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Juvenile Spondyloarthropathies: Inflammation in Disguise
PP.qxd:06/15-2 Ped Perspectives 7/25/08 10:49 AM Page 2 APEDIATRIC Volume 17, Number 2 2008 Juvenile Spondyloarthropathieserspective Inflammation in DisguiseP by Evren Akin, M.D. The spondyloarthropathies are a group of inflammatory conditions that involve the spine (sacroiliitis and spondylitis), joints (asymmetric peripheral Case Study arthropathy) and tendons (enthesopathy). The clinical subsets of spondyloarthropathies constitute a wide spectrum, including: • Ankylosing spondylitis What does spondyloarthropathy • Psoriatic arthritis look like in a child? • Reactive arthritis • Inflammatory bowel disease associated with arthritis A 12-year-old boy is actively involved in sports. • Undifferentiated sacroiliitis When his right toe starts to hurt, overuse injury is Depending on the subtype, extra-articular manifestations might involve the eyes, thought to be the cause. The right toe eventually skin, lungs, gastrointestinal tract and heart. The most commonly accepted swells up, and he is referred to a rheumatologist to classification criteria for spondyloarthropathies are from the European evaluate for possible gout. Over the next few Spondyloarthropathy Study Group (ESSG). See Table 1. weeks, his right knee begins hurting as well. At the rheumatologist’s office, arthritis of the right second The juvenile spondyloarthropathies — which are the focus of this article — toe and the right knee is noted. Family history is might be defined as any spondyloarthropathy subtype that is diagnosed before remarkable for back stiffness in the father, which is age 17. It should be noted, however, that adult and juvenile spondyloar- reported as “due to sports participation.” thropathies exist on a continuum. In other words, many children diagnosed with a type of juvenile spondyloarthropathy will eventually fulfill criteria for Antinuclear antibody (ANA) and rheumatoid factor adult spondyloarthropathy. -
Atraumatic Bilateral Achilles Tendon Rupture: an Association of Systemic
378 Kotnis, Halstead, Hormbrey Acute compartment syndrome may be a of the body of gastrocnemius has been result of any trauma to the limb. The trauma is reported in athletes.7 8 This, however, is the J Accid Emerg Med: first published as 10.1136/emj.16.5.378 on 1 September 1999. Downloaded from usually a result of an open or closed fracture of first reported case of acute compartment the bones, or a crush injury to the limb. Other syndrome caused by a gastrocnemius muscle causes include haematoma, gun shot or stab rupture in a non-athlete. wounds, animal or insect bites, post-ischaemic swelling, vascular damage, electrical injuries, burns, prolonged tourniquet times, etc. Other Conclusion causes of compartment syndrome are genetic, Soft tissue injuries and muscle tears occur fre- iatrogenic, or acquired coagulopathies, infec- quently in athletes. Most injuries result from tion, nephrotic syndrome or any cause of direct trauma. Indirect trauma resulting in decreased tissue osmolarity and capillary per- muscle tears and ruptures can cause acute meability. compartment syndrome in athletes. It is also Chronic compartment syndrome is most important to keep in mind the possibility of typically an exercise induced condition charac- similar injuries in a non-athlete as well. More terised by a relative inadequacy of musculofas- research is needed to define optimal manage- cial compartment size producing chronic or ment patterns and potential strategies for recurring pain and/or disability. It is seen in injury prevention. athletes, who often have recurring leg pain that Conflict of interest: none. starts after they have been exercising for some Funding: none. -
Modic Type 1 Changes: Detection Performance of Fat-Suppressed
