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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3734_Библиотеки_им_академика_М_И_Перельмана

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Imaging ofAortic Dissection: CT, MRI, andAngiography
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Fig. 6 (a) ECG demonstrating an inferoposterior ST elevation myocardial infarction in a patient presenting with chest pain. (b) Invasive aortography was performed following activation of the cardiac catheterization lab for an ST elevation myocardial infarction and non-obstructive coronary angiography. In this case, aortography demonstrated a double lumen with an intimal ap (arrow) and differential opacication of the two lumens within the ascending aorta. (c) ECG-gated CT angiography of the chest (shown), abdomen, and pelvis was subsequently performed to conrm the diagnosis and evaluate the extent of the dissection. An intimal ap is present in the aortic root extending into the ostium of the right coronary artery
presence of a hyperattenuating (>40HU) uid collection within the pericardium, pleural space, or mediastinum is suggestive of aortic rupture on both non-contrast and contrast studies (Figs.7 and 8) [4]. With contrast administration, irregularity of the aortic wall may be noted, or frank extravasation of vascular contrast into the uid collection [20].
The identication of features suggestive of a complicated dissection with end­organ malperfusion or evidence of rupture is of almost equal importance to diagnos­ing the presence of an aortic dissection. In up to 30% of patients with an aortic
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Fig. 7 ECG-gated CT angiography of the chest with a large hyperattenuating (~54 Hounseld units) pericardial effusion (asterisk), concerning for hemopericardium and aortic rupture in the setting of a Type A aortic dissection
Fig. 8 ECG-gated CT angiography of the chest with a large hyperattenuating (~62 Hounseld units) mediastinal uid collection (asterisk) compressing the main pulmonary artery (arrow), concerning for mediastinal blood products due to aortic rupture in the setting of a Type A aortic dissection
A. Tower-Rader et al.
dissection, and approximately 10% of patients with a type B aortic dissection, evi­dence of end-organ malperfusion is apparent at the time of initial presentation [2, 5]. While the most common description is of the celiac trunk, superior mesenteric and right renal arteries arising from the true lumen, and the left renal artery arising from the false lumen, signicant variation has been noted in the pattern of abdominal branch vessel involvement [15]. It is important to examine whether each branch, including the head and neck vessels, arises from the true or false lumen, as well as the presence and mechanism of end-organ malperfusion for each branch vessel ter­ritory. End-organ malperfusion may be due to one of four mechanisms: (1) static occlusion of the branch artery by extension of the dissection ap into the ostium or proximal segment, (2) dynamic due to the dissection ap prolapsing over and inter­mittently occluding the ostium of the non-dissected branch vessel, (3) mixed static and dynamic, or (4) ostial disconnection and avulsion from the true lumen [10, 14,
21]. The mechanism of occlusion is important to identify since it inuences
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management: static occlusion is often treated with a stent, whereas dynamic occlu­sion may be managed by creating fenestrations in the intimal ap to reduce the pressure within the false lumen [10, 14]. Additionally, the evaluation of the ostia and proximal segment of each branch vessel of the aorta is crucial to understanding which organs may be at risk for ischemia. Regardless, careful inspection of the abdominal organs for evidence of decreased perfusion should also be performed (Fig.9). Delayed phase imaging may be helpful in differentiating complete versus delayed perfusion of a vascular territory in the setting of a chronic dissection; how­ever, in the setting of acute symptoms, organ hypoperfusion on arterial phase imag­ing is presumed to represent an area at risk and delayed phase imaging is typically not included in the protocol in order to decrease both the acquisition time and radia­tion dose of the study. Reports should include a detailed description of whether the aortic branch vessels are involved in the dissection, patency of the ostia and proxi­mal aortic branch vessels, and evidence of decreased organ perfusion or infarction (Table2).
Additional Findings onCT Imaging
In addition to obtaining data regarding the aorta itself, additional information is obtained regarding both cardiovascular and non-cardiovascular structures, which may give clues to an underlying syndrome or predisposition for aortic dissection, alternative diagnosis, or mayhelp guide surgical planning. As is discussed in depth in the sections regarding long-term imaging of the aorta and management of chronic
Fig. 9 CT angiography of the abdomen demonstrating an aortic dissection with the left renal artery arising from the true lumen and an intimal ap extending to the ostium of the right renal artery, resulting in occlusion by the false lumen (arrow). Additionally there is hypoperfusion of the right kidney (asterisk), which is readily apparent, especially in comparison to the well-perfused left kidney
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dissections, several imaging features have been identied that are predictive of future aortic dilation and adverse aortic events (Table 3). With the use of ECG­gating MDCT, it is possible to identify the aortic valve as well as the anatomy of the sinotubular junction. The identication of a bicuspid aortic valve carries additional implications for follow-up for the patient, as well as rst degree relatives. In the case of syndromic connective tissue disorders, including Marfan, vascular type Ehlers­Danlos and Loeys-Dietz syndromes, additional associated features may be identi­ed including pectus deformity of the chest wall, scoliosis or kyphosis, dural ectasia, or lung bullae. One of the other main benets of MDCT in comparison to other imaging modalities is that in the absence of an aortic dissection other etiologies of chest pain may be identied, including pulmonary embolus, pneumothorax, orpul­monary or chest wall mass. In patients who have undergone prior sternotomy it is important to detail the proximity of cardiovascular structures to the sternum, par­ticularly bypass grafts and whether they cross the midline, since this may affect planning for a redo sternotomy. Reports should include information regarding prox­imity of cardiovascular structures to the sternum, as well as featuresthat may sug­gest an underlying syndrome since the management of these patients in the acute and chronic phases, and the implications for screening of family members varies (Table2).
