Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:
Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1056_Библиотеки_им_академика_М_И_Перельмана.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
23 Мб
Скачать
11 Magnetic Resonance and Traditional Radiology in the Diagnosis of... 169
patients usually suffer from perineal pain, fever, and leukocytosis (Khati et al. 2015; Guniganti et al. 2017). The advantages of CT include its high availability, relatively low cost, rapid execution, great patient tolerance, and excellent spatial resolution. It can precisely reveal even small amounts of free air, presence of calcications, and internal bleeding (Guniganti et al. 2017).
The most appropriate CT protocol varies, depending upon patient presentation and differential diagnosis (Guniganti et al. 2017). Rectal contrast (gastrogranor barium) is not always required, and it is usually administered through a well­lubricated small rubber catheter gently inserted up the anal canal into the rectum prior to scanning (Khati et al. 2015). This catheter, left in place during scanning, may help to differentiate the anal canal from any potential stula and abscess.
Reformatted sagittal and coronal images are also obtained if needed. The creation of multiplanar reconstructions in CT provides a better recognition and characteriza­tion of anorectal pathology, and they are extremely useful in order to evaluate the supra-levator extension of disease (Guniganti et al. 2017).
Administration of intravenous contrast is much preferred to non-contrast exam­ination, as it helps to detect smal l uid collections and presence of inammation and to better delineate the anatomic relationship among perianal structures (Guniganti et al. 2017) (Fig. 1).
Using CT technique, a stulous tract appears as a well-dened tubular, soft tissue, or uid/air-lled structure that arises from the anal sphincter (Fig. 2). A thick, enhanced wall along with surrounding inammatory changes usual ly refers to an infected stula (Khati et al. 2015; Guniganti et al. 2017). An abscess is identied as a uid collection surrounded by a thick wall that may contain some air, and sometimes it is associated with a stulous tract (Khati et al. 2015; Guniganti et al. 2017). Surrounding inammatory changes among perianal structures are usually present (Khati et al. 2015).
Fig. 1 (a) Axial and (b) coronal CT images show the anatomy of the perianal region. AC anal canal, IS internal sphincter, ES external sphincter, IAF ischiatic-anal fossa, IRF ischiorectal fossa, SS supra-levator space, R rectum, LAM levator ani muscle
170 L. M. Minordi et al.
Fig. 2 Contrast-enhanced axial CT image shows a complex stula with an internal opening in the anterior midline and bilateral inter-sphincteric extensions (white arrows) into the anterolateral direction, with a horseshoe conguration
CT stulography is performed after the injection of contrast medium into the stula (Liang et al. 2014; Soker et al. 2016).
In the study performed by Liang et al. in 2014 (Liang et al. 2014), the patients were placed in a prone position. Before performing the scan, an enema tip was inserted into the rectum to the near maximum patient tolerance, and it was used to insufate air in order to discover the internal stula opening. Adequate intestinal distension is crucial for a correct visualization of the internal opening. CT scan views allowed a vigilant monitoring of the insufation, gradually performed, in order to avoid the risk of perforation. An infusion tube with the needle removed was cut in at the site of the external opening under rigorous disinfection measures. The tip of the infusion tube was dipped in xylocaine gel for a local anesthetic effect and lubrica­tion. The site of the external opening was cleaned well with alcohol and a povidone­iodine solution. The infusion tube was cleaned thoroughly using a compatible enzymatic detergent. A prepared solution (1 mL gastr ogran mixed in 10 mL of sterile normal saline) was gradually injected into the stula. Different volumes of the contrast mixture were utilized depending on the branching, width, and length of the perianal stula. Reow of contrast from the external opening indicated that the appropriate amount of contrast had been injected. At that point the external opening was closed with sterile gauze, and any contrast reuxed on the skins surface was cleaned off. Then, the contrast was injected through all openings to completely ll the perianal stula. The images were reconstructed on a workstation, including techniques such as maximum intensity projection, volume rendering (VR), and multiple planar reconstructions. The authors concluded that stulography improved the diagnostic effectiveness in the assessment of the stulous course.