Musculoskeletal System Modic Type 1 Changes: Detection Performance of Fat-Suppressed Fluid-Sensitive MRI Sequences Modic-Typ-1-Endplattenveränderungen: Detektionsrate mittels fettgesättigten, flüssigkeitssensitiven MRT- Sequenzen Authors Tim Finkenstaedt1,FilippoDelGrande2, Nicolae Bolog3, Nils Ulrich4,SinaTok4,OrpheusKolokythas5, Johann Steurer6, Gustav Andreisek1, Sebastian Winklhofer1, 7, on behalf of the LSOS Study Group Affiliations keitssensitiven MRT-Sequenzen gegenüber Standard T1- und 1 Institute of Diagnostic and Interventional Radiology, T2-gewichteten Sequenzen an der Lendenwirbelsäule zu ver- University Hospital Zurich, University of Zurich, Zurich, gleichen. Switzerland Material und Methoden Sagittale T1, T2 und fettgesät- 2 Institute of Diagnostic and Interventional Radiology, tigte, flüssigkeitssensitive MRT-Sequenzen von 100 Patienten Ospedale Regionale di Lugano, Lugano, Switzerland (gesamt 500 Wirbelsegmente; 52 weiblich, Durchschnitts- 3 Phoenix Diagnostic Clinic, Bucharest, Romania alter 74 ± 7,4 Jahre; 48 männlich, Durchschnittsalter 71 ± 6,3 4 Department of Neurosurgery, Spine Center, Schulthess Jahre) wurden retrospektiv untersucht. Das Vorhandensein Clinic, Zurich, Switzerland (ja/nein) und die Ausdehnung (Likert-skalierte Höhen-, Volu- 5 Institute for Radiology and Nuclear Medicine, men- und anteroposteriore Endplattenausdehnung) von Kantonsspital Winterthur, Winterthur, Switzerland Modic-1-Veränderungen auf T1/T2 gegenüber fettgesättig- 6 Horten Center for patient oriented research and ten, flüssigkeitssensitiven -
The Endplate and Trabecular Bone in Lumbar Degenerative Disc Disease: a Narrative Review
SN Comprehensive Clinical Medicine (2020) 2:332–337 https://doi.org/10.1007/s42399-020-00234-y SURGERY The Endplate and Trabecular Bone in Lumbar Degenerative Disc Disease: A Narrative Review Tom Marjoram1 Accepted: 29 January 2020 /Published online: 6 February 2020 # The Author(s) 2020 Abstract To review the current knowledge surrounding degenerative disc disease focusing on the changes taking place in the end plate and trabecular bone. A narrative review of the current literature. An age-related reduction in blood supply to the disc contributes to tissue degradation. Degeneration, separate from this process, represents a disruption of the normal homeostasis. A process of vascular and sensory nerve in-growth in the annulus and localised areas of the end plate is associated with markers of inflam- mation and may represent a pain source. Treatment with local anti-inflammatories has, at best, mixed results. Bone mechanical indentation testing has been used to classify changes in ageing and degeneration demonstrating a location-dependant reduction in strength specific to each process. Modic changes include a process of inflammation, alteration of the mechanical and chemical environment and changes in bone turnover. The underlying cause for their development has multiple explanations including mechanical overload and microfracture, infection and inflammation in response to herniation of disc material through the end plate. We do know, however, that they seem to be at least partially reversible and not all are symptomatic. This reversibility potentially indicates an avenue of exploration for therapy. Restoring the complex balance of disc homeostasis may hold some promise and will rely on greater understanding of the pathological and material changes occurring at the disc-bone interface and their correlation with clinical imaging. -
Juvenile Spondyloarthritis / Enthesitis Related Arthritis (Spa-ERA) Version of 2016
https://www.printo.it/pediatric-rheumatology/GB/intro Juvenile Spondyloarthritis / Enthesitis Related Arthritis (SpA-ERA) Version of 2016 1. WHAT IS JUVENILE SPONDYLOARTHRITIS/ENTHESITIS- RELATED ARTHRITIS (SpA-ERA) 1.1 What is it? Juvenile SpA-ERA constitutes a group of chronic inflammatory diseases of the joints (arthritis), as well as tendon and ligament attachments to certain bones (enthesitis) and affects predominantly the lower limbs and in some cases the pelvic and spinal joints (sacroiliitis - buttock pain and spondylitis - back pain). Juvenile SpA-ERA is significantly more common in people that have a positive blood test for the genetic factor HLA-B27. HLA-B27 is a protein located on the surface of immune cells. Remarkably, only a fraction of people with HLA-B27 ever develops arthritis. Thus, the presence of HLA-B27 is not enough to explain the development of the disease. To date, the exact role of HLA-B27 in the origin of the disease remains unknown. However, it is known that in very few cases the onset of arthritis is preceded by gastrointestinal or urogenital infection (known as reactive arthritis). Juvenile SpA-ERA is closely related to the spondyloarthritis with onset in adulthood and