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Advanced cervical DOM with extension beyond the discovertebral complex. Sagittal T2 (A), sagittal (B), and axial (C) T1 post contrast MR images coned in to the mid cervical spine show characteristic MR features of C5-C6 DOM with advanced disc and endplate destruction. In addition, there is prominent ventral epidural extension of phlegmonous infection (arrow in A-C) contributing to spinal canal stenosis and spinal cord compression. C) Axial T1-post contrast image best demonstrates the right more than left ventral and lateral paraspinous extension of infection without drainable fluid collection.

Advanced cervical DOM with extension beyond the discovertebral complex. Sagittal T2 (A), sagittal (B), and axial (C) T1 post contrast MR images coned in to the mid cervical spine show characteristic MR features of C5-C6 DOM with advanced disc and endplate destruction. In addition, there is prominent ventral epidural extension of phlegmonous infection (arrow in A-C) contributing to spinal canal stenosis and spinal cord compression. C) Axial T1-post contrast image best demonstrates the right more than left ventral and lateral paraspinous extension of infection without drainable fluid collection.

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... There is moderate T2 hyperintensity, but the hallmark is extensive diffuse contrast enhancement secondary to enhancing fibroconnective granulation tissue changes and phlegmonous changes. This type of enhancement is seen in approximately 70% of cases with SEA [17]. The phlegmonous accumulation within the SES can result in a significant mass effect on the dural sac and can completely encase the dural sac. ...
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Purpose of Review The goal of this review is to summarize the importance of identifying and treating a spinal epidural abscess. This review also delves into the intricacies of imaging modalities and the controversies regarding management options. Recent Findings Although magnetic resonance imaging (MRI) is a valuable diagnostic tool for evaluating SEA, focused attention to T2 imaging to the exclusion of other sequences can result in diagnostic errors and overlooking critical epidural abscesses. Summary Spinal epidural abscess is a rare disease; however, it has high morbidity and mortality if left untreated. Although rare, there is a slow progressive increase in the incidence of SEA. Imaging should be considered for any patient with red flags in their history or physical examination. MRI is the imaging test of choice to assure early diagnosis and treatment. Reliance on T2 imaging can result in an underappreciation of SEA. The characteristic space-occupying process, the essential comparison of T1 and T2 imaging, and the use of contrast characteristics are key ingredients for an accurate diagnosis.
... Computed tomography (CT) scan may be performed in addition to MRI. CT scans can provide superior evaluation of bony abnormalities such as end plate and vertebral body erosion, as well as assessment of overall bone quality [27] . Additionally, when a causative organism cannot be obtained from blood cultures, CT-guided biopsy may be necessary to guide antimicrobial treatment. ...
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... Spinal infections, discitis-osteomyelitis (DOM) and septic facet joints may affect the paraspinal region in many ways: reactive inflammation, pyomyositis and abscesses can occur in the epaxial muscles around the affected joint (Fig. 11) [111]. DOM is often associated with paraspinal soft tissue abnormalities, especially in hypaxial muscles, Muscle contusion of the right erector spinae muscle in a 27-year-old male after bicycle accident (c). ...
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... Associated medical co-morbidities and risk factors found in patients with spondylodiscitis were concurrent infection in 35% of cases, cardiovascular disease in 24% of cases, diabetes in 20% of cases, intravenous drug use in 15% of cases, and immunosuppression in 11% of cases [4]. Alcohol abuse was a contributing comorbidity in 19.2% of cases [1] as well as concurrent malignancy as a common medical comorbidity in 11% of cases [2]. The average age of presentation was found to be 63.3 and 66.6 in two population studies, while it was 58.3 in a meta-analysis [1,2,4]. ...
... Magnetic resonance imaging (MRI) has a specificity of 94%, sensitivity of 96%, and accuracy of 92% and is thought to be the imaging modality of choice for diagnosing infections of the spine [14,16,17]. Expected imaging changes are decreased T1 intensity from involved areas, increased T2-weighted intensity, and gadolinium enhancement of the infected disc, vertebrae, and surrounding soft tissues [13,14,16,17] Although MRI is the choice of imaging for diagnosis of spinal infections, computed tomography (CT) can be performed to better elucidate bone anatomy; which can assist in determining if surgical intervention is indicated [14,18,19]. CT scans are also often used for guidance for needle biopsies, if indicated [14]. ...
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... MRI contrast study is the gold standard for spinal infections.MR imaging is very much useful in early stages of infection when other modalities are either normal or nonspecific [5] . MRI contrast study is especially helpful for anatomical localization and early diagnosis of spinal infections [18] . ...
