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Relevant bibliographies by topics / Sacroiliite

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Academic literature on the topic 'Sacroiliite'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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Journal articles on the topic "Sacroiliite"

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Bart, G., M. Plat, N. Derouet, and E. Dernis. "Sacroiliite infectieuse du post-partum." Médecine et Maladies Infectieuses 43, no. 10 (October 2013): 431–33. http://dx.doi.org/10.1016/j.medmal.2013.07.011.

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Fagart, A. "La sacroiliite inflammatoire en TEMP/TDM osseuse." Médecine Nucléaire 42, no. 4 (July 2018): 224–36. http://dx.doi.org/10.1016/j.mednuc.2018.05.002.

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Pratte, Laurence, and Pierre-Louis Docquier. "Sacroiliite infectieuse chez l’enfant : un diagnostic difficile. Quatre cas." Revue du Rhumatisme 76, no. 5 (May 2009): 482–84. http://dx.doi.org/10.1016/j.rhum.2008.09.022.

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Amor, Bernard. "La sacroiliite est-elle indispensable au diagnostic de Spondylarthrite ?" Revue du Rhumatisme 76, no. 8 (September 2009): 813–17. http://dx.doi.org/10.1016/j.rhum.2009.03.014.

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Bou Antoun, Myriame, Catherine Adamsbaum, Luca Semerano, Isabelle Koné-Paut, and Linda Rossi-Semerano. "Prédicteurs cliniques de sacroiliite détectée par IRM chez les enfants atteints d’enthésite avec arthrite." Revue du Rhumatisme 85, no. 6 (December 2018): 574–78. http://dx.doi.org/10.1016/j.rhum.2018.02.001.

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Ait Sahel, O., A. Biyi, Y. Benameur, H. Bouyaallaoui, and A. Doudouh. "Valeur ajoutée d’une acquisition TEMP/TDM centrée sur le bassin complétant une scintigraphie osseuse dans un cas de sacroiliite à pyogène." Médecine Nucléaire 41, no. 2 (March 2017): 126–30. http://dx.doi.org/10.1016/j.mednuc.2017.01.004.

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Fain, O., C. Taleb, N. Feton, M. Sibony, F. Lejeune, and M. Thomas. "Syndrome de Sweet à localisation digestive, vascularite, abcès du psoas et sacroiliite: manifestations révélatrices d'une anémie réfractaire avec excès de blastes évoluant rapidement vers une leucémie aiguë." La Revue de Médecine Interne 13, no. 7 (December 1992): S460. http://dx.doi.org/10.1016/s0248-8663(05)81039-2.

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Tornero, C., M. D. C. Castro Villegas, X. Juanola-Roura, M. L. García-Vivar, C. Fernández-Carballido, J. F. Garcia Llorente, B. Joven-Ibáñez, E. Galindez, C. Urrego-Laurín, and E. De Miguel. "FRI0324 NO RADIOGRAPHIC SACROILIITIS PROGRESSION OVER 6 YEARS IN PATIENTS WITH EARLY SPONDYLOARTHRITIS FROM THE ESPERANZA COHORT." Annals of the Rheumatic Diseases 79, Suppl 1 (June 2020): 754.2–754. http://dx.doi.org/10.1136/annrheumdis-2020-eular.5450.

