MSK Flashcards
(39 cards)
chondrolysis
process of rapid cartilage degeneration resulting in narrowing of joint space and loss of motionchondrolysis
-degeneration process associated with infection,trauma, AC:
-hip: SCFE
-females/ adolescence
Diagnosis: signs of joint narrowing, erosions of subchrondral bone, osteopenia
Txt: NSAIDS, protected WB, surgery
what is the most common joint disease
OA
note: 60% men 70% females after age 65
prevalence increase (aging and obesity)
OA
degenrative joint disease, slowly evolving articular disease appear to orginate in cartilage and affect underlying bone, soft tissue, synovial fluid
OA risk factor for CVD
-joint space narrows, osteophytes
S&S
-onset insidious
-pain progress slow
-deep ache worse with activity better after rest
-bony enlargement, crepitus on motion, tender to pressure, joint effusion
-soft tissue inflammation and edema
-joint stiffness <30 mins after inactivity
-morning stiff last 5-10 mins
-movemnt dissipate stiffness
clinical manifestations more:
-OA after menopause
-PIP and DIP affected
-Heberden nodes (DIP)
-Bouchard nodes (PIP)
txt:
shift to psychosocial problems
no cure
what is crepitus and what disease
audible crackling or grating sensation produced whenn roughened articular/extraarticular surfaces rub together during movement
-OA
herberden nodes
DIP
Bouchard nodes affect
PIP
Kellgren and Lawrence grading system for knee
- possible osteophyte; no joint space narrowing
2.definite osteophyte; possible narrowing
- moderate multiple osteophyte;definite joint narrowing; some sclerosis and possible deformity of bone ends
- large osteophytes; marked joint space narrowing; severe scerolsis and definite demority of bone ends
OA
RA
systemic disorders encompassing more than 100 diff diseases
-chronic systemic inflammatory disease that manifests with a wide range of articular and extraarticular findings
-onset of joint pain and loss of function accompained by: fever, rash, diarrhea, sceritis, neuritis by repetitive overuse or trauma
-periods of exacerbation and remission
incidence: 1-2%
second most prevalent after OA
risk factor: age and female
peak onset: 30-60 y/o
women
associated with: graves and hashimoto thyroiditis
etologic factors: unknown but joint inflammation is b/c massive infilitration of T lymphocytes in synovial fluid, genetic predispotion, environmental triggers
-rheumatoid factor-positive (autoantibodies that react w/ immunoglobulin antibodies)
-influx of leukocytes; synovium becomes edematous –> synovitis
-pannus
-dissolves collagen, cartilage
clinical manifestation:
-matrix metalloproteinase –> cartilage destruction, synovial hyperplasia, tender, swell
-elevated cytokines –> osteoclasts increase
-joint instability, joint deformity, anklylosis
-multiple joints, symmetric, bilateral presentation
deformities common: ulnar deviation, swan neck, boutonniere
Soft tissue: synovitis, bursitis, tendinitis, fascitis, neuritis, vasculitis
spine: cervical instability
-C1-C2 sublux , BS/SC compression
-positive lhermitte sign
-babinski sign
-peripheral neuropathy
cutaneous:
-rhumatoid nodule (granulomatous lesions usually occur over extensor surfaces of elbow, achilies tendon, extensor surface of fingers)
-nodulosis
-urinary and fecal incontinence and paralysis
articular findings vs extra articular findings for RA
articular: c**hornic polyarthritis **which perpetuates a gradual destruction of joint tissues, can result in severe deformity and disability
extraarticular: the cardiovascular, pulmonary, and GI system
-eye lesion, infection, and osteoporosis
pannus
RA
destructive vascular grandulation tissue
note: prevents lubrication of joint and nutrients to avascular articular cartilage
flexion deformity at DIP with hyperextension at POP
swan neck
RA
flexion deformity of PIP
bountonniere
greater a person has RA greater likelihood of cervical spine disease
true
note: deep ache cervical pain radiate into occipital, retrooribital, temporal areas
