MSK Dx Flashcards
{{BLANK}} myopathy is assoc. w/ serum CK elevations and rhabdomyolysis
Hypothyroid
{{BLANK}} myopathy is assoc. w/ myofiber necrosis & regeneration
Histologic findings
Thyrotoxic myopathy
{{BLANK}} is a potent vasoconstrictor that can lead to diffuse ischemia & rhabdomyolysis
Direct effects on myocytes –> Rhabdomyolysis
Cocaine
Statins can inhibit the synthesis of {{BLANK}} which plays a key role in muscle cell energy production
CoQ10
{{BLANK}} is a direct mitochondrial toxin & can cause rhabdomyolysis & ARF secondary to myoglobinuria
Also: Electrolyte abnormalities – phosphate, K, Mg, Ca
EtOH Myopathy
What is the Rhabdo triad?
- Myalgia
- Generalized weakness
- tea-colored urine (myoglobin)
What is displayed in the histopathology slide attached? What disease does this patient likely have?
- Ragged Red Fibers
- MERRF
{{BLANK}} is due to a point mutation in mit-DNA leading to generalized seizures, cerebellar ataxia, and dementia.
Destruction of oxidative phosphorylation proteins
MERRF
{{BLANK}} is due to maternally inherited mit-DNA mutations that result in muscle weakness and tonic-clonic seizures
MELAS (encephalomyopathy, lactic acidosis, and stroke-like episodes)
{{BLANK}} has the hallmark S/Sx of the inability to relax voluntary muscle after contraction
Myotonic dystrophy
Myotonic dystrophy displays {{BLANK}} as the risk increases with progeny
Anticipation; CTG repeats
Most myotonic dystrophy cases are due to a defective {{BLANK}} enzyme
DMPK
Prefentially, {{BLANK}}-muscle fibers are affected in myotonic dystrophy
Type I (slow-twitch)
DMD and BMD both result in deleted dystrophin but {{BLANK}} is worse and more aggressive
DMD
Inclusion body myositis is most severe in the muscles: {{BLANK}} and {{BLANK}}
- Quadriceps
- UE muscles