Medical Pathology: Arthropathies PDF
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Chris Borgman, Wil McGriff
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This document is a lecture on medical pathology, focusing on arthropathies. It covers the pathophysiology and clinical findings of different types of arthropathies. The lecture also touches on lab tests and diagnosis, and mentions some risk factors, signs, symptoms and treatment.
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Medical Pathology: Arthropathies CHRIS BORGMAN, OD ASSOCIATE PROFESSOR [email protected] WIL MCGRIFF, OD, MPH ASSOCIATE PROFESSOR [email protected] Lecture Objectives Understand pathophysiology and clinical findings of non-inflammatory arthropathies. ¡ Osteoarthritis Understand pathophysiolo...
Medical Pathology: Arthropathies CHRIS BORGMAN, OD ASSOCIATE PROFESSOR [email protected] WIL MCGRIFF, OD, MPH ASSOCIATE PROFESSOR [email protected] Lecture Objectives Understand pathophysiology and clinical findings of non-inflammatory arthropathies. ¡ Osteoarthritis Understand pathophysiology and clinical findings of inflammatory arthropathies. ¡ Rheumatoid arthritis, JIA, Gout, Spondylarthropathies Know principles of discussed lab tests and how to use them clinically to diagnose arthropathic conditions. NBEO Outline Musculoskeletal System ¡ 1. Epidemiology ¡ 2. Symptoms and signs of the various arthritic syndromes (e.g., JRA, RA, ankylosing spondylitis) ¡ 3. Diagnostic testing and imaging ¡ 4. Pathophysiology and diagnosis Arthropathies Defn: Diseases of the joints ¡ Non-inflammatory arthropathies (arthrosis) ÷ Osteoarthritis ¡ Inflammatory arthropathies (arthritis) ÷ Rheumatoid arthritis ÷ Juvenile idiopathic arthritis ÷ Gout ÷ Spondyloarthropathies Review: Anatomy/Physiology of Joints 3 main types: ¡ ¡ ¡ Fixed/Fibrous: skull Cartilaginous: intervertebral discs Synovial*: knee, elbow Articular cartilage ¡ Avascular connective tissue surrounding the ends of bones Joint capsule ¡ Membranous sac that encloses the joint Synovium ¡ ¡ Thin membrane inside the joint capsule Secretes synovial fluid Synovial fluid ¡ ¡ Lubricates the joint Nourishes the cartilage Ligaments ¡ ¡ Bone to bone Stabilize the joint Tendons ¡ ¡ Muscles to bones Transmit force from muscles Muscles ¡ Move the joint Arthritis *Inflammation of one or more joints ¡ ¡ >50 million diagnoses in the US Very common disability ÷ >21 million adults (9% US population) Common symptoms: ¡ ¡ ¡ ¡ ¡ Pain Stiffness Decreased range of motion Swelling Redness Systemic associations possible: ¡ ¡ ¡ ¡ Autoimmune (ie. SLE) Infectious (ie. gonorrhea, chlamydia, shigella) Biochemical (ie. gout) Others possible… Osteoarthritis Osteoarthritis Defn: *Mechanical breakdown of articular cartilage ¡ *Most common arthropathy ÷ 10-13% US population (~30 million) Risk Factors: ¡ *Obesity (36.5% USA is obese) ÷ 69% knee replacements in USA 2’ obesity Autoimmune diseases ¡ Increased age; F>M ¡ Previous joint injury ¡ Repetitive motion Signs and Symptoms: ¡ Stiffness after a period of immobility ¡ Joint swelling and/or joint pain ¡ Crunching feeling or the sound of bone rubbing on bone ¡ Osteoarthritis Joints typically affected: ¡ ¡ ¡ ¡ Lifetime Risk of OA ¡ Knee = 46%; Hip = 25% Diagnosis ¡ **Knees (37% >60 yo) *Hips *Hands Spine X-ray/CT/MRI Treatment ¡ ¡ ¡ ¡ ¡ ¡ Exercise (low impact) Weight loss Analgesics Anti-inflammatories Joint Replacement Surgery Physical therapy (PT) Rheumatoid Arthritis Rheumatoid Arthritis *Autoimmune destruction of the joints ¡ Trigger à idiopathic ÷ Genetics? Infection? 