Radiographic Evaluation of Arthritis: Inflammatory Conditions1
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Synovial Joints Permit Movements of the Skeleton
8 Joints Lecture Presentation by Lori Garrett © 2018 Pearson Education, Inc. Section 1: Joint Structure and Movement Learning Outcomes 8.1 Contrast the major categories of joints, and explain the relationship between structure and function for each category. 8.2 Describe the basic structure of a synovial joint, and describe common accessory structures and their functions. 8.3 Describe how the anatomical and functional properties of synovial joints permit movements of the skeleton. © 2018 Pearson Education, Inc. Section 1: Joint Structure and Movement Learning Outcomes (continued) 8.4 Describe flexion/extension, abduction/ adduction, and circumduction movements of the skeleton. 8.5 Describe rotational and special movements of the skeleton. © 2018 Pearson Education, Inc. Module 8.1: Joints are classified according to structure and movement Joints, or articulations . Locations where two or more bones meet . Only points at which movements of bones can occur • Joints allow mobility while preserving bone strength • Amount of movement allowed is determined by anatomical structure . Categorized • Functionally by amount of motion allowed, or range of motion (ROM) • Structurally by anatomical organization © 2018 Pearson Education, Inc. Module 8.1: Joint classification Functional classification of joints . Synarthrosis (syn-, together + arthrosis, joint) • No movement allowed • Extremely strong . Amphiarthrosis (amphi-, on both sides) • Little movement allowed (more than synarthrosis) • Much stronger than diarthrosis • Articulating bones connected by collagen fibers or cartilage . Diarthrosis (dia-, through) • Freely movable © 2018 Pearson Education, Inc. Module 8.1: Joint classification Structural classification of joints . Fibrous • Suture (sutura, a sewing together) – Synarthrotic joint connected by dense fibrous connective tissue – Located between bones of the skull • Gomphosis (gomphos, bolt) – Synarthrotic joint binding teeth to bony sockets in maxillae and mandible © 2018 Pearson Education, Inc. -
Arthritis and Coeliac Disease
Ann Rheum Dis: first published as 10.1136/ard.44.9.592 on 1 September 1985. Downloaded from Annals of the Rheumatic Diseases 1985, 44, 592-598 Arthritis and coeliac disease J T BOURNE,' P KUMAR,2 E C HUSKISSON,' R MAGEED 3 D J UNSWORTH,3 AND J A WOJTULEWSKI4 From the Departments of 'Rheumatology and 2Gastroenterology, St Bartholomew's Hospital, West Smithfield, London ECIA 7BE; the 3Bone and Joint Research Unit, London Hospital Medical College, London El; and 4St Mary's Hospital, Eastbourne SUMMARY We report six patients with coeliac disease in whom arthritis was prominent at diagnosis and who improved with dietary therapy. Joint pain preceded diagnosis by up to three years in five patients and 15 years in one patient. Joints most commonly involved were lumbar spine, hips, and knees (four cases). In three cases there were no bowel symptoms. All were seronegative. X-rays were abnormal in two cases. HLA-type Al, B8, DR3 was present in five and B27 in two patients. Circulating immune complexes showed no consistent pattern before or after treatment. Coeliac disease was diagnosed in all patients by jejunal biopsy, and joint symptoms in all responded to a gluten-free diet. Gluten challenge (for up to three weeks) failed to provoke arthritis in three patients tested. In a separate study of 160 treated coeliac patients attending regular follow up no arthritis attributable to coeliac disease and no ankylosing was in a group spondylitis identified, though control of 100 patients with Crohn's disease thecopyright. expected incidence of seronegative polyarthritis (23%) and ankylosing spondylitis (5%) was found (p<0.01). -
Monitoring Methods of Human Body Joints: State-Of-The-Art and Research Challenges