most researchers believe these diseases share the same origin and characteristics. Most children and adolescents with juvenile spondyloarthritis would be diagnosed as affected by ERA and even psoriatic arthritis. It is important that the names "juvenile spondyloarthritis", "enthesitis-related arthritis" and in some cases "psoriatic arthritis" may be the same from a clinical and therapeutic point of view. 1 / 12 1.2 What diseases are called juvenile SpA-ERA? As mentioned above, juvenile spondyloarthritis is the name for a group of diseases; the clinical features may overlap with each other, including axial and peripheral spondyloarthritis, ankylosing spondylitis, undifferentiated spondyloarthritis, psoriatic arthritis, reactive arthritis and arthritis associated with Crohn’s disease and ulcerative colitis. -
Abstract Book 2021
MAY 31 – JUNE 1: COMMITTEE MEETINGS JUNE 2‐4: SCIENTIFIC PROGRAM ABSTRACT BOOK Oral presentations at the ISSLS Virtual Annual Meeting, May 31‐June 4, 2021 O01 Human Lumbar Discs are not sterile! - Defining the Normal Intervertebral Disc Microbiome Shanmuganathan Rajasekaran1, Soundararajan Dilip Chand Raja1, Tangavel Chitraa2, Nayagam Sharon Miracle2, Muthurajan Raveendran3, Matchado Monica Steffi2, K S Vijayanand1 1. Ganga hospital, Coimbatore, TAMIL NADU, India 2. Department of Proteomics, Ganga Research Centre, Coimbatore, Tamil Nadu, India 3. Department of Plant Biology , Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu, India Introduction: Traditionally, Central Nervous System, spinal cord, eye, fetus and Intervertebral Disc were considered to be to be sterile and immune privileged. With the advent of 16SrRNA sequencing, it has been proved that each of the above have a microbiome which plays an essential role in maintaining homeostasis. With increasing reports of sub-clinical infection as an etiology of disc degeneration and Modic changes, it remains unknown, whether lumbar discs are truly sterile. The primary aim of the study was to investigate the presence of Disc microbiome and its microbial composition. Materials and Methods: In order to obtain true normal controls, intervertebral discs were collected from MRI normal brain-dead voluntary organ donors with no history of back pain. The study was performed after the approval of IRB. The discs were dissected in surgical sterile conditions and were snap frozen immediately to -160⁰C and the processed samples were subjected to total DNA extraction using QIAamp® DNA Mini Kit and enrichment using NEBNext® Microbiome DNA Enrichment Kit (Cat # E612S/L; New England BioLabs, Ipswich, MA). -
The Correlations Between Dimensions of the Normal Tendon And
www.nature.com/scientificreports OPEN The correlations between dimensions of the normal tendon and tendinopathy changed Achilles tendon in routine magnetic resonance imaging Pawel Szaro 1,2,3* & Khaldun Ghali Gataa2 This comparative study aimed to investigate how tendinopathy-related lesions change correlations in the dimensions of the Achilles tendon. Our experimental group included 74 patients. The mean age was 52.9 ± 10.4 years. The control group included 81 patients with a mean age was 35.2 ± 13.6 years, p < .001. The most signifcant diference in correlation was the thickness of the tendon and the midportion’s width, which was more signifcant in the tendinopathy (r = .49 vs. r = .01, p < .001). The correlation was positive between width and length of the insertion but negative in normal tendons (r = .21 vs. r = − .23, p < .001). The correlation was between the midportions width in tendinopathy and the tendon’s length but negative in the normal tendon (r = .16 vs. r = − .23, p < .001). The average thickness of the midportion in tendinopathy was 11.2 ± 3.3 mm, and 4.9 ± 0.5 mm in the control group, p < .001. The average width of the midportion and insertion was more extensive in the experimental group, 17.2 ± 3.1 mm vs. 14.7 ± 1.8 mm for the midportion and 31.0 ± 3.9 mm vs. 25.7 ± 3.0 mm for insertion, respectively, p < .001. The tendon’s average length was longer in tendinopathy (83.5 ± 19.3 mm vs. 61.5 ± 14.4 mm, p < .001). The dimensions correlations in normal Achilles tendon and tendinopathic tendon difer signifcantly. -
Type II Modic Changes May Not Always Represent Fat Degeneration a Study Using MR Fat Suppression Sequence
