FINAL EXAM Flashcards
arthritis that causes P, swelling, tenderness & redness at joint, often big toe
– inflammatory arthritis caused by crystallization of uric acid inside a joint forming a tophi or tophus surrounding joint
– tophus = deposit of monosodium urate crystals with macrophages & lymphocytes
gout
90% affected individuals experience acute attacks in following locations:
-1st MTP joint (big toe), carpal joints, ankles, heels
-knees, wrists, elbows
-fingers
symptoms include: intense joint P, swelling or inflammation & redness, limited ROM, lingering discomfort, fever, chills, headache or nausea, kidney stones or kidney failure may also occur
gout
autoimmune disease that causes abnormal response to synovial cells in synovium of some synovial joints to attack themselves as if they were a foreign invader
– symmetrical polyarticular arthritis, mostly in small joints
– weakness, fever, malaise joint P
– morning stiffness common
rheumatoid arthritis
5 stages of rheumatoid arthritis
Stage 1: Synovitis
Stage 2: Pannus formation
Stage 3: Cartilage erosion
Stage 4: Fibrosis
Stage 5: Ankylosis
chronic arthritis that affects people with psoriasis 20-30% of time, skin condition & joints
– red patches of skin with silvery scales & also may affect nails
psoriatic arthritis
pain, stiffness & swelling = most common symptoms often in hands & feet, can be anywhere in body
– symptoms range from mild to severe, alternating periods of exacerbation & remission
– destruction & deformity of joints of hands & feet, causing “sausage finger” & loss of mobility of IP joints
– asymmetrical
psoriatic arthritis
degeneration of a joints articular cartilage along high stress lines that causes inflammation
osteoarthritis
joint pain with crepitus
– slow, continual progression over years & decades, joints slowly deteriorate over time
– morning stiffness (<30 minutes) improves
– little inflammation, some swelling
– loss of flexibility
– major weight bearing joints affected: knees & hips with lesser involvement in SH
– Heberden’s nodes commonly found at DIP joints in women
osteoarthritis
joint stiffness, swelling & P triggered by bacterial infection
– P felt in lower back, ankles, knees, feet & IP joints
– enthesitis common
– eye & urinary symptoms present in chlamydia infection
– strongly associated with HLA-B27 gene mutation & more common in men
– if involves eyes (uveitis) & follows a chlamydia (urethritis) infection = Reiter’s Syndrome
reactive arthritis
imbalance between bone deposition (bone making) & bone decomposition (bone break down) causing bone tissue to become “porous”
osteoporosis
– pain & disability due to fractures, common sites are vertebral body, hip & wrists
– vertebral bodies compressed causing loss of height & if in thoracic spine, causes kyphosis
– common in aging population especially post menopausal women
osteoporosis
– advanced age, cerebrovascular disease (Alzheimer’s disease caused by damage to brain tissue & vascular dementia caused by damage to blood vessels)
– CNS infections, brain trauma/tumours, vitamin deficiencies, metabolic, endocrine conditions, chronic alcoholism, long-term exposure to aluminum & other metals, multiple sclerosis, syphilis
– Huntington’s disease, Parkinson’s disease & immune disorders such as acquired immunodeficiency syndrome (AIDS
dementia
– unknown, associated with advancing age, genetics factors present in 5-10% of cases
– causes abnormal protein clumps called plaques & irregular knots called neurofibrillary tangles to form in nerve cells in brain
Alzheimer’s
quadriplegia causes
cervical spine injury, paralysis of trunk & all extremities, including pelvic organs
paraplegia causes
lower thoracic or lumbar spine injury, paralysis of lower trunk & legs, including pelvic organs
causes of Parkinson’s (primary & secondary)
primary: unknown possibly genetic
secondary: may be by infection, trauma, tumour, atherosclerosis or drug use
minor stretch & tear, no joint instability on passive testing, minimal P & swelling, able to complete ADLs with minor discomfort, can weight bear, bruising absent/ slight