In the study performed by Soker et al. in 2016 (Soker et al. 2016), stulography CT exams were evaluated in comparison with MRI and surgical reports. In CT the
11 Magnetic Resonance and Traditional Radiology in the Diagnosis of... 171
location of the external orice was found on the prone position of the patient, and the region was cleaned with alcohol and povidone-iodine solution. Then, a mixture of 1 mL of nonionic iodinated contrast material and 10 mL of saline was injected without a needle into the orice, following an application of xylocaine gel to anesthetize the local area. Intravenous iodinated contrast media was injected in all patients. Axial and three-dimensional (3D) recons tructed images of all patients were evaluated on a separate workstation. CT stulography allowed an exact evaluation of the stula classication in 30 (73.1%) of the 41 patients; on the other hand, MRI correctly dened stula classication in 38 (92.7%) of these patients. CT stulography revealed 29 secondary extensions in 16 patients, whereas MRI revealed 28 secondary extensions in 15 patients. There were no major discordances between surgical ndings and these two modalities. Comparing the ability to localize internal openings, CT stulography was able to detect the locations in 28 patients (68.2%), whereas MRI was more accurate in this aspect, allowing a correct evalu­ation in 35 patients (85.3%).
CT stulography is a technique with many disadvantages: it is an invasive, not well-tolerated, and time-consuming procedure. It carries risks associated with an inappropriate injection, and it may cause tissue injuries and false passages and fail to demonstrate details of the stulous tract. Other complications associated with this procedure include infection, sepsis, and aggravation of pain (Soker et al. 2016). Other relevant drawbacks of CT compared to MRI are its lower soft tissue contrast resolution and exposure to ionizing radiation (Guniganti et al. 2017). The superior soft tissue contrast resolution of MRI makes it a superior imaging technique in most clinical scenarios, allowing an accurate diagnosis, depicting perianal stulae and their relationship to the anal sphincter, and revealing stulas between pelvic organs, especially in patients with cryptogenic stulas or abscesses (Guniganti et al. 2017).
2.3 Magnetic Resonance Imaging
Over the past two decades , MR imaging has gained a prominent role in the management of patients with anal stulas. This is due to the fact that MRI can classify stulas preoperatively with very high precision. Many studies have demon­strated the remarkable diagnostic value of MRI, showing high accuracy of up to 93% (Beets-Tan et al. 2001; Halligan 2020). The favora ble results of these studies conrm that MRI is presently the method of choice for the assessment of perianal stulas and associated complications due to its high soft tissue contrast and the multiplanar capability (Vanbeckevoort et al. 2014; Baskan et al. 2014; Balcı et al. 2019; Vo et al.
2019).
2.3.1 Anatomy MRI
On phased-array 1-3-T MRI, the mean length of the anal canal is 4.4 cm measured from the anorectal junction to the most caudal extent of the subcutaneous external anal sphincter (Erden et al. 2017) (Fig. 3).
172 L. M. Minordi et al.
Fig. 3 (a) Axial T2-weighted image, (b) axial contrast-enhanced fat-suppressed T1-weighted image, (c) coronal T2-weighted image, and (d) coronal contrast-enhanced fat-suppressed T1-weighted image show anatomy of the perianal region. AC anal canal, IS internal sphincter, ES external sphincter, IAF ischiatic-anal fossa, IRF ischiorectal fossa, SS supra-levator space, R rectum; LAM levator ani muscle
The dentate line is situated at approximately half of the length of the canal, which is usually at the middle point between the superior border of the puborectalis muscle and the most caudal tip of the subcutaneous external sphincter. These structures demarcate the surgical anal canal, different from the anatomic anal canal, which is shorter and dened as the canal caudal to the anal valves. The dentate line is generally not directly identiable at MRI. However, its placement can be estimated especially in coronal reconstructions, where the cranio-caudal extent of the puborectalis muscle and external sphincter can be more easily appreciated (Erden et al. 2017; Halligan 2020).
The wall of the anal canal is formed by roughly cylindrical-shaped layers: the mucosa, submucosa, and muscularis. The inner muscular layer forms the internal anal sphincter and the outer layer the external anal sphincter complex (Erden et al. 2017).
