MSK Dx Flashcards

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1
Q

{{BLANK}} myopathy is assoc. w/ serum CK elevations and rhabdomyolysis

A

Hypothyroid

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2
Q

{{BLANK}} myopathy is assoc. w/ myofiber necrosis & regeneration

Histologic findings

A

Thyrotoxic myopathy

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3
Q

{{BLANK}} is a potent vasoconstrictor that can lead to diffuse ischemia & rhabdomyolysis

Direct effects on myocytes –> Rhabdomyolysis

A

Cocaine

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4
Q

Statins can inhibit the synthesis of {{BLANK}} which plays a key role in muscle cell energy production

A

CoQ10

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5
Q

{{BLANK}} is a direct mitochondrial toxin & can cause rhabdomyolysis & ARF secondary to myoglobinuria

Also: Electrolyte abnormalities – phosphate, K, Mg, Ca

A

EtOH Myopathy

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6
Q

What is the Rhabdo triad?

A
  • Myalgia
  • Generalized weakness
  • tea-colored urine (myoglobin)
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7
Q

What is displayed in the histopathology slide attached? What disease does this patient likely have?

A
  • Ragged Red Fibers
  • MERRF
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8
Q

{{BLANK}} is due to a point mutation in mit-DNA leading to generalized seizures, cerebellar ataxia, and dementia.

Destruction of oxidative phosphorylation proteins

A

MERRF

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9
Q

{{BLANK}} is due to maternally inherited mit-DNA mutations that result in muscle weakness and tonic-clonic seizures

A

MELAS (encephalomyopathy, lactic acidosis, and stroke-like episodes)

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10
Q

{{BLANK}} has the hallmark S/Sx of the inability to relax voluntary muscle after contraction

A

Myotonic dystrophy

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11
Q

Myotonic dystrophy displays {{BLANK}} as the risk increases with progeny

A

Anticipation; CTG repeats

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12
Q

Most myotonic dystrophy cases are due to a defective {{BLANK}} enzyme

A

DMPK

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13
Q

Prefentially, {{BLANK}}-muscle fibers are affected in myotonic dystrophy

A

Type I (slow-twitch)

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14
Q

DMD and BMD both result in deleted dystrophin but {{BLANK}} is worse and more aggressive

A

DMD

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15
Q

Inclusion body myositis is most severe in the muscles: {{BLANK}} and {{BLANK}}

A
  • Quadriceps
  • UE muscles
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16
Q

A 67 yo man comes in complaining of weakness when lifting his grandchild and their right leg when rising from their desk char. The patient also has been experiences difficulty swallowing their morning meds. Attached is the histopathology sample you gathered from their quadriceps. What do you suspect?

A

Inclusion body myositis

Asymmetric weakness of UE & quads w/ inclusion bodies

17
Q

C&C polymyositis with dermatomyositis

A
  • Polymyositis: Endomysial; CD8+ T cells; Adults; No skin
  • Dermatomyositis: Permysial; CD4+ T cells; children & adults; skin

Tx w corticosteroids & immunosuppressants; both ANA & Anti-Jo1

18
Q

Screen for a paraneoplastic syndrome in which areas if you find dermatomyositis?

A

SLOB
* Stomach
* Lung
* Ovaries
* Breast

Remember: Skin manifestations (Heliotrope rash, gottron papules)