Thoracic aorta: acute syndromes.
Article Type: Report
Subject: Dissecting aneurysm (Diagnosis)
Dissecting aneurysm (Prognosis)
Aorta, Thoracic (Diseases)
Magnetic resonance imaging (Usage)
CT imaging (Usage)
Authors: Shiau, Maria C.
Godoy, Myrna C.B.
de Groot, Patricia M.
Ko, Jane P.
Pub Date: 01/01/2010
Publication: Name: Applied Radiology Publisher: Anderson Publishing Ltd. Audience: Academic Format: Magazine/Journal Subject: Health Copyright: COPYRIGHT 2010 Anderson Publishing Ltd. ISSN: 0160-9963
Issue: Date: Jan-Feb, 2010 Source Volume: 39 Source Issue: 1-2
Accession Number: 231310692
Full Text: The term acute aortic syndrome (AAS) refers to a spectrum of life-threatening aortic emergencies. (1) These include nontraumatic entities such as aortic dissection, intramural hematoma (IMH), penetrating atherosclerotic ulcer and rupture of the thoracic aorta due to aneurysm (Figure 1). The incidence of AAS is 2.6 to 3.5 cases per 100,000 instances per year. Two thirds of patients are male, and the average age of affected patients is 63 years. (2)

Historically, acute aortic syndromes are attributed to sequela of chronic hypertension, atherosclerosis, and weakening of the aortic media, predisposing to rupture of the vasa vasorum. Recently, there are theories elucidating causal relationships linking aortic ulceration, IMH and aortic dissection. (3)

The presentation of acute aortic injury is usually acute chest pain described as severe, tearing and migratory. Anterior chest, neck and throat pain mimicking angina may be secondary to abnormalities related to the ascending aorta, whereas back and abdominal pain often indicate descending aortic injury. Syncope suggests development of complications such as cardiac tamponade, obstruction of cerebral vessels or activation of cerebral baroreceptors. (2,4)

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Aortic imaging has dramatically changed over the past 20 years. Previously, diagnosis relied on chest radiography and catheter angiography. However, the sensitivity of chest radiographs for acute aortic syndrome is limited and now multidetector CT (MDCT) enables noninvasive diagnosis of AAS without invasive catheter angiography. Magnetic resonance imaging (MRI) has higher sensitivity and specificity but is less practical in the group of patients assessed for acute aortic symptoms who are potentially unstable and critically ill.

The MDCT protocol approaches 100% sensitivity and specificity (4) and is accepted as first-line imaging for suspected acute aortic disease. CT imaging (Table 1) consists of pre-contrast and arterial-phase imaging using bolus tracking to optimize aortic enhancement.

Precontrast unenhanced scans may be performed using a low-dose technique (decreased mAs) to delineate calcifications and detect IMH. For contrast enhancement, a premonitoring CT section is selected through the aortic arch based on the frontal scout image. A region of interest is placed within the lumen of the thoracic aorta, and the scan is triggered after a designated threshold in Hounsfield units (HU) is reached during dynamic imaging. In patients with acute aortic abnormality involving the distal descending aorta, the scan is often extended to the level of the aortic bifurcation for more complete assessment. Intravenous contrast administration may be followed with a saline bolus (30 mL normal saline) using a flow rate of 3 to 4 cc per sec for optimal enhancement. A saline bolus after contrast decreases the amount of streak artifact as it leads to rapid contrast washout within the superior vena cava, resulting in a more coherent bolus delivery. Delayed CT imaging is not usually performed for suspected acute aortic injury, but is routine for assessment after aortic surgery or endovascular repair.

In our institution, 2 mm to 4 mm slices are sent to the picture archiving and communications system (PACS) for interactive analysis. Additional left anterior oblique (LAO) 45-degree multiplanar reconstructions (MPR) are routinely created by the CT technologists and sent to PACS for review. These LAO MPRs are useful for demonstrating cranial-caudal extent of the aorta on 1 image. These images are created by placing the reconstruction plane parallel to the aortic arch resulting in the familiar "candy cane" view of the aorta (Figure 2).

Thinner (1 mm) reconstruction images are sent to a workstation for 3D reconstruction. Previously considered optional, reconstructions have become routine and are expected by the referring physicians for pretreatment planning. Semiautomated software is currently available that generates maximum and minimum bidimensional measurements of the aortic lumen in cross-section (Figure 3). Curved planar reconstructions (CPR), shaded surface display, maximum intensity projection (MIP), 2-dimensional oblique and 3-dimensional volumetric images are routinely created.