... 1,2,3,5 The challenge of detecting this uncommon signal from a great deal of background noise can result in diagnostic delay, which can lead to the progression of unrecognized sepsis, permanent neurologic deficit for the patient, and increasing medicolegal risk for the physician. [5][6][7][8][9][10] Although magnetic resonance imaging (MRI) with gadolinium contrast is 96% sensitive and 93% specific for PSI, it is not an easily administered test. It requires 4-8 hours for test results, 11 is uncomfortable in some patients, contributes to ED crowding, and is not available at all facilities where back pain is evaluated. ...
... It requires 4-8 hours for test results, 11 is uncomfortable in some patients, contributes to ED crowding, and is not available at all facilities where back pain is evaluated. 6,10,12,13 Currently there are no clinical prediction tools to estimate PSI risk, [14][15][16][17] no agreement on C-reactive protein (CRP) cut-off levels to indicate imaging, 18 and no uniform recommendations regarding MRI use. 13,19 Recent publications recommend imaging spine pain patients who have any of the following PSI risk features: historical risk factors; fever; history of fever or progressive neurological deficit, 2,6,7,17,20,21 and to consider an alternate diagnosis if none of these are present. ...
... Eighty-three percent (25/30) of PSI patients with neurological deficits had no fever to prompt consideration of infection among the 89 spinal infections, highlighting a key circumstance where infection could be overlooked. The algorithm in Figure 3 considers this by using current published recommendations of contrast-enhanced MRI in patients suspected of infection, 3,9,10,12,13,21 as indicated by SIRCH score ≥3. For those with a neurological deficit, who are at low risk for infection (SIRCH score of <3), current recommendations indicate that MRI (without contrast) is the appropriate imaging modality. ...
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... Its sensitivity is 96%, and specificity is 93% for an accuracy of 94%. An infection will show as a region of low T1 and high T2 signal intensity, with post-contrast enhancement on fat-suppressed T1-weighted images ( Figure 2) [20,21]. There is increased FDG uptake in the bone and soft tissues immediately adjacent to the hardware from T12 to L4 (arrows). ...
... 4. CT-guided biopsy: Spinal biopsy for cultures is not routinely done, and therapy is usually guided by clinical and radiological findings, but in chronic cases, atypical cases, and cases not clinically responding to IV antibiotic, a CT-guided biopsy can yield an organism if blood cultures were negative, which can determine the activity of the disease and guide treatment [18]. The success rate of CT-guided biopsy in finding an organism is between 36% and 91% [1], compared to a yield of 76% for open surgical biopsy [21]. ...
... On MRI, the presence of multiple vertebral levels involvement with intervening normal levels (skip lesions) is suggestive of tuberculosis over pyogenic spondylodiscitis ( Figure 5) [21]. ...
... Its sensitivity is 96%, and specificity is 93% for an accuracy of 94%. An infection will show as a region of low T1 and high T2 signal intensity, with post-contrast enhancement on fat-suppressed T1-weighted images ( Figure 2) [20,21]. There is increased FDG uptake in the bone and soft tissues immediately adjacent to the hardware from T12 to L4 (arrows). ...
... 4. CT-guided biopsy: Spinal biopsy for cultures is not routinely done, and therapy is usually guided by clinical and radiological findings, but in chronic cases, atypical cases, and cases not clinically responding to IV antibiotic, a CT-guided biopsy can yield an organism if blood cultures were negative, which can determine the activity of the disease and guide treatment [18]. The success rate of CT-guided biopsy in finding an organism is between 36% and 91% [1], compared to a yield of 76% for open surgical biopsy [21]. ...
... On MRI, the presence of multiple vertebral levels involvement with intervening normal levels (skip lesions) is suggestive of tuberculosis over pyogenic spondylodiscitis ( Figure 5) [21]. ...
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... The challenge of detecting this uncommon signal from a great deal of background noise can 42 result in diagnostic delay, which can lead to the progression of unrecognized sepsis, permanent 43 neurologic deficit for patients, and increasing medical-legal risk for physicians. [5][6][7][8][9][10] Although 44 magnetic resonance imaging (MRI) with gadolinium contrast is 96% sensitive and 93% specific progressive neurological deficit, 2,6,7,17,20,21 and to consider an alternate diagnosis if none of these 53 are present. 2,6,20,21 54 55 Goals of this Investigation 56 We aimed to develop an intuitive risk prediction score using history, physical examination, 57 and CRP measurement that provides a sensitive assessment of the risk of PSI and appropriately 58 recommends MRI. ...
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The paper describes a derived prediction model that estimates the probability of pyogenic spinal infection in ED patients with back or neck pain.
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