11 Magnetic Resonance and Traditional Radiology in the Diagnosis of... 173
The internal sphincter can be recognized as the thickened extension of the circular smooth muscle layer of the rectum, and it ends proximal to the lower part of the external anal sphincter. It is homogenous and moderately hyperintense on T2-weighted images and enhances signicantly after administration of contrast agent. On axial MR images, the internal anal sphincter is seen as an inner circular layer of the anal canal. It appears as a longitudinal band on the coronal plane. The mean thickness of the internal anal sphincter is about 3.5 mm, being approximately
3.2 0.7 mm in women and 2.9 0.7 mm in men. The thickness of the internal anal sphincter increases with age. This is most likely due to the inltration of connective tissue rather than genuine muscular hypertrophy (Erden et al. 2017).
The external sphincter complex is formed by skeletal muscle. On axial T2-weighted images, it can be recognized as an outermost circular layer of the anal canal. It has low signal intensity with striatedappearance. After administra­tion of intravenous contrast agent, the external anal sphincter appears less enhanced than the internal anal sphincter. It is thicker than the internal sphincter, with a mean value of about 4 mm. According to the traditional description, the external anal sphincter has three separa te muscular ber bundles: deep, supercial, and subcuta­neous. All these three components can be distinguished only on high-resolution T2-weighted images. The deep part of the external anal sphincter surrounds the upper third of the anal canal and joins proximally with the sling-like puborectalis muscle. The supercial part is the largest of the three layers, it strengthens the bulk of the internal anal sphincter on all sides and surrounds the anal canal above the subcutaneous external anal sphincter; it continues within the ano-coccygeal liga­ment, which adheres posteriorly to the coccyx. The subcutaneous part is an annular muscle, which circles the anal canal at the infero-lateral region of the internal anal sphincter, and is situated immediately under the perianal skin; the subcutaneous part of the external anal sphincter extends under the internal anal sphincter and curves medially with a typical J shape. On MRI, the mean thickness of the subcutaneous external anal sphincter on each side is about 5 mm in normal subjects (Erden et al.
2017).
In the space that separates the external and the internal anal sphincter, there is a bro-fatty muscular layer called conjoint longitudinal muscle (CLM). It continues superiorly with the longitudinal muscle layer of the rectum. On the axial T1- and T2­weighted MR sections, the CLM shows a thin hypointense circular conguration. It enhances after injection of intravenous contrast agent. It is a very thin layer with a mean thickness of 1.63 0.44 at histo-topographic study, and it varies between 0.9 and 1.6 mm on phased-array MRI (Erden et al. 2017).
The inter-sphincteric space is a potential space between the conjoint longitudinal muscle and the external anal sphincter. It shows as a thin hyperintense area on the axial T1- and T2- weighted images. Most perianal stulas originate from this space (Erden et al. 2017).
Puborectalis muscle is the part of the levator ani group of muscles, which emerges from the body of the pubic bone and forms a sling around the anorectal junction. This sling causes angulation of the rectum, partially contributing to continence. It typically has a shape of a U,which can be easily recognized on the axial plane. Its
174 L. M. Minordi et al.
mean thickness is 4.28 0.13 mm on phased-array MRI. The absence of puborectalis muscle weakens the anterior aspect of the canal (Erden et al. 2017).
The anorectal angle determines a fundamental parameter of the anorectal cong­uration. It is dened as the angle formed by the lines passing from the posterior wall of the rectum and through the center of the anal canal. The normal range of this angle can be quantied in MRI and measures, in asymptomatic subje cts at rest, between 93 and 108 (Erden et al. 2017).
Ano-coccygeal ligament (also called ano-coccygeal raphe) is a complex musculotendinous structure extending between the coccyx and anal canal. It is a crucial structure for decision-making regarding rectal and upper anal canal mobili­zation. Its mean diameter on the axial MR images is 7.28 0.17 mm (Erden et al.
2017).
2.3.2 MRI Technique (Coils, Volume, and Sequences) and Findings
Endoluminal anal coil and body phased-array coils can be used.