1-2% of adult population ¡ F>M (3X) ¡ Average onset = 20-30 yo ¡ Peaks between 30-55 yo ¡ Sn/Sx: mild to severe possible ¡ Periods of remission and exacerbation ¡ Symptoms lessen during pregnancy (70% cases improve) Rheumatoid Arthritis Complications: ¡ Destroys and distorts joints over time ¡ Reduces mobility and QOL ¡ Reduces life expectancy Ulnar deviation Severe Rheumatoid Factor (RF) RF = an IgM Anti-IgG autoantibody ¡ Forms immune complexes à deposit in joints ¡ Inflammatory cells accumulate at sites of deposition ¡ Chronic inflammation à angiogenesis ¡ “Pannus” covers the articular cartilage ¡ Causes bone destruction and joint deformity Labwork: Rheumatoid Arthritis Diagnosis *Rheumatoid factor (RF) ¡ IgM àNonspecific marker for RA; also (+) in SLE, Sjogrens, TB, etc. ¡ 75% of RA patients ¡ High titers = more severe disease *Anti-cyclic citrullinated peptide (CCP) antibody ¡ IgG à Positive in 64-89% of RA patients ¡ More sensitive and specific than RF ¡ Progression/prognosis worse if (+)CCP Antinuclear antibody (ANA) ¡ IgG à 20% of RA patients ¡ Titer is lower than in SLE HLA-DR1 and HLA-DR4 ¡ 60-70% in RA patients Rheumatoid Arthritis Treatment Medication ¡ Disease modifying anti-rheumatic drugs (DMARDs) Methotrexate ÷ Hydroxychloroquine ÷ Gold salts ÷ ¡ Biologics ÷ ¡ Rituximab, Infliximab Anti-inflammatories ÷ Steroids, NSAIDs Physical therapy Exercise Surgery *Ocular Manifestations: ¡ Episcleritis, Scleritis, Iritis, PUK Ocular chrysiasis Juvenile Idiopathic Arthritis Juvenile Idiopathic Arthritis Formerly known as “juvenile rheumatoid arthritis” (JRA) ¡ JRA ≠ Adult RA *Most common childhood arthritis Autoimmune disorder targeting synovium ¡ Chronic inflammation leads to joint damage ¡ Affects ~1 in 1000 children ¡ F>M ¡ *Onset before 16 yo Signs and symptoms: ¡ Joint stiffness/pain ¡ Limited range of motion ¡ Warm, swollen, or red joints ¡ Child may stop using limb or may limp Juvenile Idiopathic Arthritis Systemic symptoms ¡ Fever, usually high fevers every day ¡ Rash that comes and goes with the fever ¡ Pale skin ¡ Malaise ¡ Lymphadenopathy Ocular manifestations ¡ **Anterior uveitis** (~12% of all JIA cases) It is recommended that all children with JIA be screened for iritis ÷ **Most common cause of uveitis in pediatric age group ÷ ¡ SE: Cataracts from steroids Juvenile Idiopathic Arthritis Diagnosis ¡ History & examination ¡ Labwork: Same as adult RA ¡ HLA-B27 à predicts more severe disease if positive too Treatment ¡ Same as adult RA Prognosis is good with early Dx and Tx Gout Gout Acute episodes of painful joint inflammation ¡ *Cause: Uric acid buildup in any joint; (deposits à tophi) ¡ Reduced kidney clearance > increased production ÷ 90% vs. 10% 3 million cases in US ¡ M>F ¡ AA>Caucasian (2X) ¡ Onset 40-50 yo Signs and symptoms ¡ Sudden onset of pain Usually the proximal joint of the great toe in 50% of cases ÷ Initial pain lasts 12-48 hours ÷ ¡ Edema and erythema Gout Excess uric acid Supersaturation Crystal formation Joint degradation Dietary sources of purines ¡ Organ meats ¡ Shellfish/Seafood ¡ Alcohol ¡ Soda drinks Gout Risk factors ¡ Age ¡ Sex ¡ Genetics ¡ Renal disease ¡ Diet ¡ Obesity ¡ Systemic disease ÷ HTN/DM/Hyperlipidemia Diagnosis ¡ Serology (>7 mg/dL) ¡ Urinalysis ¡ Synovial fluid aspiration Treatment (Goal: <6 mg/dL) ¡ Acute Anti-inflammatories ÷ Colchicine ÷ ¡ Prophylactic Allopurinol ÷ Probenecid ÷ ¡ Lifestyle modifications Proper hydration ÷ Decrease alcohol intake ÷ Weight loss ÷ Dietary changes ÷ Spondylarthropathies Spondylarthropathies Types: 1. 2. 3. 4. 5. ¡ Ulcerative Colitis Crohn’s/Inflammatory Bowel Disease-associated SpA Reactive Arthritis Ankylosing Spondylitis Psoriatic Arthritis Acronym: “UCRAP” Spondylarthropathies Defn: Diverse group of chronic inflammatory conditions ¡ *Affect axial and peripheral joints mainly ¡ “Seronegative” for RF and ANA Common features: ¡ Inflammatory back pain ¡ Enthesitis ÷ ¡ Inflammation at sites where tendons, ligaments, and joint capsule fibers attach to bone Extra-articular manifestations Psoriasis ÷ Anterior uveitis/iritis ÷ Inflammatory bowel disease ÷ HLA-B27 Testing Class I major histocompatibility complex molecule Present in only 1.4-8.0% of the general population ¡ Whites>non-whites **Strongly associated with all SpA*** ¡ ~70% of all individuals w/ SpA