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Background:Longitudinal studies about the change from non-radiographic axial Spondyloarthritis (nr-axSpA) to r-axSpA (radiographic axial Spondyloarthritis) are scarce but show a 9-10% progression rate over 2 years (1-2) and a 24% progression rate over 10 years in another study (3). However, in early cohorts such as DESIR, this only represents a 5% over 5 years (4).Objectives:The aim of this study was to know the rate of progression from nr-axSpA to r-axSpA over 6 years in the early Esperanza cohort.Methods:This study included 94 patients of the Spanish early spondyloarthritis (SpA) Esperanza cohort, 60 fulfilled the ASAS classification criteria for SpA. Every patient had a baseline and a six years sacroiliac X-ray. Nine readers, blinded for the diagnosis, participated in the reliability exercise, all of them experienced rheumatologists and members of the Spanish spondyloarthritis working group (GRESSER). Patients with SpA were classified as having r-axSpA, at baseline or after 6 years of follow-up, if they fulfilled the radiographic item of the modified New York criteria (mNY) (presence of radiographic changes in the sacroiliac joints -SIJ- of at least grade II bilaterally or grade III or IV unilaterally). The gold standard of SIJ X-Ray was the categorical opinion of at least five of the expert readers. For the statistical analysis, the Chi-square and Kappa tests were performed.Results:Demographic data of the SpA patients were: mean age 33.4±7.5 years; 37 (61.7%) male; mean CRP 6.4±6.5 mg/dl and ESR 10.3±10.6. Present smokers 30.6%; and past smokers 16.3%. HLA-B27 (+) 56.7%. Regarding the presence of X-Ray sacroilitis: 20 patients had baseline sacroilitis and 18 at the final visit; 11 had sacroiliitis at both baseline and final visits; 9 patients changed from baseline sacroiliitis to no-sacroiliitis and 7 changed from baseline no-sacroiliitis to sacroiliitis at the 6 year visit. The reliability of the readers was fair with a mean inter-reader kappa test of 0.375 (range 0.146 - 0.652) and a mean agreement of 73.7% (range 58.7% - 90%).Conclusion:In this group of patients with early SpA no progression from nr-axSpA to r-axSpA over 6 years was observed. It appears that early diagnosis and standard treatment seem to reduce SIJ radiographic progression.References:[1]Poddubnyy D, Rudwaleit M, Haibel H, et al. Rates and predictors of radiographic sacroiliitis progression over 2 years in patients with axial spondyloarthritis. Ann Rheum Dis 2011;70:1369–74.[2]Sampaio-Barros PD, Conde RA, Donadi EA, et al. Undifferentiated spondyloarthropathies in Brazilians: importance of HLA-B27 and the B7-CREG alleles in characterization and disease progression. J Rheumatol 2003;30:2632–7.[3]Sampaio-Barros PD, Bortoluzzo AB, Conde RA, et al. Undifferentiated spondyloarthritis: a longterm followup. J Rheumatol 2010;37:1195–9.[4]Dougados M, et al. Ann Rheum Dis 2017;76:1823–1828.Disclosure of Interests:Carolina Tornero: None declared, María del Carmen Castro Villegas: None declared, Xavier Juanola-Roura: None declared, Maria Luz García-Vivar: None declared, Cristina Fernández-Carballido Consultant of: Yes, I have received fees for scientific advice (Abbvie, Celgene, Janssen, Lilly and Novartis), Speakers bureau: Yes, I have received fees as a speaker (Abbvie, Celgene, Janssen, Lilly, MSD, Novartis), Jose Francisco Garcia LLorente: None declared, Beatriz Joven-Ibáñez Speakers bureau: Abbvie, Celgene, Janssen, Merck Sharp & Dohme, Novartis, Pfizer, E. Galindez: None declared, Claudia Urrego-Laurín: None declared, Eugenio de Miguel Grant/research support from: Yes (Abbvie, Novartis, Pfizer), Consultant of: Yes (Abbvie, Novartis, Pfizer), Paid instructor for: yes (AbbVie, Novartis, Pfizer, MSD, BMS, UCB, Roche, Grunental, Janssen, Sanofi), Speakers bureau: yes (AbbVie, Novartis, Pfizer, MSD, BMS, UCB, Roche, Grunental, Janssen, Sanofi)

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Luxembourger, C., Y. Degboé, A. Cantagrel, D. Nigon, P. Claudepierre, A. Constantin, and A. Ruyssen-Witrand. "Association entre les polymorphismes des gènes ERAP1, IL23R et TRAILR1 et la présence d’une sacroiliite magnétique chez les patients atteints de spondyloarthrite axiale récente : données issues de la cohorte française DESIR." Revue du Rhumatisme 83 (November 2016): A117—A118. http://dx.doi.org/10.1016/s1169-8330(16)30387-8.