Since MRI eld strengths and phased-array coils have advanced their diagnostic performance, dedicated endoluminal anal coils are now infrequently utilized, although they provide the best spatial resolution. Other factors that led to this tendency are their restricted eld of view (which may not allow to visualize all the stulous tracts and abscesses outside the sphincter complex), low tolerance by patients, and frequent motion artifacts (Dwarkasing et al. 2005; George et al.
2011; Vanbeckevoort et al. 2014).
On the other hand, MRI exam performed with body phased-array coils does not need any particular patient preparation and is better tolerated. Advantages of the body phased-array coils include a larger eld of view (avoiding stula extensions from being overlooked) and a good spatial resolution (even though not as much as endoluminal coils) (George et al. 2011; Vanbeckevoort et al. 2014; Baskan et al.
2014).
The imaged volume should include all the frequent sites of the stula extensions: the levators, the whole presacral space, and the perineum (Baskan et al. 2014).
Another important advantage of MR imaging in stula evaluation is the capacity to study the anal sphincter complex in any surgically relevant plane. For this reason, it is crucial that imaging planes are correctly oriented with respect to the anal canal. The anal canal is leaned forward from the vertical by approximately 45
in the sagittal plane, making it necessary to obtain axial and coronal images aligned orthogonal and parallel to the anal canal, respectively. Normally oriented axial and coronal images would not allow precise analysis of the source and the stulous track (de Miguel Criado et al. 2012; Baskan et al. 2014). At rst the precise inclination of the anal canal is evaluated in a T2-weighted sequence in the sagittal plane in order to acquire these correctly orientated planes (de Miguel Criado et al. 2012; Baskan et al.
2014). This sequence provides the correct orientation of the anal canal, so that truly
axial (Fig. 4a) and coronal (Fig. 4b) images along the long axis of the anal canal can be obtained. Axial images frequently allow an accurate evaluation of the primary track (e.g., ischioanal or inter-sphincteric), and they are also ideal to show the radial site of the internal opening. Coronal images are excellent for displaying the levator
11 Magnetic Resonance and Traditional Radiology in the Diagnosis of... 175
Fig. 4 Sagittal T2-weighted image shows the orientation of (a) oblique axial and (b) oblique coronal planes (white lines), according to, respectively, anal canal short and long axes
plates, which are used as a landmark to separate supra-levator from infra-levator disease. Coronal images allow evaluating the height of the internal opening with the caveat that the anal canal must be imaged along its entire cranio-caudal extent (Halligan 2020).
In our institution the protocol for the evaluation of perianal stulas consists of the following sequences: oblique axial T1-weighted FSE, oblique axial T2-weighted FSE, and oblique axial and oblique coronal fat-suppressed T1-weighted FSE with gadolinium-based contrast material, oriented perpendicular or parallel (in the case of the latter) to the long axis of the anal canal.
T2-weighted sequences are crucial in assessing the perianal disease, due to their exceptional soft tissue contrast, allowing appropriate distinction of the anatomic boundaries between the internal and external sphincters (Figs. 5 and 6). All patho­logical processes (stulas, including every secondary stulous track, and uid collections) can be clearly identied (Baskan et al. 2014). Active stulas have a characteristic aspect, with a central high-signal-intensity tract surrounded by a low­signal-intensity wall (Dwarkasing et al. 2005). The inner high-signal-intensity region of stulas represents the true lumen with granulation tissue, and the external part of stulas with lower signal intensity indicates brotic tissue (Dwarkasing et al.
2005). Therefore, active stulous tracks and extensions have high signal intensity on
T2-weighted images, and they can be easily distinguished from the sphincters and muscles, which have low signal intensity (de Miguel Criado et al. 2012; Balcı et al.