Aortic dissection

Acute thoracic aortic dissection is the most common cause of AAS. If undiagnosed and untreated, 38% of patients with aortic dissection will die by 24 hours with 50% mortality by 48 hours. Thus, it is important to rapidly and accurately identify aortic dissections. MDCT has displaced invasive aortography as the most widely used first-line diagnostic imaging modality; it is the most reliable, with sensitivity, specificity and accuracy approaching 100%. (4-7)

Dissection occurs when a laceration in the aortic intima allows pressurized blood to enter into and dissect between layers of the aortic media, forming a second or false lumen (as opposed to the true lumen). The points of greatest hydraulic stress in the aorta are the most common locations of intimal tearing: the right lateral aspect of the ascending aorta and the descending thoracic aorta proximal to the ligamentum arteriosum. (7) Systemic hypertension is the most frequent factor predisposing patients to aortic dissection. Other important etiologies for development of aortic dissection include de novo intramural hematoma with back rupture into the aortic lumen with subsequent blood flow into the media and cystic medial necrosis, as seen with Marfan's disease. The most widely used classification system for dissection is the Stanford classification: a dissection in the ascending aorta is considered type A and dissection in the descending aorta distal to the left subclavian artery origin is considered type B.

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Dissection is diagnosed on contrast-enhanced CT angiography (CTA), which allows visualization of both true and false channels, the intimomedial flap, and often, the intimal tear. In the aortic arch, the intimal tear is often best seen on the LAO 45-degree projection. The term intimal flap is a misnomer; the flap is composed of both media and intima, therefore the term intimomedial flap is preferred.

Pulsation artifact in the proximal ascending aorta can mimic a dissection flap. (4) The use of ECG gating can reduce or eliminate this potential false-positive finding although there is a tradeoff with radiation exposure (Figure 4). Clues to pulsation artifact include multiple, peripheral, curvilinear low-attenuation densities within the aorta as well as duplicated margins within adjacent cardiac chambers. With newer technology and subsecond scanning, this pitfall is less prevalent. ECG gating for aortic CTA can be used in cases of Marfan's syndrome or other connective-tissue disorders which have a higher incidence of proximal dissection involving the aortic cusps or the sinotubular junction. In addition, ECG gating allows for more accurate measurement of the aorta. Other potential abnormalities mimicking aortic dissection on axial images include coarctation, pseudocoarctation, saccular aneurysm and pseudoaneursym. MPRs will usually clarify the finding and lead to the correct diagnosis (Figure 5).

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Differentiation of the true from the false lumen is crucial for planning possible endovascular intervention. The true lumen is contiguous with the nondissected portion of the aorta and is usually smaller and more opacified than the true lumen during the angiographic phase of imaging. (6) The false lumen is often located between the 9:00 and 12:00 positions along the aortic lumen circumference of the ascending aorta and between the 3:00 and 6:00 positions in the descending aorta. (8) Although these features are helpful to distinguish between true and false lumens, they are not reliable. The most reliable sign to identify the true lumen is the presence of calcification in the periphery of the aorta (in the nonintimal flap side). The false lumen may be partially thrombosed demonstrating both slow flow and thrombus (9) (Figure 6). Other signs of the false lumen include the cobweb sign, which are linear densities within the opacified false lumen due to incompletely detached threads of aortic media, and the beak sign, which is when an angle is formed by the intersection of the intimomedial flap and outer wall of the false lumen. (6) A true lumen that is completely collapsed should not be mistaken for eccentric thrombus (8) (Figures 7 and 8).

An uncommon variant of dissection is intimointimal intussusception, in which a near 360-degree circumferential tear leads to central displacement of the intimal-medial flap. The etiology is usually a Stanford type A lesion in the aortic arch. In this case, the central lumen is invariably the true lumen. (7) Obstruction of the great vessels is a potential complication9 (Figure 9).

The complications of aortic dissection include: aneurysm formation, rupture, continuation of the dissection into the pericardium with or without tamponade, and extension into the carotid or coronary arteries causing stroke or myocardial infarction, respectively (Figure 6). Renal and mesenteric ischemia may occur from hypoperfusion due to dissection extension into branch vessels or branch-vessel perfusion via a less perfused true or false lumen. Dynamic occlusion can lead to end-organ ischemia if the intimal flap spares the branch vessel but repetitively prolapses and intermittently occludes its orifice. (6) A rare complication of a Type A dissection is rupture into the mediastinum. When this occurs, the mediastinal hematoma can dissect into the shared adventitia surrounding the pulmonary arteries and cause marked compressional narrowing (Figure 10).

