Exam 5: Musculoskeletal Pathologies Flashcards
osteoarthritis
- older ppl or athletes
- breakdown of articular cartilage
- exacerbated by use
RA
- autoimmune
- small joints
- joints warm / painful / stiff w/ inactivity
- symmetric
ulnar deviation of metacarpophalangeal joints
HANDS
RA - histologically
synovium thickened, hyperplastic, lots of lymphoid aggregates
gout
excessive uric acid
BIG TOE with TOPHI
gout risk factors
age duration of hyperuricemia heavy ALCOHOL obesity drugs (thiazides) lead toxicity
tophi
- urate crystals with inflammation
- NEEDLE LIKE
pseudogout
- calcium phosphate
- hereditary
- RHOMBOID / GEOMETRIC crystals
bacteria that can cause infectious arthritis
- TB
- lyme: borrelia burgdorferi
- gonococcus
- staph aureus
- influenza
- salmonella
viruses that can cause infectious arthritis
parvovirus
rubella
HCV
what kind of patients are associated with salmonella?
sickle cell patients
type 1 muscle fiber
- slow twitch
- weight bearing
- mitochondrial / ox phos pathway
- lipid metabolism
type 2 muscle fiber
- fast twitch
- purposeful movement
- glycogen metabolism
denervation atrophy - histologically
- angular, atrophic
- mm shrinks, nuclei remain on outside and look like giant cells
- target fibers
type grouping
- after denervation, the nerve closest to the muscles re-enervates them
- it’s when you see ONE type of mm fibers - lack of checkerboard pattern
amylotrophic lateral sclerosis
- 60 years old, M>F
- muscular atrophy
- hand weakness (early)
- progressive + respiratory mm weakness (late)
ALS death due to
respiratory failure
bronchopneumonia
ALS macroscopic findings
- shrunken / atrophic anterior nerve roots
- distal > proximal
ALS microscopic findings
- bunina inclusion bodies
- degeneration of myelinated fibers in the corticospinal tracts
a denervation injury always looks like this histologically
angulated, atrophic fibers
a myopathy always looks like this histologically
- rounded atrophic fibers
- vacuoles
- degeneration, regeneration, fibrosis
2 mutations of dystrophin gene
Duchenne MD,
Becker MD
duchenne MD
- dystrophinopathy
- dystrophin ABSENT
- no brown
becker MD
dystrophine reduced
- some brown
dystrophinopathies - clinically
- proximal weakness
- calf pseudo-hypertrophy
- CK elevated early
- death from respiratory, cardiac failure
polymyositis
- an inflammatory myopathy
- infiltrate can be aggressive
- becomes necrotic post infiltration
dermatomyositis
- facial rash
- perifascicular atrophy
McArdle’s Disease
- glycogen defect
- myophosphorylase deficiency
- PAS stain +
Carnitine Palmityl Transferase Deficiency
- lipid defect
- Oil red O stains red
mitochondrial myopathies
- proximal weakness
- opthalmoplegia
drug induced myopathies can be caused by
- steroids
- statin drugs
- colchicine
- ethanol
malignant hyperthermia
- an ion channel myopathy
- hypermetabolic state
- trigger: ANESTHESIA
- gene mutation in Ca channel (RYR1)
Myasthenia gravis
- loss of Ach receptors
- post synaptic
- thymus problems
- worsened by exercise
- ptosis
Lambert Eaton Syndrome
- ppl with small cell lung cancer
- presynaptic
- Ab to presynaptic voltage gated Ca channels