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Geijer, M., G. Gadeholt Göthlin, and J. H. Göthlin. "Observer variation in computed tomography of the sacroiliac joints: a retrospective analysis of 1383 cases." Acta Radiologica 48, no. 6 (July 2007): 665–71. http://dx.doi.org/10.1080/02841850701342146.

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Background: Computed tomography (CT) for evaluation of sacroiliitis has a higher diagnostic accuracy than radiography. There is a high degree of interobserver variation in evaluating sacroiliitis on radiographs. Purpose: To evaluate interobserver variation in CT of the sacroiliac joints for evaluation of sacroiliitis in a large number of patients. Material and Methods: 1383 CT examinations of the sacroiliac joints were reviewed by two observers. The outcomes as originally reported and the findings from the reviews were classified as no sacroiliitis, equivocal, unilateral sacroiliitis, or bilateral sacroiliitis. The unweighted kappa statistic was used for assessment of observer agreement. Results: The interobserver agreement between the two reviewers was good (κ = 0.6724), with excellent agreement on cases of bilateral sacroiliitis and moderate agreement on cases of unilateral sacroiliitis. Excellent agreement was also reached in normal cases. Compared to the original reports, there were moderate interobserver agreements between both reviewers' findings and the original reports (κ = 0.4651 and κ = 0.4481, respectively). Conclusion: The interobserver variation for the diagnosis of sacroiliitis on CT between two reviewers in a study setting showed good agreement, with moderate agreement between each of the observers and the original clinical reports. CT is a reliable method for evaluating the sacroiliac joints for changes of sacroiliitis.

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Dissertations / Theses on the topic "Sacroiliite"

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BUISSET, HERVE. "Sacro-iliite ou spondylodiscite au cours d'une endocardite : a propos de deux observations, revue de la litterature." Lille 2, 1988. http://www.theses.fr/1988LIL2M083.

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Echinard, Marie-Thérèse. "Sacro iliite à eikenella corrodens : (à propos d'une observation)." Bordeaux 2, 1989. http://www.theses.fr/1989BOR25150.

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Books on the topic "Sacroiliite"

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van Gaalen, Floris, Désirée van der Heijde, and Maxime Dougados. Diagnosis and classification of axial spondyloarthritis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198734444.003.0003.

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Axial spondyloarthritis (axSpA) is a potentially disabling chronic inflammatory disease affecting the spine and sacroiliac (SI) joints. Lead symptoms are chronic back pain and stiffness. The disease is called radiographic axSpA or ankylosing spondylitis (AS) when, on plain radiographs, bone changes consistent with sacroiliitis are present. When no evidence of sacroiliitis is seen on radiographs, it is called non-radiographic axSpA. In such cases, diagnosis is made based on evidence of active inflammation of SI joints on magnetic resonance imaging (MRI) and clinical and laboratory features, or a combination of clinical and laboratory features only. Apart from affecting the spine and SI joints, axSpA may involve peripheral joints (e.g. knee, ankle) and manifest in extra-articular manifestations, for example uveitis, psoriasis, and inflammatory bowel disease. In this chapter, diagnosis and classification of axSpA is discussed, including use of MRI in detecting sacroiliitis and the difference between clinical diagnosis and disease classification.

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Bawa, Sandeep, Paul Wordsworth, and Inoshi Atukorala. Spondyloarthropathies. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.010004.

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♦ Spondyloarthropathies are related conditions typically associated with axial skeletal involvement, absence of rheumatoid factor, familial clustering, and a variable positive association with HLA-B27♦ Ankylosing spondylitis is the prototype with sacroiliac joint involvement being a prerequisite for diagnosis♦ Diagnosis is frequently delayed for several years but the use of magnetic resonance imaging to detect sacroiliitis greatly facilitates the establishment of an early diagnosis♦ Psoriatic arthritis, reactive arthritis, and enteropathic arthritis have prominent peripheral joint involvement with variable degrees of spinal involvement♦ Non-steroidal anti-inflammatory drugs and physical therapy are the cornerstones of management but slow-acting disease-modifying antirheumatic drugs only have a role in peripheral arthritis♦ Anti-tumour necrosis factor biologic agents have revolutionized the treatment of the spondyloarthropathies.