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Intramural hematoma

Intramural hematoma (IMH) may be considered a variant of aortic dissection. It is the result of hemorrhage within the media from rupture of the vasa vasorum in the absence of an intimomedial tear in the setting of hypertension or trauma. Hypertension plays a major role in the pathogenesis of injury to the media. It contributes to spontaneous rupture of the vasa vasorum and mechanical strain on the aortic wall, both of which may lead to an intimal tear. IMH may also be caused by focal penetrating ulceration in an atherosclerotic plaque or thrombosed dissection lumen (Figure 11).

Clinically, IMH and dissection cannot be differentiated. As a result, all scans to exclude an aortic dissection should include precontrast imaging to evaluate for possible IMH. In the acute presentation on MDCT, there is a relatively circumferential crescent or ring-like hyperdensity along the margin of the aorta, mimicking a "thickened aortic wall." The high attenuation is best appreciated on precontrast imaging. There is no evidence of flow within the abnormality. Intramural hematomas do not enhance following intravenous contrast administration. Differential diagnosis for intramural hematoma includes entities that cause aortic-wall thickening such as aortitis, mural (intraluminal) thrombus and soft atheromatous plaque.

The management of IMH is similar to that of aortic dissection Type A and B. Intramural hematoma caused by a penetrating ulceration may progress to pseudoaneursym formation, requiring close monitoring.(9)

Acute IMH may be a precursor to fusiform aneurysm, dissection or pseudoaneursym. Approximately 2% to 20% of IMH results in acute aortic dissections as a consequence of penetrating ulceration. One proposed mechanism for the development of dissection from a preexisting IMH involves aortic branch artery pseudoaneurysms. These lesions mimic penetrating ulcerations and associated IMH, but they actually represent focal, mural pseudoaneursyms. Shearing injury is caused by the propogation of hematoma across the origin of the branch vessel; the origin of the intercostal or bronchial artery is thus "interrupted" resulting in a focal, high-attenuation, rounded focus, which is contiguous with the extra-aortic tubular course of the vessel (Figure 12). Because of the mechanism of injury, these pseudoaneursyms do not appear along the pleural surface of the aorta, which distinguishes them from penetrating ulcerations (10) (Figure 13).

Approximately 10% of IMH will regress (Figure 14), but progression is seen in 20% to 45% of patients. (2) Subacute or resolving IMH becomes isodense to blood on precontrast CT and slowly decreases in size.

Penetrating atherosclerotic ulcer

Penetrating atherosclerotic ulcer (PAU) is defined as an atherosclerotic lesion with ulceration that erodes the internal elastic lamina of the aorta and penetrates into the media. (11) The media is then exposed to pulsatile arterial flow, which leads to hemorrhage into the wall with IMH formation (Figure 15). (3) The IMH is usually localized due to fibrotic changes within the media caused by atherosclerosis, but it may occasionally be extensive. (4)

The typical presentation of PAU is in an elderly patient with hypertension and atherosclerosis, who complains of back or chest pain with a paucity of specific clinical signs; in particular, there is no pulse deficit and no evidence of aortic regurgitation, stroke or visceral-vessel compromise that would suggest a classical dissection. (11,12) Patients with PAU are usually older than patients with IMH or dissection and tend to present with advanced atherosclerotic disease. (7)

PAU can occur within the ascending or descending thoracic aorta. The true incidence of this disease is still unknown. Due to the high frequency of comorbid conditions, most authors advocate that patients with PAU be managed with close clinical monitoring, (13) unless persistent chest pain or development of complications warrants surgical treatment. The high surgical mortality has attracted attention to minimally invasive endovascular repair with stent grafts, but the impact on long-term prognosis is still unknown. (14)

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It is important to distinguish PAU from common atheromatous ulcers of the aorta. Atheromatous ulcers are usually small, confined to the intima and do not cause symptoms, although these lesions may eventually progress to PAU (Figure 15). On CT imaging, ulcerating atheromatous plaques without penetration through the intima will demonstrate irregular margins within the contrast-filled lumen without contrast material extension beyond the intima and no IMH. (3)

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PAU, in contrast, will present as a focal collection of contrast material that extends beyond the aortic intima and therefore is seen outside the aortic lumen, usually surrounded by an IMH of variable extent, which has a smooth interface with the contrast in the lumen. (3,7,8) Unenhanced CT images may demonstrate hyperdense IMH and displacement of intimal calcifications. (7,9)

PAU may be complicated by the development of true aneurysms, pseudoaneurysms (Figure 15), dissection and aortic rupture (Figure 16)4. As opposed to true aneurysms, pseudoaneursyms do not contain all 3 layers of the aortic wall, are saccular in shape and may be comprised of solely adventitia, enclosing a hematoma. The risk of aortic rupture is believed to be higher for PAU than for IMH or aortic dissection.15 When PAU results in aortic rupture with mediastinal hemorrhage, it may be difficult to differentiate it from a ruptured aneurysm, but in both cases, immediate surgery is necessary. (7)

