Musculoskeletal Diseases and Disorders

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    Musculoskeletal Diseases and

    Disorders

    Arif Pandega,MD

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    Musculoskeletal System Bones

    Long, short, flat, irregular

    Compact, spongy

    Joints

    Bursae

    Muscles Tendons

    Ligaments

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    Disorders of Bone Spinal deformities

    Herniated intervertebral discsOsteoporosis

    Osteomyelitis

    Pagets Disease (osteitis deformans) Fractures

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    Spinal DeformitiesLordosis

    Abnormal inward or anterior curvature

    Accentuation of normal curve of lumbar spine

    Frequently gradual onset

    Affects lumbar spine

    Also called swayback

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    Spinal DeformitiesEtiologies

    Posture, leg length differences, congenital, epiphyseal

    growth disturbance, trauma, tumors, infection, arthritis,

    TB, endocrine abn, aging

    S/S: usually backache, fatigue, abnormal

    appearance or fitting of clothes

    Treatment: PT, exercise, braces, surgery, pain

    relief

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    Herniated Intervertebral DiscsDisc Anatomy

    Annulus fibrosis

    Nucleus pulposis

    Herniation

    Nucleus pulposis pushes through annulus into spinal

    canalRupture

    Pieces of the disc are free in the spinal canal

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    OsteoporosisMetabolic disorder of bones

    Less bone mineral (calcium) than normal

    Over 10 million in US affected

    Post-menopausal females most commonly

    Bones are brittle, porous, easily brokenMore prone to pathological fracture

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    OsteoporosisEtiology:

    Genetics, calcium intake & dietary, sedentary lifestyle,

    estrogen, vit D, or adrenal deficiency, steroid use,

    alcoholism, etc

    S/S: often asymptomatic until pathological fx.

    Treatment: calcium supplements, meds(antiresorptive, restorative of lost bone, etc)

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    OsteomyelitisAcute or chronic bone infection

    Inflammation, edema, circulatory problems

    More common in children

    Etiology:

    Trauma most commonly with bacterial invasion from

    the skin Infection may also spread from adjacent tissues or

    blood supply

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    OsteomyelitisRisk factors:

    Diabetes, orthopedic hardware, splenectomy & SSA,

    hemodialysis, IV drug users

    S/S: may be asymptomatic for years

    Treatment:

    Long-term antibiotics, sometimes surgical debridement

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    Pagets DiseaseOsteitis Deformans

    Chronic metabolic bone disease

    High rate of bone turnover (reabsorption & deposition)

    Thicker but softer bone is the result

    Patients typically over 40 YOAOne or many bones

    Usually lower torse involve

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    Pagets DiseaseEtiology: Unknown

    S/S: graduation onset of swelling & pain

    Treatment:

    PT, pain management, surgery

    Medications (biphosphonates or calcitonin)

    Joint replacements

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    Fractures Closed/simple

    Open/compound

    Greenstick

    Displaced

    Comminuted

    Segmental

    Spiral

    Pathological

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    Pathology Part 2

    Types of fractures

    Complex Incomplete Comminuted Greenstick

    Simple (closed) Compound (open) Colles Impacted

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    OsteoarthritisMost common form of arthritis

    Chronic inflammation causing degeneration and

    new bone formation

    Weight-bearing joints most common

    Knees, hips

    Common in older patients (over 55 YOA)

    In over 70 YOA, females more frequently affected

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    Rheumatoid ArthritisChronic, systemic, polyarticular inflammatioy

    disease

    Destruction (erosion) of bone & cartilage

    Causes ankylosis (fibrous fusion of joints, immobile)

    Exacerbations and remissions unpredictable

    Affects mostly females

    Increasing risk with advancing age

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    Rheumatoid Arthritis (RA)Etiology: autoimmune, genetics

    S/S: symmetric pain, swelling of hands & fingers,

    also other LE joints, systemic (fever, fatigue, wt.Loss)

    Dx testing: Rheumatoid factor blood test

    Treatment:Antiinflammatories, PT, antimetabolites, antirheumatic

    drugs

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    GoutGouty arthritis

    Chronic uric acid metabolism disorder

    Uric acid crystals deposited in joints

    Tophi formation (urate compounds) around joints

    Acute, severe episodes of arthritis

    Mostly male patientsOther associated problems:

    Kidney stones, renal failure, hyperuricemia

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    GoutEtiology:

    Metabolic, renal, some genetics

    S/S:Severe signs & symptoms of inflammation

    Big toe is classical site

    Treatment:Pain relief, antiinflammatories, colchicine, diet low in

    purines, alopurinol

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    Muscles & Connective Tissue

    Diseases Sprains & strains

    Bursitis & tendonitis

    Carpal Tunnel Syndrome

    Myasthenia Gravis (MG)