sensors Review Monitoring Methods of Human Body Joints: State-of-the-Art and Research Challenges Abu Ilius Faisal 1, Sumit Majumder 1 , Tapas Mondal 2, David Cowan 3, Sasan Naseh 1 and M. Jamal Deen 1,* 1 Department of Electrical and Computer Engineering, McMaster University, Hamilton, ON L8S 4L8, Canada; [email protected] (A.I.F.); [email protected] (S.M.); [email protected] (S.N.) 2 Department of Pediatrics, McMaster University, Hamilton, ON L8S 4L8, Canada; [email protected] 3 Department of Medicine, St. Joseph’s Healthcare Hamilton, Hamilton, ON L8N 4A6, Canada; [email protected] * Correspondence: [email protected]; Tel.: +1-905-5259-140 (ext. 27137) Received: 26 April 2019; Accepted: 4 June 2019; Published: 10 June 2019 Abstract: The world’s population is aging: the expansion of the older adult population with multiple physical and health issues is now a huge socio-economic concern worldwide. Among these issues, the loss of mobility among older adults due to musculoskeletal disorders is especially serious as it has severe social, mental and physical consequences. Human body joint monitoring and early diagnosis of these disorders will be a strong and effective solution to this problem. A smart joint monitoring system can identify and record important musculoskeletal-related parameters. Such devices can be utilized for continuous monitoring of joint movements during the normal daily activities of older adults and the healing process of joints (hips, knees or ankles) during the post-surgery period. A viable monitoring system can be developed by combining miniaturized, durable, low-cost and compact sensors with the advanced communication technologies and data processing techniques. -
Conditions Related to Inflammatory Arthritis
Conditions Related to Inflammatory Arthritis There are many conditions related to inflammatory arthritis. Some exhibit symptoms similar to those of inflammatory arthritis, some are autoimmune disorders that result from inflammatory arthritis, and some occur in conjunction with inflammatory arthritis. Related conditions are listed for information purposes only. • Adhesive capsulitis – also known as “frozen shoulder,” the connective tissue surrounding the joint becomes stiff and inflamed causing extreme pain and greatly restricting movement. • Adult onset Still’s disease – a form of arthritis characterized by high spiking fevers and a salmon- colored rash. Still’s disease is more common in children. • Caplan’s syndrome – an inflammation and scarring of the lungs in people with rheumatoid arthritis who have exposure to coal dust, as in a mine. • Celiac disease – an autoimmune disorder of the small intestine that causes malabsorption of nutrients and can eventually cause osteopenia or osteoporosis. • Dermatomyositis – a connective tissue disease characterized by inflammation of the muscles and the skin. The condition is believed to be caused either by viral infection or an autoimmune reaction. • Diabetic finger sclerosis – a complication of diabetes, causing a hardening of the skin and connective tissue in the fingers, thus causing stiffness. • Duchenne muscular dystrophy – one of the most prevalent types of muscular dystrophy, characterized by rapid muscle degeneration. • Dupuytren’s contracture – an abnormal thickening of tissues in the palm and fingers that can cause the fingers to curl. • Eosinophilic fasciitis (Shulman’s syndrome) – a condition in which the muscle tissue underneath the skin becomes swollen and thick. People with eosinophilic fasciitis have a buildup of eosinophils—a type of white blood cell—in the affected tissue. -
Still Disease
University of Massachusetts Medical School eScholarship@UMMS Open Access Articles Open Access Publications by UMMS Authors 2019-02-17 Still Disease Juhi Bhargava Medstar Washington Hospital Center Et al. Let us know how access to this document benefits ou.y Follow this and additional works at: https://escholarship.umassmed.edu/oapubs Part of the Immune System Diseases Commons, Musculoskeletal Diseases Commons, Pathological Conditions, Signs and Symptoms Commons, Skin and Connective Tissue Diseases Commons, and the Viruses Commons Repository Citation Bhargava J, Panginikkod S. (2019). Still Disease. Open Access Articles. Retrieved from https://escholarship.umassmed.edu/oapubs/3764 Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 License. This material is brought to you by eScholarship@UMMS. It has been accepted for inclusion in Open Access Articles by