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Maksymowych, Walter P., and Robert G. W. Lambert. Imaging: sacroiliac joints. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198734444.003.0013.

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Radiography of the sacroiliac (SI) joints still forms the cornerstone of diagnosis of axial spondyloarthritis (axSpA), although its limitations in early disease preclude early diagnosis. Equivocal radiographic findings of sacroiliitis should be followed by MRI evaluation of the SI joints, especially if clinical suspicion of SpA is high. Routine diagnostic evaluation for SpA by MRI of the SI joints should include simultaneous evaluation of T1-weighted (T1W) and short tau inversion recovery (STIR) or T2 fat-suppressed scans. Bone marrow oedema (BME) in subchondral bone is the primary MRI feature that points to the diagnosis of SpA, although structural lesions such as erosion and fat metaplasia may also be evident in early disease and enhance confidence in the diagnosis. Both inflammatory and structural lesions in the SI joints on MRI can now be quantified in a reliable manner to facilitate therapeutic evaluation in clinical trials and for basic and clinical research.

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Rudwaleit, Martin. Enthesitis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0054.

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Enthesitis is one of the key manifestations of spondyloarthritides (SpA) including ankylosing spondylitis (AS) and psoriatic arthritis. Enthesitis can occur alone or in combination with peripheral arthritis, sacroiliitis, or spondylitis. The inflammatory process is typically located at the insertion of the enthesis or ligament to bone, often resulting in osteitis as well. Because of its anatomical and functional complexity the term 'enthesis organ' has been coined. Biomechanical stress applied to the enthesis seems to play an important role for the occurrence of enthesitis in genetically predisposed individuals. Ultrasound imaging of peripheral entheses reveals enthesis abnormalities including entheseal calcification, bony erosion, or bony proliferation. Power Doppler signals demonstrating increased vascularization of inflamed entheses at the insertional site appear to be the most characteristic finding for enthesitis, yet study results are conflicting. Enthesitis-related osteitis and enthesitis at the spine is best visualized by MRI. Enthesitis may resolve spontaneously or may run a chronic course. Standard treatment includes local steroid injections, non-steroidal anti-inflammatory drugs (NSAIDs), and physical therapy. There is little evidence for the efficacy of disease-modifying anti-rheumatic drugs (DMARDs) in enthesitis. In contrast, anti-TNF agents have proven efficacy, and their use in treatment-resistant enthesitis is recommended in the Assessment of SpondyloArthritis international Society (ASAS)/European League Against Rheumatism (EULAR) recommendations for the management of AS and axial SpA and in the EULAR recommendations for psoriatic arthritis.

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Rudwaleit, Martin. Enthesitis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0054_update_002.

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Enthesitis is one of the key manifestations of spondyloarthritis (SpA) including ankylosing spondylitis (AS) and psoriatic arthritis. Enthesitis can occur alone or in combination with peripheral arthritis, sacroiliitis, or spondylitis. The inflammatory process is typically located at the insertion of the enthesis or ligament to bone, often resulting in osteitis as well. Because of its anatomical and functional complexity the term ’enthesis organ’ has been coined. Biomechanical stress applied to the enthesis seems to play an important role for the occurrence of enthesitis in genetically predisposed individuals. Ultrasound imaging of peripheral entheses reveals enthesis abnormalities including entheseal calcification, bony erosion, or bony proliferation. Power Doppler signals demonstrating increased vascularization of inflamed entheses at the insertional site appear to be the most characteristic finding for enthesitis, yet study results are conflicting. Enthesitis-related osteitis and enthesitis at the spine is best visualized by MRI. Enthesitis may resolve spontaneously or may run a chronic course. Standard treatment includes local steroid injections, non-steroidal anti-inflammatory drugs (NSAIDs), and physical therapy. There is little evidence for the efficacy of disease-modifying antirheumatic drugs (DMARDs) in enthesitis. In contrast, anti-TNF agents have proven efficacy, and their use in treatment-resistant enthesitis is recommended in the Assessment of SpondyloArthritis international Society (ASAS)/European League Against Rheumatism (EULAR) recommendations for the management of AS and axial SpA and in the EULAR recommendations for psoriatic arthritis.