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Unstable aortic aneurysm

Unstable aortic aneurysms include aneurysms that enlarge rapidly, show signs of imminent rupture or have already ruptured. (6) Aortic thoracic aneurysm, by definition, is a permanent localized dilatation, usually fusiform, [greater than or equal to] 50% of normal or >5 cm and involving all 3 layers of the aortic wall. (6,16)

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The mechanism of aortic leak and rupture involves the presence of areas of high- and low-wall stress within the aneurysm related to blood pressure. The increased stress results in dilatation of the aneurysm. This expansion subjects the wall to even greater tension, which causes more dilatation, until the mechanical stress on the wall exceeds its strength, leading to rupture. (17) Mycotic aneurysms have a marked tendency to rupture. In addition, there is a risk of uncontrolled sepsis, which gives this disease a high mortality rate.9,17

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Clinical presentation includes chest or back pain similar to other causes of acute aortic syndrome, but these patients are usually not hypertensive.

CT signs of imminent contained rupture include hyperdense thickening of the aortic wall ("crescent sign") representing IMH, discontinuous calcification in a circumferentially calcified aorta ("missing calcium sign"), eccentric nipple shape to the aorta, and an aorta that conforms to the neighboring vertebral body ("draped aorta"). (2,6) The risk of rupture is proportional to the size of the aneurysm and the rate of expansion. (9)

CT signs of rupture include mediastinal hematoma (Figure 17), stranding of the periaortic fat, hemothorax (usually left-sided), and more rarely pericardial effusion. (2,6) CT may also show evidence of hypovolemic shock, including reduction of the diameter of the central vessels, particularly the inferior vena cava, and excessive enhancement of the aorta. (2)

Conclusion

As delineated above, penetrating ulceration, intramural hematoma and aortic dissection are inter-related, may coexist, and have a causal relationship. Although each may occur spontaneously, penetrating ulceration may lead to either or both IMH and aortic dissection. Spontaneous IMH may lead to dissection. The thrombosed false lumen of a classic aortic dissection represents IMH. These diseases are not static and may progress with time. PAU, as well as dissection, may lead to pseudoaneursym formation, which may necessitate repair. Both true aneurysms and pseudoaneursyms may lead to aortic rupture. CT plays an important role in the diagnosis of acute aortic syndromes.

References

(1.) Vilacosta I, San Ramon JA. Acute aortic syndrome. Heart, 2001;85:265-268.

(2.) Salvolini L, Renda P, Fiore D, et al. Acute aortic syndromes: Role of multi-detector row CT. Eur J Radio. 2008;65:350-358.

(3.) Macura KJ, Corl FM, Fishman EK, et al. Pathogenesis in acute aortic syndromes: Aortic dissection, intramural hematoma, and penetrating atherosclerotic aortic ulcer. AJR Am J Roentgenol. 2003;181:309-316.

(4.) Manghat NE, Morgan-Hughes GJ, Roobottom CA. Multi-detector row computed tomography: Imaging in acute aortic syndrome. Clin Radiol. 2005;60:1256-1267.

(5.) Chughtai A, Kazerooni EA. CT and MRI of acute thoracic cardiovascular emergencies. Crit Care Clin. 2007;23:835-853, vii.

(6.) Smith AD, Schoenhagen P. CT imaging for acute aortic syndrome. Cleve Clin J Med. 2008:75: 7-9,12,15-17 passim.

(7.) Castaner E, Andreu M, Gallardo X, et al. CT in nontraumatic acute thoracic aortic disease: Typical and atypical features and complications. Radiographics. 2003;23:S93-110.

(8.) Bhalla S, West OC. CT of nontraumatic thoracic aortic emergencies. Semin Ultrasound CT MR. 2005;26:281-304.

(9.) Macura KJ, Szarf G, Fishman EK, et al. Role of computed tomography and magnetic resonance imaging in assessment of acute aortic syndromes. Semin Ultrasound CT MR. 2003;24:232-254.

(10.) Williams DM, Cronin P, Dasika N, et al. Aortic branch artery pseudoaneurysms accompanying aortic dissection. Part I: Pseudoaneurysm anatomy. J Vasc Interv Radiol. 2006;17:765-771.

(11.) Stanson AW, Kazmier FJ, Hollier LH, et al. Penetrating atherosclerotic ulcers of the thoracic aorta: Natural history and clinicopathologic correlations. Ann Vasc Surg. 1986;1:15-23.