SPINE Volume 41, Number 16, pp E987–E994 ß 2016 Wolters Kluwer Health, Inc. All rights reserved DIAGNOSTICS Type II Modic Changes May not Always Represent Fat Degeneration A Study Using MR Fat Suppression Sequence Zhiyun Feng, MD,Ã Yuanhao Liu, MD,Ã Wei Wei,y Shengping Hu, MD,y and Yue Wang, PhDÃ (24.7%) type II MCs was suppressed on FS images, that of 113 Study Design. A radiological study of type II Modic changes (75.3%) was not suppressed. The discs adjacent to type II MCs (MCs). had lower signal intensity (0.13 Æ 0.003 vs.0.14Æ 0.004, Objectives. The aim of this study was to determine the P < 0.001), lesser disc height (9.73 Æ 1.97 vs.11.07Æ 1.99, characteristics of type II MCs on fat suppression (FS) magnetic P < 0.001) and greater bulging area (80.0 Æ 31.4 vs. 61.3 Æ 27.5 resonance (MR) images and its association with radiological disc for anterior bulging, 33.72 Æ 21.24 vs. 27.93 Æ 12.79 for degeneration. Summary of Background Data. Type II MCs are common posterior bulging, and 113.7 Æ 39.9 vs. 89.2 Æ 35.2 for total < endplate signal changes on MR images. On the basis of limited bulging, P 0.05) than normal controls. Type II MCs that were histological samples, type II MCs are thought to be stable fat not suppressed on FS image were associated with greater age < degeneration. FS technique on MR, which can quantify fat [odds ratio (OR) ¼ 1.11, P 0.001], lower height (OR ¼ 0.94, < < content, may be an alternative to explore the pathology of MCs. -
Heel Enthesopathy of Diffuse Idiopathic Skeletal Hyperostosis
Images in Rheumatology Heel Enthesopathy of Diffuse Idiopathic Skeletal Hyperostosis Resembling Enthesitis of Spondyloarthritis IGNAZIO OLIVIERI, MD, SALVATORE D’ANGELO, MD, Rheumatology Department of Lucania, San Carlo Hospital, Contrada Macchia Romana, 85100 Potenza, Italy; and Madonna delle Grazie Hospital; FRANCESCO BORRACCIA, Researcher, Radiology Department, San Carlo Hospital; ANGELA PADULA, MD, Senior Researcher, Rheumatology Department of Lucania, San Carlo Hospital, and Madonna delle Grazie Hospital, Matera, Italy. Address correspondence to Dr. Olivieri; E-mail: [email protected]. J Rheumatol 2010;37:192–3; doi.10.3899/jrheum.090514 Diffuse idiopathic skeletal hyperostosis (DISH) and anky- tendons, resembling the typical fusiform soft tissue swelling losing spondylitis (AS) are 2 clearly different disease enti- of Achilles enthesitis of spondyloarthritis5 (Figure 1). ties having in common the involvement of the axial skeleton However, palpation of the region did not reveal any inflam- and the peripheral entheses1,2. Both diseases produce bone matory findings of enthesitis but did reveal bone prolifera- proliferation in the spine and at the extraspinal entheseal tion due to large spurs, a condition confirmed by radio- sites in the later phases of their course. Although the aspects graphs (Figure 2). A sacroiliac joint computed tomography of the bone proliferations of the 2 diseases are dissimilar, (CT) scan showed the normal aspect of joint space and bony confusion of radiographic differential diagnosis between the margins together with the presence of capsular ossifications 2 diseases exists, partly as a consequence of a lack of aware- (Figure 3). ness of their respective characteristic features2,3. It has been pointed out that the differential diagnosis between DISH and REFERENCES longstanding advanced AS is not limited to the radiologic 1. -
Clinical and Imaging Assessment of Peripheral Enthesitis in Ankylosing Spondylitis
Special RepoRt Clinical and imaging assessment of peripheral enthesitis in ankylosing spondylitis Enthesitis, defined as inflammation of the origin and insertion of ligaments, tendons, aponeuroses, annulus fibrosis and joint capsules, is a hallmark of ankylosing spondylitis. The concept of entheseal organ prone to pathological changes in ankylosing spondylitis and other spondyloarthritis is well recognized. The relevant role of peripheral enthesitis is supported by the evidence that this feature, on clinical examination, has been included in the classification criteria of Amor (heel pain or other well-defined enthesopathic pain), European Spondiloarthropathy Study Group and Assessment in SpondyloArthritis International Society for axial and peripheral spondyloarthritis. Nevertheless, the assessment of enthesitis has been improved by imaging techniques to carefully detect morphological abnormalities and to monitor disease activity. 