carry the HLA-B27 gene ¡ Inflammatory bowel disease ÷ ¡ ¡ ¡ (Ulcerative Colitis & Crohn’s) Reactive Arthritis Ankylosing spondylitis Psoriatic arthritis } “UCRAP” 1. Inflammatory Bowel Disease • See GI Tract 2 Lecture Arthritis occurs in 25% of patients 50–60% of patients with IBD and spondylitis will be HLA-B27 positive *Acute anterior uveitis/iritis occurs: ¡ ¡ 5-10% of patients with Ulcerative Colitis 2.5% of patients with Crohn’s Disease Other rare ocular findings seen with IBD include: ¡ Episcleritis ¡ Scleritis ¡ Optic neuritis ¡ Retinal vasculitis 2. Reactive Arthritis (Reiter’s Syndrome) Inflammatory arthritis that is post genitourinary or gastrointestinal infection ¡ ¡ ¡ ¡ Annual prevalence of 1-7% Whites>non-whites Onset 20-50 yo Men>Women ÷ ÷ Equal for enteric 9X greater in men for STD Causative agents ¡ ¡ ¡ ¡ ¡ *Chlamydia (36-61%) Salmonella (6-30%) Shigella Campylobacter Gonorrhea Mucopurulent conjunctivitis 1. ÷ Usually within several days to weeks Type III hypersensitivity ¡ Classic triad of symptoms: ÷ “Can’t see” Conjunctivitis and/or iritis usually Non-specific urethritis 2. ÷ ÷ “Can’t pee” Discharge and/or dysuria Arthropathy 3. ÷ ÷ “Can’t climb a tree” Involves the lower extremities Triad is found in ~33% cases Acute anterior uveitis occurs in about 5-10% of patients and sometimes becomes chronic. Reactive Arthritis Diagnosis ¡ **HLA-B27 ÷ ¡ ¡ ¡ ¡ ¡ ¡ ¡ ¡ ¡ 65-95% positive Joint X-rays CBC CRP ESR RF ANA Serum creatinine Synovial analysis Culture Treatment ¡ ¡ ¡ ¡ ¡ Spontaneous resolution Anti-inflammatories Antibacterials DMARDs Physical therapy 80-85% of cases resolve w/ no long-term complications ¡ ~15-20% of cases can develop chronic arthritis 3. Ankylosing Spondylitis “inflamed, fused spine” Arthritis of the spinal column ¡ 0.25% prevalence ¡ Chronic and progressive ¡ M > F (3X) ¡ Whites>non-whites ¡ Onset usually 15-35 yo Etiology is unknown ¡ Family history is a risk factor ¡ Possible environmental trigger? Infection? Signs and symptoms ¡ *Chronic pain of the lower spine and buttocks ÷ ÷ ¡ ¡ Sacroillitis Spondylitis Morning stiffness Bamboo spine (fused) ÷ Inflammation à erodes cartilage à allows access to bone and causes bone growth/spurs à bone fusion over time Treatment ¡ *Biologics/TNF inhibitors ¡ Analgesics ¡ Exercise ¡ Anti-inflammatories Anklosing Spondylitis Diagnosis ¡ X-ray of lower spine ¡ Sacroiliac joint is often first affected in AS patients *(+)HLA-B27 ÷ 90+% of patients with AS are HLA-B27 positive Ocular manifestations ¡ ÷ ¡ ¡ ¡ ¡ ¡ Complete blood count (CBC) C-reactive protein (CRP) Erythrocyte sedimentation rate (ESR) (-) Antinuclear antibody (ANA) (-) Rheumatoid factor (RF) *Anterior uveitis affects about 20-40% of patients Usually episodic, unilateral, acute anterior uveitis ÷ Bilateral at some time for 80% of cases ÷ ¡ Consider AS if patient has an acute, recurrent, unilateral anterior uveitis 4. Psoriatic Arthropathy See lecture 29 – Dermatologic Diseases MOA: same as psoriasis except in joints ¡ ¡ 15% of patients will develop arthritis 20-40% are HLA-B27 positive Acute or chronic anterior uveitis may occur in conjunction with psoriatic arthritis ¡ ¡ Not associated with psoriasis without arthritis. 20% of patients will have iritis Diagnosis is based on: ¡ ¡ ¡ Typical dermatological lesions Arthritis of fingers Nail changes Bottom Line: Inflamm. Arthropathies Ocular Manifestations: ¡ ***Uveitis/Iritis*** ¡ *Epi/Scleritis* Quick Summary Slide Spondylarthropathy (+)HLA-B27 Iritis Development Total Combined ~70% 20-40% Crohn’s Disease 50-60% 2.5% Ulcerative Colitis 50-60% 5-10% Reactive Arthritis 60-90% 3-12% *Ankylosing Spondylitis 90-95% 20-40% Psoriatic Arthritis 20-40% 20% Bottom Line: In patients who have iritis and are HLA-B27 positive, there is an underlying spondylarthropathy in 84% of cases! Look further after HLA-B27 testing! Rosenbaum JT. Rheum Dis Clin North Am. 1992;18:143-51. Questions??? Tower 932 [email protected]