(12.) Singhal P, Lin Z. Penetrating atheromatous ulcer of ascending aorta: A case report and review of literature. Heart Lung Circ. 2008;17:380-382.

(13.) Cho KR, Stanson AW, Potter DD, et al. Penetrating atherosclerotic ulcer of the descending thoracic aorta and arch. J Thorac Cardiovasc Surg. 2004;127:1393-1399; discussion 1399-1401.

(14.) Gottardi R, Zimpfer D, Funovics, et al. Midterm results after endovascular stent-graft placement due to penetrating atherosclerotic ulcers of the thoracic aorta. Eur J Cardiothorac Surg. 2008; 33:1019-1024.

(15.) Coady MA, Rizzo JA, Elefteriades JA. Pathologic variants of thoracic aortic dissections: Penetrating atherosclerotic ulcers and intramural hematomas. Cardiol Clin. 1999;17:637-657.

(16.) Mitchell RS, Dake MD, Sembra CP, et al. Endovascular stent-graft repair of thoracic aortic aneurysms. J Thorac Cardiovasc Surg. 1996; 111:1054-1062.

(17.) Macura KJ, Corl FM, Fishman EK, et al. Pathogenesis in acute aortic syndromes: Aortic aneurysm leak and rupture and traumatic aortic transection. AJR Am J Roentgenol. 2003;181: 303-307.

Maria C. Shiau, MD, Myrna C. B. Godoy, MD, Patricia M. de Groot, MD, and Jane P. Ko, MD

Dr. Shiau, is an Assistant Professor of Radiology, and Dr. Ko is an Associate Professor of Radiology, Department of Radiology, New York University Langone Medical Center, Department of Radiology, New York, NY; Dr. de Groot is an Assistant Professor of Radiology, Department of Radiology, Virginia Commonwealth University Health System, Richmond, VA; and Dr. Godoy is an Assistant Professor of Radiology, Department of Diagnostic Radiology, The University of Texas M.D. Anderson Cancer Center, Houston, TX.
Table 1. Aortic CT imaging protocol.

Phase 1: Precontrast
                            4-slice     16-slice

  Detector configuration    4 x 2.5     16 x 1.5
  Rotation time             0.5 sec     0.4 sec
  kVp                       120         120
  mAs/effective mAs **      150         150
  Reference effective mAs   N/A         150
  Mm/rotation               Pitch 0.8   Pitch 0.8
  Coverage                  2 mm above aorta to renal arteries
  PACS reconstructions      4 q 4       4 q 4
  Recon algorithm           Low frequency: Soft-tissue windows (B40
                              Siemens, FC01Toshiba, Standard GE)
  Field of view             Smallest possible (maximum spatial
                              resolution)

Phase 2: Postcontrast
                            4-slice     16-slice

  Detector configuration    4 x 2.5     16 x 0.75
  Rotation time             0.5 sec     0.4 sec
  kVp                       120         120
  mAs/effective mAs **      150         150
  Reference effective mAs   N/A         150
  Mm/rotation               Pitch 0.8   Pitch 0.8
  Coverage                  Apices to renal arteries for aneurysm;
                              apices to iliac bifurcation for
                              dissection
  PACS reconstructions      2 q 2, 5 q 52 q 2
  Recon algorithm           Low frequency: Soft-tissue windows (B40
                              Siemens, FC01Toshiba, Standard GE)
  Field of view             Smallest possible (maximum spatial
                              resolution)
  IV contrast: volume       120 cc nonionic contrast at 3 cc/sec
    and rate
  Scan delay                Bolus tracking (130 HU)

Phase 1: Precontrast
                            64-slice      128-slice

  Detector configuration    64 x 1.2      64 x 1.2
  Rotation time             0.4 sec       0.33 sec
  kVp                       120           120
  mAs/effective mAs **      150           150
  Reference effective mAs   150           150
  Mm/rotation               Pitch 0.8 *   Pitch 0.8
  Coverage
  PACS reconstructions      4 q 4         4 q 4

  Recon algorithm

  Field of view

Phase 2: Postcontrast
                            64-slice      128-slice

  Detector configuration    32 x 0.6      64 x 0.6
  Rotation time             0.33 sec      0.33 sec
  kVp                       120           120
  mAs/effective mAs **      150           150
  Reference effective mAs   150           150
  Mm/rotation               Pitch 0.8 *   Pitch 0.8
  Coverage

  PACS reconstructions      2 q 2         2 q 2
  Recon algorithm

  Field of view

  IV contrast: volume
    and rate
  Scan delay

* 64-slice GE requires pitch of 1.3

** Effective mAs for Siemens scanners
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