1 Keywords: ankylosing spondylitis n clinical assessment n enthesitis n MrI Antonio Spadaro* , n spondyloarthritis n ultrasound Fabio Massimo Perrotta1, In primary ankylosing spondylitis (AS) the fre- has proven to be a highly sensitive and nonin- Alessia Carboni1 quency of peripheral enthesitis has been found vasive tool to assess the presence of enthesitis, & Antongiulio Scarno1 to be between 25 and 58% [1], however, the real characterized by hypoechogenicity with loss 1Dipartimento di Medicina Interna e prevalence of this feature depends on the type of tendon fibrillar pattern, tendon thickening, Specialità -
Foot Pain & Psoriatic Arthritis
WHEATON • ROCKVILLE • CHEVY CHASE • WASHINGTON, DC Foot Pain & Psoriatic Arthritis Daniel El-Bogdadi, MD, FACR Arthritis and Rheumatism Associates, P.C. Do you feel heel pain in the Plantar fasciitis ARTHRITIS morning or after a period of can be caused by inactivity? This might be an a number AND indication of plantar fasciitis that of factors, RHEUMATISM could be part of an underlying including aerobic ASSOCIATES, P.C. psoriatic arthritis condition. dance exercise, running, and Board Certified Rheumatologists Psoriatic arthritis is an inflammatory ballet. arthritis that typically causes pain, Herbert S.B. Baraf MD FACP MACR swelling and stiffness in the Robert L. Rosenberg peripheral joints or spine. However, MD FACR CCD if you have psoriatic arthritis, you Evan L. Siegel may notice that not only are the MD FACR joints and spine involved, but Emma DiIorio symptoms may also occur in the soft MD FACR tissue such as tendons or ligaments. David G. Borenstein MD MACP MACR This usually happens in a place Alan K. Matsumoto where tendons and ligaments attach There are several treatment options MD FACP FACR to bone, known as the enthesis. for plantar fasciitis: David P. Wolfe When this attachment gets inflamed MD FACR it is called enthesitis. • The first immediate intervention is Paul J. DeMarco MD FACP FACR to decrease or stop any Shari B. Diamond One of the more common areas to repetitive activities, such as MD FACP FACR get enthesitis is in the Achilles running or dancing, which may Ashley D. Beall tendon. Another common area for aggravate the condition. MD FACR inflammation is in thick band of (over) Angus B. -
NIH HEAL Initiative Workshop on Myofascial Pain
Initiative NIH HEAL Workshop on MYOFASCIAL PAIN Quantitative Evaluation of Myofascial Tissues: Potential Impact for Musculoskeletal Pain Research September 16-17, 2020 Co-organizers NIH Partners NCCIH NIAMS NIBIB NICHD/NCMRR NIDCR NINDS Workshop Summary #nihHEALinitiative NIH HEAL Initiative Workshop on Myofascial Pain Quantitative Evaluation of Myofascial Tissues: Potential Impact for Musculoskeletal Pain Research September 16-17, 2020 Welcome Remarks: NIH HEAL Initiative Rebecca Baker, NIH HEAL Director The National Institutes of Health (NIH) Helping to End Addiction Long-termSM (HEAL) Initiative is working to address two related crises affecting the United States: addiction/overdose and chronic pain. In 2018, more than 67,300 Americans died from drug-related overdose, including many affected by opioid addiction. The COVID-19 pandemic appears to be reversing the progress made in this area. Among American adults, 50 million are affected by chronic pain, 25 million report daily severe pain, and 20 million experience high-impact pain that interferes with work and daily life. HEAL receives $500 million/year in sustained research investment. To date, more than 25 HEAL research programs have been funded. HEAL has a trans-NIH governance structure, and research is collaboratively supported by 20 NIH institutes/centers. The two overarching goals of HEAL are to enhance pain management and improve treatment for opioid misuse and addiction. Research is being done in the following areas to meet these goals: preclinical/translational research in pain management, clinical research in pain management, novel medication options, enhanced outcomes for affected newborns, new prevention and treatment strategies, and translation of research into practice. Information on ongoing HEAL projects, workshops, and funding opportunities can be found on the HEAL website.