grade 1 sprain
extensive damage to fibers or tendon, but mm not completely ruptured, snapping sound may or may not be present, can sometimes feel gap at injury site, edema, P (moderate) tenderness at site, difficulty with ADLs, loss of strength, heals in 3 – 6 weeks
grade 2 strain
urinary tract infection: often E. coli microorganisms (fecal) enter lower urinary tract & ascend upwards through ureter to kidney
– bacteria may travel to kidneys via bloodstream, causes kidneys to swell & may damage them permanently
– associated with kidney stones, pregnancy, medical instrument contamination (catheter, cystoscope), female sexual trauma & men with (benign prostatic hypertrophy BPH)
acute pyelonephritis
escherichia coli bacterial infection most common, 2nd schistosomiasis, these microorganisms ascend through urethra, other microorganisms may enter via bloodstream
urinary tract infection (UTI)
– most commonly complications from streptococcus infection, antibodies produced against strain, then clump up & lodge inside glomerulus causing inflammation, sometimes idiopathic
– other causes: virus (hepatitis B,C, HIV), diabetes, hypertension, lupus
glomerulonephritis
variable in region & intensity, tall stature, thin long extremities, protruding breastbone, crowded teeth, heart murmurs, extreme nearsightedness, curved spine & flat feet
– symptoms may be mild or severe, if affecting aorta, may be life threatening & require surgery
Marfan’s syndrome
– copper accumulates in liver & brain or other organs causing liver disease, neuropsychiatric symptoms or other
– copper can accumulate in eyes called Kayser-Fleischer ring which is a brown ring at edge of iris
– common symptoms include fatigue, lack of appetite, abdominal pain, yellow skin, speech or swallowing difficulty & mm stiffness
Wilson’s disease
– persistent urge to urinate, burning sensation, frequent small amounts of urination, blood in urine (hematuria), cloudy strong smelling urine, pelvic discomfort, pressure & low fever, may spread upwards through ureters to kidneys
cystitis
– aching, burning, or cramping pain in specific area in an extremity
– feels tight with numbness & tingling, weakness, worsens with exercise
compartment syndrome
often triggered by something else
– most common symptoms are pain; aching, burning or gnawing, insomnia, visual problems, memory & mood disorders, cognitive disorders, fatigue,morning stiffness – P begins in localized area: neck & shoulders, becomes more generalized
– often linked to headaches, TMJ disorders, IBS, Crohn’s or ulcerative colitis, anxiety & depression
– sufferers state they are in pain 90% of their waking hours
fibromyalgia
tightness of skin of face give it a “mask-like” appearance
– mouth may not open or close completely
– hands appear red, pale & swollen, fingers become tapered and flexed
– skin appears hard, shiny & stretched
– weakness & fatigue also common symptoms
scleroderma
may go deeper & affect internal organs like heart & cause arrhythmias or respiratory failure, renal failure, esophageal or intestinal blockage or perforation and damage to vascular walls (causing Raynaud’s phenomenon) → blood flow to fingers & toes is extremely reduced by vasospasm causing discoloration
scleroderma
mm atrophy & wasting, mm weakness, lack of coordination, progressive deformity with physical & cognitive (5% of time) disability
– child has waddling gait, difficulty climbing stairs or running, falls easily
– child uses arms to push off to rise from sitting to standing, called “Gower’s Sign” → may affect heart and respiratory system which may be fatal
– most deaths occur from respiratory complications
muscular dystrophy
2 types of spina bifida
spina bifida occulta: hidden, mildest & most common, one or more SPs fail to unite leaving open gap posteriorly
myelomeningocele: most severe, SP’s fail to form at multiple locations (usually L-spine) & spinal canal is open exposing meninges, spinal cord & nerves, other tissues – life threatening, also may cause paralysis
meningocele: very rare, just meninges herniate, no cord involvement