an authorized administrator of eScholarship@UMMS. For more information, please contact [email protected]. Treasure Island (FL): StatPearls Publishing; 2019 Jan-. Still Disease Juhi Bhargava; Sreelakshmi Panginikkod. Author Information Last Update: February 17, 2019. Go to: Introduction Adult Onset Still's Disease (AOSD) is a rare systemic inflammatory disorder characterized by daily fever, inflammatory polyarthritis, and a transient salmon-pink maculopapular rash. AOSD is alternatively known as systemic onset juvenile idiopathic arthritis. Even though there is no specific diagnostic test, a serum ferritin level more than 1000ng/ml is common in AOSD. Go to: Etiology The etiology of AOSD is unknown. The hypothesis remains that AOSD is a reactive syndrome in which various infectious agents may act as triggers in a genetically predisposed host. Both genetic factors and a variety of viruses, bacteria like Yersinia enterocolitica and Mycoplasma pneumonia and other infectious factors have been suggested as important[1][2]. -
Hypersensitivity Reactions (Types I, II, III, IV)
Hypersensitivity Reactions (Types I, II, III, IV) April 15, 2009 Inflammatory response - local, eliminates antigen without extensively damaging the host’s tissue. Hypersensitivity - immune & inflammatory responses that are harmful to the host (von Pirquet, 1906) - Type I Produce effector molecules Capable of ingesting foreign Particles Association with parasite infection Modified from Abbas, Lichtman & Pillai, Table 19-1 Type I hypersensitivity response IgE VH V L Cε1 CL Binds to mast cell Normal serum level = 0.0003 mg/ml Binds Fc region of IgE Link Intracellular signal trans. Initiation of degranulation Larche et al. Nat. Rev. Immunol 6:761-771, 2006 Abbas, Lichtman & Pillai,19-8 Factors in the development of allergic diseases • Geographical distribution • Environmental factors - climate, air pollution, socioeconomic status • Genetic risk factors • “Hygiene hypothesis” – Older siblings, day care – Exposure to certain foods, farm animals – Exposure to antibiotics during infancy • Cytokine milieu Adapted from Bach, JF. N Engl J Med 347:911, 2002. Upham & Holt. Curr Opin Allergy Clin Immunol 5:167, 2005 Also: Papadopoulos and Kalobatsou. Curr Op Allergy Clin Immunol 7:91-95, 2007 IgE-mediated diseases in humans • Systemic (anaphylactic shock) •Asthma – Classification by immunopathological phenotype can be used to determine management strategies • Hay fever (allergic rhinitis) • Allergic conjunctivitis • Skin reactions • Food allergies Diseases in Humans (I) • Systemic anaphylaxis - potentially fatal - due to food ingestion (eggs, shellfish, -
Juvenile Idiopathic Arthritis Associated Uveitis
children Review Juvenile Idiopathic Arthritis Associated Uveitis Emil Carlsson 1,*, Michael W. Beresford 1,2,3, Athimalaipet V. Ramanan 4, Andrew D. Dick 5,6,7 and Christian M. Hedrich 1,2,3,* 1 Department of Women’s and Children’s Health, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool L14 5AB, UK; [email protected] 2 Department of Rheumatology, Alder Hey Children’s NHS Foundation Trust Hospital, Liverpool L14 5AB, UK 3 National Institute for Health Research Alder Hey Clinical Research Facility, Alder Hey Children’s NHS Foundation Trust Hospital, Liverpool L14 5AB, UK 4 Bristol Royal Hospital for Children & Translational Health Sciences, University of Bristol, Bristol BS2 8DZ, UK; [email protected] 5 Translational Health Sciences, University of Bristol, Bristol BS2 8DZ, UK; [email protected] 6 UCL Institute of Ophthalmology, London EC1V 9EL, UK 7 NIHR Biomedical Research Centre, Moorfields Eye Hospital, London EC1V 2PD, UK * Correspondence: [email protected] (E.C.); [email protected] (C.M.H.); Tel.: +44-151-228-4811 (ext. 2690) (E.C.); +44-151-252-5849 (C.M.H.) Abstract: Juvenile idiopathic arthritis (JIA) is the most common childhood rheumatic disease. The development of associated uveitis represents a significant risk for serious complications, including permanent loss of vision. Initiation of early treatment is important for controlling JIA-uveitis, but the disease can appear asymptomatically, making frequent screening procedures necessary for patients at risk. As our understanding of pathogenic drivers is currently incomplete, it is difficult to assess which JIA patients are at risk of developing uveitis. -