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Tillett, William, and Neil McHugh. Plain radiography. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198737582.003.0016.

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Psoriatic arthritis is a destructive inflammatory arthritis that can affect the peripheral and axial skeleton of patients with psoriasis. Plain radiography has formed an important part in defining psoriatic arthritis as a distinct clinical entity, from early work reporting on distinguishing features to more recent inclusion of osteoproliferation in the CASPAR classification criteria. Plain radiography is accessible, inexpensive and remains the standard measure of assessing damage in inflammatory arthritis. Originally considered a benign disease psoriatic arthritis is now recognised to be destructive and progressive, though not as aggressive as rheumatoid arthritis. Peripheral joint damage is characterised by erosions, joint space narrowing, osteoproliferation, osteolysis and ankylosis. Approximately twenty percent of patients have erosive disease at diagnosis progressing to approximately half of all patients by three years disease duration. In its most severe form, psoriatic arthritis mutilans, digits become shortened from gross bone resorption (osteolyisis) leading to severe functional impairment and disability. Spondyloarthritis may affect between 25-70% of patients with PsA. The radiographic features of Psoriatic Spondyloarthritis differ from Ankylosing Spondylitis, in that sacroiliitis is often asymmetrical and less severe, the cervical spine is frequently involved and syndesmophytes are asymmetrical and para-marginal. Overall radiographic features are less severe than ankylosing spondylitis. The natural history of both peripheral and axial radiographic damage in psoriatic arthritis in the modern era of early diagnosis, tight disease control and biologic drugs has yet to be established.

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Sieper, Joachim. Ankylosing spondylitis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0113.

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Ankylosing spondylitis (AS) is a chronic inflammatory disease predominantly of the sacroiliac joint (SIJ) and the spine. It starts normally in the second decade of life and has a slight male predominance. The prevalence is between 0.2 and 0.8% and is strongly dependent on the prevalence of HLA B27 in a given population. For the diagnosis of AS, the presence of radiographic sacroiliitis is mandatory. However, radiographs do not detect active inflammation but only structural bony damage. Most recently new classification criteria for axial spondyloarthritis (SpA) have been developed by the Assessement of Spondylo-Arthritis international Society (ASAS) which cover AS but also the earlier form of non-radiographic axial SpA. MRI has become an important new tool for the detection of subchondral bone marrow inflammation in SIJ and spine and has become increasingly important for an early diagnosis. HLA B27 plays a central role in the pathogenesis but its exact interaction with the immune system has not yet been clarified. Besides pain and stiffness in the axial skeleton patients suffer also from periods of peripheral arthritis, enthesitis, and uveitis. New bone formation as a reaction to inflammation and subsequent ankylosis of the spine determine long-term outcome in a subgroup of patients. Currently only non-steroidal anti-inflammatory drugs (NSAIDs) and tumour necrosis factor (TNF) blockers have been proven to be effective in the medical treatment of axial SpA, and international ASAS recommendations for the structured management of axial SpA have been published based on these two types of drugs. Conventional disease-modifying anti-rheumatic drugs (DMARDs) such as methotrexate are not effective.

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Sieper, Joachim. Axial spondyloarthropathies. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0113_update_003.