2019). Fat suppression sequences help the differentiation from the surrounding
pelvic fat, which also appears hyperintense (Balcı et al. 2019). Abscesses have also high signal intensity on T2-weighted images due to the presence of purulent
176 L. M. Minordi et al.
Fig. 5 (a) Sagittal T2-weighted image, (b) axial T2-weighted image, (c) axial fat-suppressed T2-weighted image, (d) coronal T2-weighted image, (e) coronal fat-suppressed T2-weighted
11 Magnetic Resonance and Traditional Radiology in the Diagnosis of... 177
Fig. 6 A 53-year-old man. (a) Axial T2-weighted image, (b, c axial contrast-enhanced fat-suppressed T1-weighted images show a trans-sphincteric stula with an internal opening at 11 o’clock position and directed anteriorly towards scrotum (white arrows)
secretions in the central cavity (de Miguel Criado et al. 2012). Having both high signal intensity on T2-weighted image, it may be difcult to assess stulous tracts with a concomitant acute abscess, and some underlying stula tracks may be obscured (Baskan et al. 2014). The low-signal-intensity areas are expected to increase over time as a stula becomes more chronic, indicating the forming of an increasing quantity of brotic tissue (Dwarkasing et al. 2005).
ä
Fig. 5 (continued) image, (f, g) axial and coronal contrast-enhanced fat-suppressed T1-weighted images show a right posterolateral inter-sphincteric stula, conned within external sphincter (white arrows)
178 L. M. Minordi et al.
Unenhanced T1-weighted images allow a detailed anatomic overview of the sphincter complex, levator plate, and ischiorectal fossa. However, both pathological areas (stulous tracks, inammation, and abscesses) and normal structures (such as the sphincters and levator ani muscles) have low-intermediate-signal intensity and may not be differentiated. Unenhanced T1-weighted images can clearly reveal the presence of hemorrhage in the early postoperative phase (de Miguel Criado et al.
2012; Baskan et al. 2014; Balcı et al. 2019); hemorrhage produces high signal
intensity on T1-weighted images and therefore can be distinguished from the lower signal of the residual tracks (de Miguel Criado et al. 2012). Hemorrhagic material can also be differentiated from active granulation tissue having hemorrhage a high signal intensity in T1-weighted images, contrasting the low signal intensity due to the presence of uid or pus in the granulation tissue (de Miguel Criado et al.
2012).
The routine MRI protocol for the anorectal disease usually comprehends a gadolinium contrast-enhanced study (Figs. 5 and 6). This is due to its advantage of rapid dynamic acquisition of data during enhancement of the inammatory tracts and associated abscess (Baskan et al. 2014; Balcı et al. 2019). Normal anorectal struc­tures usually do not enhance signicantly on gadolinium-enhanced fat-suppressed T1-weighted images. Internal anal sphincter and blood vessels (including hemor­rhoidal vessels) are an exception; there fore, they should not be mistaken for stulous tracks or uid collections. At contrast-enhanced fat-suppressed T1-weighted imag­ing, a stula can distinctly be identied as well as its extensions and its relationship to the anal canal, especially to the external sphincter. It is relatively simple to assess the extension of a stula, whether it is contained within the external sphincter or has extended beyond it. The uid inside the track is hypointense, while the stulous tracks and active granulation tissue produce intense enhancement. A plausible reason for high signal intensity within the stulous track on contrast-enhanced fat-suppressed T1-weighted images is the presence of hemorrhagic material from recent surgical intervention; however, this nding is not related to contrast enhance­ment. Abscesses are seen as a central area of low signal intensity due to purulent material that is surrounded by intense ring enhancement. On the other hand, chronic stulas and brotic tissue do not enhance with gadolinium contrast material (de Miguel Criado et al. 2012). T1-weighted contrast-enhanced fat-suppressed MRI sequences are used to differentiate inamed and normal perineal tissues as well as uid and scarring/granulation tissue, which is an important aspect in the imaging characterization of an abscess (Baskan et al. 2014).
Fibrotic stula tracks and scars appear typically as linear structures producing low signal intensity on T1- and T2-weighted images with no signicant enhancement after administration of contrast material (de Miguel Criado et al. 2012).
Diffusion-weighted imaging (DWI) provides functional information regarding the motion of water molecules, tissue cellularity, and the integrity of the cellular membranes. Additionally to its many oncologic applications, DWI is demonstrating promising results in the evaluation of inammation. In fact, DWI was proven to be able to assess the in
ammatory activity in patients with Crohns disease (Oto et al.
2009; Oussalah et al. 2010).