Reactive Arthritis Information Booklet
Reactive arthritis Reactive arthritis information booklet Contents What is reactive arthritis? 4 Causes 5 Symptoms 6 Diagnosis 9 Treatment 10 Daily living 16 Diet 18 Complementary treatments 18 How will reactive arthritis affect my future? 19 Research and new developments 20 Glossary 20 We’re the 10 million people living with arthritis. We’re the carers, researchers, health professionals, friends and parents all united in Useful addresses 25 our ambition to ensure that one day, no one will have to live with Where can I find out more? 26 the pain, fatigue and isolation that arthritis causes. Talk to us 27 We understand that every day is different. We know that what works for one person may not help someone else. Our information is a collaboration of experiences, research and facts. We aim to give you everything you need to know about your condition, the treatments available and the many options you can try, so you can make the best and most informed choices for your lifestyle. We’re always happy to hear from you whether it’s with feedback on our information, to share your story, or just to find out more about the work of Versus Arthritis. Contact us at [email protected] Registered office: Versus Arthritis, Copeman House, St Mary’s Gate, Chesterfield S41 7TD Words shown in bold are explained in the glossary on p.20. Registered Charity England and Wales No. 207711, Scotland No. SC041156. Page 2 of 28 Page 3 of 28 Reactive arthritis information booklet What is reactive arthritis? However, some people find it lasts longer and can have random flare-ups years after they first get it. -
Joint Pain and Sjögren’S Syndrome
Joint Pain and Sjögren’s Syndrome Alan N. Baer, MD, FACP Alan N. Baer, MD, FACP Associate Professor of Medicine Division of Rheumatology Johns Hopkins University School of Medicine Director, Jerome Greene Sjogren's Syndrome Clinic 5200 Eastern Avenue Mason F. Lord Bldg. Center Tower Suite 4100, Room 413 Baltimore MD 21224 Phone (410) 550-1887 Fax (410) 550-6255 In 1930, Henrik Sjögren, a Swedish ophthalmologist, examined a woman with rheumatoid arthritis who had extreme dryness of her eyes and mouth and filamentary keratitis, an eye condition related to her lack of tears (1). He became fascinated by this unusual debilitating condition and subsequently evaluated 18 additional women with the same combination of findings. He described this new syndrome as “keratoconjunctivitis sicca” in his postdoctoral thesis. Thirteen of the 19 women had chronic inflammatory arthritis. We would now classify these 13 women as having secondary Sjögren’s syndrome (SS), occurring in the context of rheumatoid arthritis. However, joint pain constitutes one of the most common symptoms of the primary form of SS, defined as SS occurring in the absence of an underlying rheumatic disease. In a recent survey of SS patients belonging to the French Sjögren’s Syndrome Society (Association Française du Gougerot-Sjögren et des Syndromes Secs), 81% reported significant joint and muscle pain (2). In this article, the joint manifestations of primary SS will be reviewed. A few definitions are needed for the reader. Although the term “arthritis” was originally applied to conditions causing joint inflammation, it now includes disorders in which the joint has become damaged by degenerative, metabolic, or traumatic processes. -
Adult-Onset Still's Disease
Journal of Clinical Medicine Review Adult-Onset Still’s Disease: Clinical Aspects and Therapeutic Approach Stylianos Tomaras 1,* , Carl Christoph Goetzke 2,3,4 , Tilmann Kallinich 2,3,4 and Eugen Feist 1 1 Department of Rheumatology, Helios Clinic Vogelsang-Gommern, 39245 Gommern, Germany; [email protected] 2 Department of Pediatrics, Division of Pulmonology, Immunology and Critical Care Medicine, Charité–Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), 10117 Berlin, Germany; [email protected] (C.C.G.); [email protected] (T.K.) 3 German Rheumatism Research Center (DRFZ), Leibniz Association, 10117 Berlin, Germany 4 Berlin Institute of Health, 10178 Berlin, Germany * Correspondence: [email protected] Abstract: Adult-onset Still’s disease (AoSD) is a rare systemic autoinflammatory disease charac- terized by arthritis, spiking fever, skin rash and elevated ferritin levels. The reason behind the nomenclature of this condition is that AoSD shares certain symptoms with Still’s disease in children, currently named systemic-onset juvenile idiopathic arthritis. Immune dysregulation plays a central role in AoSD and is characterized by pathogenic involvement of both arms of the immune system. Furthermore, the past two decades have seen a large body of immunological research on cytokines, which has attributed to both a better understanding of AoSD and revolutionary advances in treatment. Additionally, recent studies have introduced a new approach by grouping patients with AoSD into only two phenotypes: one with predominantly systemic features and one with a chronic articular Citation: Tomaras, S.; Goetzke, C.C.; disease course. -
A Dash of Dermatology and a Pinch of Rheumatology
A dash of dermatology and a pinch of rheumatology Sarita Nori, MD, FAAD Dermatology Atrius Health I have no conflicts of interest to disclose. 2 . Points in white = fun factoids . Points in blue = important for clinical practice; practice gaps. (Basically what you want to remember from this talk.) OUTLINE . Some clinical pearls . Treatment . Diagnosis . Update in Dermatology: . Biologics for Psoriasis - because many of your patients are on these meds now. Biologic for Atopic dermatitis – finally something new! Treatment pearls . For all itch/dermatitis: maximize anti histamines. - Zyrtec/Claritin/Allegra bid, - plus Benadryl or Hydroxyzine qhs, with intent of sedation Poison ivy - Can avoid oral steroids. Use higher topical steroids TID, + maximal anti histamines. - Poison ivy adjunct care: important to dissolve the oil from all objects that may have been exposed. Eg pets, pet collars & leashes, gardening gloves, hats, socks, shoes, watch straps, earrings etc. This is often why the rash seems to get worse despite treatment, or spreads a lot, or recurs even though it was getting better Treatment pearls . Tinea versicolor: > treat with Diflucan 400mg po x 2 doses, 1 week apart. Pityriasis Rosea: > Acyclovir 800mg 5 times /day x 1 week => 79% pts cleared by day 14. Das et al. Indian Dermatol Online J. 2015 May-Jun; 6(3): 181–184. • Seb derm on scalp/psoriasis on scalp/dandruff/itchy scalp: Ketoconazole shampoo daily, clobetasol solution qd for 2-4 weeks • Testing in allergy dept is not = skin allergy testing (patch testing). Skin contact allergies develop after multiple exposures, so not usually a new exposure. 6 MORE TREATMENT PEARLS . -
Guideline on Clinical Investigation of Medicinal Products for the Treatment of Rheumatoid Arthritis
14 December 2017 CPMP/EWP/556/95 Rev. 2 Committee for Medicinal Products for Human Use (CHMP) Guideline on clinical investigation of medicinal products for the treatment of rheumatoid arthritis Draft Agreed by Rheumatology-Immunology Working Party (RIWP) December 2011 Adoption by CHMP for release for consultation 5 December 2011 End of consultation (deadline for comments) 05 June 2012 Agreed by Rheumatology-Immunology Working Party (RIWP) March 2015 Adoption by CHMP 20 March 2015 Start of public consultation 4 June 2015 End of consultation (deadline for comments) 29 November 2015 Agreed by Rheumatology-Immunology Working Party (RIWP) 24 November 2017 Adoption by CHMP 14 December 2017 Date of coming into effect 01 July 2018 This guideline replaces the “Points to consider on the clinical investigation of medicinal products other than NSAIDS in rheumatoid arthritis (CPMP/EWP/556/95 REV. 1)” Keywords Rheumatoid arthritis, Disease Modifying Anti-Rheumatic Drugs, clinical development, CHMP, EMA, guideline 30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact An agency of the European Union © European Medicines Agency, 2018. Reproduction is authorised provided the source is acknowledged. Guideline on clinical investigation of medicinal products for the treatment of rheumatoid arthritis Table of contents List of abbreviations .................................................................................... 3 Executive