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Axial spondyloarthritis (axSpA) is a chronic inflammatory disease predominantly of the sacroiliac joint (SIJ) and the spine. It starts normally in the second decade of life and has a slight male predominance. The prevalence is between 0.2% and 0.8% and is strongly dependent on the prevalence of HLA-B27 in a given population. AxSpA can be split in patients with radiographic axSpA (also termed ankylosing spondylitis (AS)) and in patients with non-radiographic axSpA (nr-axSpA). For the diagnosis of AS, the presence of radiographic sacroiliitis is mandatory. However, radiographs do not detect active inflammation but only structural bony damage. Most recently new classification criteria for axSpA have been developed by the Assessment of Spondylo-Arthritis International Society (ASAS) which cover AS but also the earlier form of nr-axSpA. MRI has become an important new tool for the detection of subchondral bone marrow inflammation in SIJ and spine and has become increasingly important for an early diagnosis. HLA-B27 plays a central role in the pathogenesis but its exact interaction with the immune system has not yet been clarified. Besides pain and stiffness in the axial skeleton patients suffer also from periods of peripheral arthritis, enthesitis, and uveitis. New bone formation as a reaction to inflammation and subsequent ankylosis of the spine determine long-term outcome in a subgroup of patients. Currently only non-steroidal anti-inflammatory drugs (NSAIDs) and tumour necrosis factor (TNF) blockers have been proven to be effective in the medical treatment of axial SpA, and international ASAS recommendations for the structured management of axial SpA have been published based on these two types of drugs. Conventional disease-modifying anti-rheumatic drugs (DMARDs) such as methotrexate are not effective.

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Book chapters on the topic "Sacroiliite"

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Chien, George C. Chang, Radhika P. Grandhe, and Joseph D. Fortin. "Sacroiliitis and Sacroiliac Joint Dysfunction." In Treatment of Chronic Pain Conditions, 265–68. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6976-0_77.

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Faleiros, Matheus Calil, José Raniery Ferreira Junior, Eddy Zavala Jens, Vitor Faeda Dalto, Marcello Henrique Nogueira-Barbosa, and Paulo Mazzoncini de Azevedo-Marques. "Pattern Recognition of Inflammatory Sacroiliitis in Magnetic Resonance Imaging." In VipIMAGE 2017, 639–44. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-68195-5_69.

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Fenton, Douglas S. "Sacroiliitis." In Imaging Painful Spine Disorders - Expert Consult, 476–81. Elsevier, 2011. http://dx.doi.org/10.1016/b978-1-4160-2904-5.00063-x.

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Vilensky, Joel A., Edward C. Weber, Thomas E. Sarosi, and Stephen W. Carmichael. "Sacroiliitis." In Medical Imaging of Normal and Pathologic Anatomy, 117. Elsevier, 2010. http://dx.doi.org/10.1016/b978-1-4377-0634-5.00117-6.

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"Sacroiliitis." In Encyclopedia of Pain, 3435. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-28753-4_102046.

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"Sacroiliitis, Unilateral." In Expertddx: Musculoskeletal, 360–61. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-52483-4.50099-5.

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"Infectious Sacroiliitis." In MRI of the Musculoskeletal System, edited by Martin Vahlensieck, Harry K. Genant, Maximilian Reiser, James O. Johnston, and Steinborn. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0034-51213.

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"Sacroiliitis, Bilateral Symmetric." In Expertddx: Musculoskeletal, 354–57. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-52483-4.50097-1.

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"Sacroiliitis, Bilateral Asymmetric." In Expertddx: Musculoskeletal, 358–59. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-52483-4.50098-3.

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"Computerized tomography of sacroiliitis." In Classic Papers in Rheumatology, 34–35. CRC Press, 2001. http://dx.doi.org/10.3109/9780203214237-17.

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Conference papers on the topic "Sacroiliite"

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CAVALCANTE, ANAUÁ FERNANDA DOS SANTOS, JHÉSYCA CASTAMAN STÉDILE, THIAGO ALBERTO G. SANTOS, THELMA LAROKE SKARE, DEBORAH CRISTYNE COLOMBO ITO, and JULIANA DELFINO. "SACROILITIS IN A PATIENT WITH SARCOIDOSIS: CASE REPORT." In 36º Congresso Brasileiro de Reumatologia. São Paulo: Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-234.

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Ben Abla, H., S. rekik, S. boussaid, H. ajlani, H. sahli, I. cheour, and M. elleuch. "AB1048 Evolution of infectious sacroiliitis according to the germ." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.7557.