Magnetic Resonance Imaging
Magnetic resonance imaging (MRI) is best reserved for stable patients, or those with chronic dissections. Prior studies have demonstrated a sensitivity and specic­ity of 95–98% and 94–98%, respectively, for the detection of an aortic dissection [9]. Several different types of MRI sequences are available for imaging the aorta including cine (dynamic) imaging, MR angiography, and respiratory navigator­gated 3D acquisitions. In addition to assessment of the aorta, cine MRI imaging allows for the assessment of aortic regurgitation, left ventricular function, and peri­cardial effusions, offering the potential to obtain additional data regarding cardiac function and potential complications of a type A dissection as part of the study.
Table 3 Imaging features predictive of aortic dilation and adverse aortic events
• Partially thrombosed false lumen>patent false lumen>thrombosed false lumen
• Maximal aortic diameter40mm
• Fusiform index0.64
• False lumen diameter22mm in the proximal descending aorta
• Crescent shape of the true lumen
• Thrombosed false lumen with ulcer-like projections (especially in the proximal descending aorta)
• Entry tear10mm in the proximal descending aorta
Fusiform index=Maximum diameter of descending aorta/(diameter of the distal aortic arch+diam­eter of the descending aorta at the level of the pulmonary artery)
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Unfortunately, despite these benets, the relatively long acquisition time (approxi­mately 20–30min), as well as the inability to adequately monitor patients who are potentially hemodynamically unstable, makes the use of MRI for diagnosing an acute dissection far less appealing [3]. However, MRI may be used in select sce­narios where an acute aortic dissection is suspected, for instance in a hemodynami­cally stable patient with a severe allergy to iodinated contrast, or in a facilitythat does not have immediate access to transesophageal echocardiography. Instead, MRI is often used for monitoring patients with a chronic dissection due to the lack of radiation exposure, and, with newer techniques, the ability to avoid contrast admin­istration altogether. MR angiography is also ill-suited for patients with advanced renal dysfunction and pregnancy since gadolinium chelate contrast agents are con­traindicated. Implantable medical devices may be problematic either because the device is not MRI compatible, or due to artifacts created by the device interfering with image interpretation.
MRI Findings
As with CT, a dissection is often identied on MRI with the presence of a double­barrel lumen on axial images. In particular, spin-echo black-blood sequences allow for the rapid identication of an intimal ap [22] (Fig.10). The true lumen can be identied using the same anatomic considerations as with MDCT; the true lumen is usually smaller and in continuity with the unaffected aorta. Thrombus within the false lumen is hypointense on T1 and T2 imaging [22]. Again, the status of all of the aortic arch and abdominal aortic branches should be described. Pericardial and pleural effusions may be recognized by their high signal intensity on axial imaging. ECG-gated gradient echo sequences can be displayed as cine images with areas of
Fig. 10 Magnetic resonance imaging with spin-echo black blood imaging demonstrating an intimal ap (arrow) with partial thrombosis of the false lumen (asterisk)
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turbulent ow creating dephasing andresulting in a signal void, which may be use­ful in identifying aortic regurgitation or ow between the true and false lumens. MR angiography utilizes 3D spoiled gradient echo sequences and a gadolinium-chelate contrast agent and is rapidly acquired during a single breath-hold with high- intensity signal localized to the intravascular space (Fig.11). Typically unenhanced, arterial and delayed phase images are obtained. MR angiography results in the reconstruc­tion of a 3D dataset, which may then be manipulated to allow for multiplanar recon­struction of cross-sectional sections to the lumen to measure aortic dimensions in a similar fashion to CT [11]. Non-contrast techniques for acquisition and reconstruc­tion of a 3D dataset, including respiratory navigator-gated, ECG-gated 3D whole heart balanced steady state free precession, have a long acquisition time (10–12min) and are thus ill-suited for imaging in the acute setting [23].