    Polymyositis Systemic Lupus Erythematosus (SLE)

    Duchennes Muscular Dystrophy

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    Sprains & Strains Sprain

    Ligamentous tearing/stretching after a tortion injury

    Strain

    Tearing/stretching of tendon or muscle

    Etiology: trauma or overuse

    S/S: localized pain, swelling, limitation of motion

    Treatment: supportive, pain relief

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    Bursitis & TendonitisBursitis

    Inflammation of fluid-filled bursae near joints

    Shoulder, hip, elbow, knee

    Tendonitis

    Inflammation of tendon or tendon-muscle attachement

    Shoulder, wrist, Achilles, hamstringEtiology: trauma, excessive use, other diseases

    S/S: pain, swelling, LOM, fluid accumulation

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    Bursitis & TendonitisTreatment

    Varies with anatomic location & degree of disability

    Anti-inflammatories & pain relievers, splinting,

    exercise, orthotics, steroid injections, PT

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    Carpal Tunnel SyndromeCompression of median nerve within the carpal

    tunnel of the wrist

    Common syndrome with repetitive use work

    Involves pain, sensory & motor symptoms

    Etiology: edema within the carpal tunnel, causing

    inflammation of the nerve & other structures there

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    Carpal Tunnel Syndrome S/S:

    Wrist pain, burning or tingling paresthesias, numbness

    Weakness of hand grasp

    Tinels sign

    Treatment:

    Wrist immobilization, anti-inflammatories

    Rarely surgery

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    Myasthenia GravisRare, autoimmune disorder of the neuromuscular

    junction

    Antibodies against the acetylcholine receptors

    (post-synaptic)

    Chronic, progressive disease causing sporadic

    weakness of the skeletal muscles

    Most common in females, ages 20-40 YOA

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    Myasthenia Gravis (MG)Reduced muscle strength & longer recovery time

    with repeated use

    Symptoms late in the day

    Bulbar (eye & facial) muscles involved first

    Facial expression, drooping lids, etc.

    Thymomas in 15% MG patients

    75% have some thymic abnormality (hyperplasia)

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    MGDiagnostic testing:

    Tensilon test (edrophonium challenge will increase

    muscle strength)Treatment:

    Oral anticholinergic meds (pyridostigmine,neostigmine), immune suppressives, cholinesteraseinhibitors like edrophonium

    Prognosis: normal life expectancy in moderntimes

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    PolymyositisChronic, idiopathic inflammatory disease of

    connective tissues and muscles

    Exacerbations & remissions

    May have skin involvement (dermatomyositis)

    females more than males

    Bimodal peak of onset: 5-15 YOA & 50-70YOA

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    Polymyositis S/S: sudden or slow weakness of muscle group over

    weeks to months

    Often have trouble arising from sitting or raising arms abovehead, also voice changes

    Fever, fatigue, weight loss

    Skin: lilac-colored rash of eyelids, nose and face

    Dx via EMG & muscle biopsy

    Treatment: immune suppressive

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    Systemic Lupus ErythematosusLupus or SLE

    Multisystem, autoimmune, inflammatory disease

    due to antibodies against cell nuclei

    Females outnumber male patients ( 9 to 1)

    Genetics may also be involved

    Arthralgias are first complaint in most patients

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    SLEOrgan involvement:

    Skin, renal, CNS, GI, blood, musculoskeletal, CV,

    pulmonary, vascular endothelium (Raynauds)

    Four criteria at any time:

    Malar rash or discoid rash, photosensitivity, arthritis,

    renal disease, neuro, skin, hematologic, or immunedisorders, +ANA blood test

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    SLETreatment:

    Anti-inflammatories, pain relief, immune suppressives

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    Duchennes Muscular Dystrophy Inherited, x-linked, recessive disorder

    Seen only in males

    Occasionally no family history

    Rapidly progressive wasting of skeletal muscles

    First in lower extremity & pelvis, then generalizes

    Usually appears by 6 YOACause of death: respiratory insufficiency usually

    by 25 YOA

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    Duchennes Muscular DystrophyAt first muscles appear larger

    Due to fat and CT infiltration

    Then atrophy (wasting, decrease in size)

    Then scarring & contractures

    Cardiomyopathy present in almost all cases

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    NeoplasmsOsteogenic sarcoma

    Chondrosarcoma

    Malignant giant-cell tumor

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    Osteogenic SarcomaMost common bone cancer

    3rdmost common cancer in adolescence

    Slightly more males

    Risk factors: radiation therapy, genetics

    Treatment: surgical, but mets later in 80%Most in long bones

    Femur, tibia, humerus (in that order)

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    Chondrosarcoma 2ndmost frequent primary bone cancer (25%)

    Malignant tumor of cartilage

    Mostly over 40 YOA (mostly geriatric)

    Affects pelvis, femur, humerus, ribs

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