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Faleiros, Matheus Calil, José Raniery Ferreira Junior, Eddy Javala Jens, Vitor Faeda Dalto, Marcello Henrique Nogueira-Barbosa, and Paulo Mazzoncini De Azevedo-Marques. "Reconhecimento Computadorizado de Padrões Inflamatórios de Sacroiliíte em Imagens de Ressonância Magnética." In XVII Simpósio Brasileiro de Computação Aplicada à Saúde. Sociedade Brasileira de Computação - SBC, 2017. http://dx.doi.org/10.5753/sbcas.2017.3731.

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O método referência para avaliar a inflamação nas articulações sacroilíacas (AS) em espondiloartrites é a ressonância magnética (RM). Porém, ele pode apresentar desafios para especialistas devido a sua variabilidade clínica. Neste contexto, este trabalho visa reconhecer padrões inflamatórios de AS em imagens de RM utilizando atributos de níveis de cinza, textura e espectrais. Os atributos foram extraídos de 51 pacientes e selecionados pelo método ReliefF. A classificação foi realizada por métodos de aprendizado de máquina e avaliados pelaárea sob a curva ROC utilizando validação cruzada 10-fold. Resultados mostraram que o método de cinco vizinhos próximos apresentou maior precisão do que os outros classificadores.

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Forbes, J. N., S. W. Frederick, M. Y. Savage, and A. R. Cross. "Infectious Sacroiliitis in Conjunction with Brucella canis in a Dog." In Abstracts of the 46th Annual Conference of the Veterinary Orthopedic Society. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1692283.

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Ghozlan, R., M. Dupuis, J. Mani, and S. Marciano. "AB0128 Usefulness of mri for the diagnosis of inflammatory sacroiliitis." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.337.

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PINHEIRO, AYSA, PAULA TOCHE, CLAUDIA MARQUES, NARA CAVALCANTI, JONAS BRAYNER, GEORGIA PEREIRA, JOSE OTAMIR ANDRADE JR, and ANGELA DUARTE. "SJOGREN SYNDROME WITH SACROILIITIS OR SPONDYLOARTHRITIS WITH SIALADENITIS? A CASE SERIES." In 36º Congresso Brasileiro de Reumatologia. São Paulo: Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-254.

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LAVOR, DANIELE, and KELLE CAMBOIM. "TUBERCULOUS SACROILIITIS SECONDARY TO HEMATOGENOUS DISSEMINATION OF PULMONARY TUBERCULOSIS: CASE REPORT." In 36º Congresso Brasileiro de Reumatologia. São Paulo: Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-300.

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OLIVEIRA, SAMILY CORDEIRO DE, ANTONIO HELDER COSTA VASCONCELOS, MARCIO VALE BRAGA, CARLOS LEITE DE MACEDO FILHO, JAILSON RODRIGUES LOPES, and CARLOS EWERTON MAIA RODRIGUES. "EVALUATION OF SACROILIITIS BY MAGNETIC RESONANCE IMAGING IN PATIENTS WITH PSORIASIC ARTHRITIS." In 36º Congresso Brasileiro de Reumatologia. São Paulo: Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-439.

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Stefanović, L., D. Veljković, E. Mahmutović, and V. Skakić. "AB0774 Prevalence, clinical and radiographic characteristics of sacroilitis in patients with psoriasis." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.6737.

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Bubová, Kristýna, Monika Gregová, Kateřina Zegzulková, Karel Pavelka, Jarmila Heissigerová, and Ladislav Šenolt. "THU0373 ACTIVE SACROILIITIS ON MAGNETIC RESONANCE IMAGING IN PATIENTS WITH ANTERIOR UVEITIS." In Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.7439.

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Reports on the topic "Sacroiliite"

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Zvonorencko, M. S., E. V. Kalinina, and A. R. Babaeva. SACROILITIS IN METABOLIC DISEASES: CLINICAL OBSERVATION. Планета, 2018. http://dx.doi.org/10.18411/978-5-907109-24-7-2018-xxxv-180-183.

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