facial and ear pain and occipital HA (C2 irritation nerve)
rheumatoid vasculitis
type of neuropathy
-medium sized arteries to muscles can lead to mononeuritis multiplex
small vessel vasculitis
stocking glove peripheral neuropathy
-small brown infarcts found in palm and digits
juvenile idiopathic arthritis
heterogenous group of arthritdes of unknown cause beg in children up to 18 years of age commonly begin at toddler or early adolescent period and occuring at least 6 weeks
-pain dull and ache and less severe–> in morning during day > night
pauciarticular JIA
-most common
-<4 joints during first 6 months
-assymetric pattern
-girls age 1-5
-LLD
-swollen joint, abnormal gait
polyarticular JIA
->5
-symmetric
-girls
1.rheumatoid factor positive RF+
(prescence of rheumatoid factor)
2. rheumatoid factor negatie (RF-)
not postive
less severe joint involvement
-morning stiff; low grade fever
systemic onset JIA
-any number of joints
-boys=girls
-most severe extraarticular manifestation
-high spiking fever and chills intermittent –> rash
txt: control pain, perserve joint motion
spondyloarthropathies
group of disorders considered variants of RA
-characterized by inflammation of joints in spine
-AS
-sjogren syndrome
-psoriatic arthritis
-reactive arthritis
-reiter syndrome
common features:
-chronic inflammation –> axial skeleton and SI joints
-asymmetric
-young males
-familial predisposition
-inflammation at sites of lig, tendons, fascial insertion into bone
-seronegativity for RF but HLA-B27
-extraarticular involveent of eyes, skin, genitourinary tract, cardiac
ankylosing spondylitis
aka marie strumpell
-inflammatory arthropathy of axial skeleton
-erosive osteopenia and bony overgttowth
-1/3 have asymmetric
-lead to fibrosis, calcification, ossification with fusion of joints
-pain resultant postural deformities, complications can be disabling
-young ppl 15-30 y/o
(backpain 30-65)
-men
**-bamboo spine (fused bones) **
-low back pain ,butt, hip,stiff last at least 3 months
-initial dull ache –> severe constant
-symptoms increase with prolonged rest!!! relieved with active movement
-radiate to thigh
-morning stiff > 1 hr
-enthesitis
-loss of lumbar lordosis increase kyphosis of thoracic spine
complications:
-osteoporosis, fracture, AA sublux, spinal stenosis
-IBS, weight loss
-uveitis
txt:
-control inflammation and stiff
-maintain mobility
-educate
-lifestyle modification
-periods of exacerbation and remission
enthesis
chronic nongranulamatous inflammation at area where ligaments attach to vertebrae
-AS
enthesitis
inflammation of tendons, ligaments, capsular attachments to bone
-AS
DISH
diffuse idiopathic skeletal hyperotosis
-idiopathic variant of OA
-forestier disease
-ossifcation of longitudinal ligaments
-thoracic spine most affected
-men 50-70 y/o
-contrast to OA: DISH does not directly result in degeneration of vertebral facet joints; joint space narrowing, spondylophytes INSTEAD manifest with** syndesmophytes **
clinical manifestion
-asymptomatic early
-dull pain and stiff prolonged rest or with spinal bending or twisting
-subsite with rest and NSAIDS
-extensive hyperostosis formation along anterior cervical spine (horaseness, stridor,dysphasia)
-vertebral fracture of cervical or thoracic
what are syndesmophytes
bony outgrowths attached to ligaments
-DISH
leads to decrease mobility esp lumbar spine
DISH vs AS
DISH:
-older 50-70
-cervical thoracic>lumbar
-no SI involved
-loosely ossification
sjogren syndrome
chronic autoimmune disease that cause athritis effects in several organs
-commonly the moisture producing glands(mouth, eyes) but also joints, lungs, kidney
-second most common autoimmune rheumatic disease
-women
**HALLMARK: dry eyes and dry mouth **
-keratoconjunctivits sicca
-xerostomia (dry mouth) and dry cough
clinical manifestations:
-dry throat, esophagitis, gastritis, dental cavities from lack of salivia
-raynaud pheunomenon, b cell lymphoma, inflammation of lungs, kidney disease
-depression,anxiety,thyroditis, fibromyalgia
-QOL decrease