Angiography
Prior to the advent of non-invasive techniques for evaluating the aorta, aortography was considered the standard for diagnosis for an aortic dissection. As a primary diagnostic tool angiography has fallen out of favor compared to other modalities because it is invasive, time-consuming, requires an experienced operator, and exposes the patient to both iodinated contrast and radiation. Digital subtraction angiography (DSA) is still utilized in a few clinical scenarios and thus, it is still important to understand the appearance of a dissection on DSA, as well as the dis­advantages of the technique. For instance, DSA is often utilized during endovascu­lar treatment of a dissection, and may be useful as a diagnostic tool for patients presenting to the cardiac catheterization lab for chest pain with a suspected acute coronary syndrome who are found to have non-obstructive coronary arteries and an alternative diagnosis of aortic dissection is suspected. Aortography may also be
Fig. 11 Magnetic resonance imaging with contrast enhanced angiography, revealing an intimal ap (arrow) and double barrel lumen in the abdominal aorta
Imaging ofAortic Dissection: CT, MRI, andAngiography
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necessary to diagnose an aortic dissection for institutions without access to nonin­vasive imaging (MDCT or MRI) or transesophageal echocardiography. Aortography involves the placement of a pigtail catheter placed within the aortic lumen, with injection of iodinated contrast initially by hand to conrm catheter placement fol­lowed by injection via a hydraulic power injector with digital subtraction cine uo­roscopic imaging [24]. Initially aortography was thought to be associated with a risk for propagation of the dissection, but further study demonstrated the procedure to be relatively safe, thus becoming the standard for diagnosis around 1970 [25]. The sensitivity and specicity of angiography are also lower than with MDCT and MRI at 88% and 94%, respectively [26].
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Angiography Findings
Following injection of iodinated contrast within the aorta lumen, the lumen of the aorta, as well as its branches, become opacied. The presence of double lumen with an intimal ap and communication between the two lumens is diagnostic for an aortic dissection [24] (Fig.6a–c). Either ow reversal or stasis of contrast within the false lumen is often seen. Indirect signs of an aortic dissection include compression of the true lumen, thickening of the aortic wall, out-pouchings along the aortic wall, failure of aortic branches to ll, and aortic regurgitation [24, 2628]. Injection of contrast alters the pressure dynamics between the true and false lumen and thus the assessment of malperfusion syndromes proves more complicated. False positives may occur when the true and false lumens opacify simultaneously [29]. Additionally, angiography is not capable of identifying intramural hematoma or patients with a completely thrombosed false lumen, especially if there is no aortic branch vessel involvement [27].
Conclusions
In conclusion, the sensitivity and specicity of MDCT and MRI for the detection of an aortic dissection are similar [9], though the relative length of MRI and inability to fully monitor patients hemodynamically make it less ideal for the evaluation of an acute aortic dissection unless the patient is stable and unable to receive iodinated contrast. Angiography, previously the standard for diagnosis, is less sensitive and specic for aortic dissection, though it does still play a role during endovascular procedures, or for further evaluation of patients with chest pain who are already in the cardiac catheterization laboratory for assessment of chest pain. Choice of imag­ing modality is inuenced by institutional accessibility and expertise, though the advantages and disadvantages of each modality should be recognized by providers.
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Imaging ofIntramural Hematoma
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andPenetrating Atherosclerotic Ulcer byCT andMRI
ZacharyHartley-Blossom, SaurabhAgarwal, andMichaelK.Atalay
Introduction
Intramural hematomas (IMH) and penetrating atherosclerotic (or aortic) ulcers (PAU) are two lesions on the spectrum of acute aortic syndromes (AAS), and their timely, accurate diagnosis is paramount for appropriate triage and management. Among all AAS, IMH constitutes ~4–11% of cases in North American and European populations and~28–32% of cases in Asian populations—highlighting geographic differences—while PAU accounts for less than 10% of such injuries [15]. Aortic dissection remains the leading cause of AAS, accounting for 65–75% of all cases [47], and is discussed in another chapter.
Imaging is essential for the prompt diagnosis of IMH and PAU. This chapter aims to describe the imaging protocols, lesion characteristics, and diagnostic challenges regarding both IMH and PAU, specically focusing on computed tomography (CT) and magnetic resonance imaging (MRI). These two cross­sectional imaging modalities provide complementary approaches to the diagnosis and management of AAS including the identication of associated ndings and complications. CT is generally preferred in the acute setting due to its high accuracy, ease of use, speed, and ready-access in most emergency departments.
This chapter will: (1) briey review normal aortic anatomy, (2) discuss the basic pathophysiology of IMH and PAU, (3) describe pertinent MRI and CT techniques and the salient imaging ndings of PAU and IMH—along with potentially useful prognostic features and diagnostic pitfalls—and nally (4) briey mention management options that are covered in greater detail elsewhere.
Z. Hartley-Blossom · S. Agarwal · M. K. Atalay (*) Department of Diagnostic Imaging, Rhode Island Hospital, Warren Alpert School of Medicine of Brown University, Providence, RI, USA
J. S. Coselli et al. (eds.), Aortic Dissection and Acute Aortic Syndromes,
https://doi.org/10.1007/978-3-030-66668-2_11
149© Springer Nature Switzerland AG 2021