanente.
Patient with an ascending type A aortic dissection showing the intimal flap. Image courtesy of Kaiser-Permanente.
Patient with an ascending type A aortic dissection showing the intimal flap. Image courtesy of Kaiser-Permanente.
Patient with a type A aortic dissection involving the ascending and descending aorta. Image courtesy of Kaiser-Permanente.
Patient with a type A aortic dissection involving the ascending and descending aorta. Image courtesy of Kaiser-Permanente.
Patient with a type A aortic dissection involving the ascending and descending aorta. Image courtesy of Kaiser-Permanente.
Patient with a type A aortic dissection involving the ascending and descending aorta. Image courtesy of Kaiser-Permanente.
Patient showing a type B aortic dissection with extravasation of blood into the pleural cavity. Image courtesy of Kaiser-Permanente.
Patient showing a type B aortic dissection with extravasation of blood into the pleural cavity. Image courtesy of Kaiser-Permanente.
Patient showing a type B aortic dissection with extravasation of blood into the pleural cavity. Image courtesy of Kaiser-Permanente.
Patient showing a type B aortic dissection with extravasation of blood into the pleural cavity. Image courtesy of Kaiser-Permanente.
 
 
 
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