INFLAMMATORY MUSCLE DISEASE Flashcards

1
Q

INFLAMMATORY MUSCLE DISEASE
🌸 TYPES

A

⭐ POLYMYOSITIS
⭐ DERMATOMYOSITIS
⭐ JUVENILE DERMATOMYOSITIS
⭐ INCLUSION BODY MYOSITIS
⭐ IMMUNE MEDIATED NECROTISING MYOPATHY
⭐ CANCER ASSOCIATED MYOPATHY
⭐ ANTI-SYNTHETASE Syndrome
⭐ Amyopathic DERMATOMYOSITIS

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2
Q

PAINLESS

PROGRESSIVE

SYMMETRICAL

LOWER LIMB PREDOMINANT

PERSISTANT SUBACUTE PROXIMAL WEAKNESS

A

Inflammatory MYOPATHIES

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3
Q

Muscle Involvement in INFLAMMATORY MUSCLE DISEASE

A
  1. Pharyngeal
    ⬇️
  2. Esophageal
    ⬇️
  3. Neck Flexors
    ⬇️
  4. Respiratory Muscles
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4
Q

GOLD STANDARD INVESTIGATION FOR INFLAMMATORY MUSCLE DISEASE

A

Muscle BIOPSY

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5
Q

Investigation in INFLAMMATORY MUSCLE DISEASE

A
  1. Muscle Biopsy
  2. CPK ⬆️
  3. Aldolase B
  4. EMG
  5. MRI of Thigh Muscle
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6
Q

Age group: Juvenile DERMATOMYOSITIS

Age group: Adult onset DERMATOMYOSITIS

A

⭐ 5-15 yrs

⭐ 45-65 yrs

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7
Q

F:M in DERMATOMYOSITIS

A

2:1

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8
Q

Skin lesion in Dermatomyositis occurs by

A

6 months BEFORE Weakness

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9
Q

Weakness does not occur by 6 months of Skin lesions is known as

A

AMYOPATHIC DERMATOMYOSITIS

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10
Q

Acute PRESENTATION of DERMATOMYOSITIS

A

Pain and Weakness for Weeks to Months
In 30% pts

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11
Q

Difference between Gottron’s papules and Gottron’s Rash

A

Anything other than a papules in place of Gottron’s papules

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12
Q

Calcinosis Cutis seen in

A
  1. Systemic Sclerosis
  2. Juvenile DERMATOMYOSITIS
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13
Q

Pathognomic SIGNS in DERMATOMYOSITIS

A
  1. Gottron papules
  2. Heliotrope Rash
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14
Q

Signs seen in DERMATOMYOSITIS
Less-SPECIFIC

A
  1. Gottron’s sign
  2. Photo sensitivity
  3. V sign
  4. Shawl sign
  5. Holster sign
  6. Nail fold capillary changes with cuticular overgrowth
  7. Pruritic Scalp Involvement
  8. Mechanic Hand
  9. Calcinosis cutis
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15
Q

EMG in INFLAMMATORY MUSCLE DISEASE

A

⭐ Polyphasic Short Duration Small Amplitude Potentials

⭐ High frequency discharges

⭐ Spontaneous activity like fibrillation or Denervation

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16
Q

Classical FINDING in DERMATOMYOSITIS

A

Peri-vascular lymphocytic infiltrates

Peri-Fasicular Atrophy

No NECROSIS

17
Q

In Juvenile DERMATOMYOSITIS always rule out

A

Malignancy of Ovary and Lung

18
Q

DERMATOMYOSITIS like weakness ⛔ Skin lesion

Late Presentation 50-60yrs

Necrosis ➕ at BIOPSY (But NO ATROPHY)

A

POLYMYOSITIS

19
Q

Antibodies seen in DERMATOMYOSITIS and POLYMYOSITIS

A

⭐ anti Jo1 (anti-synthetase)

20
Q

Anti-Jo1 ➕ INCREASR THE RISK OF
(Anti-Synthetase)

A
  1. Mechanic’s HAND
  2. Interstitial LUNG Disease: NSIP
  3. Raynaud’s phenomena
  4. Arthritis: SLE-like
21
Q

Which SKIN MANIFESTATION is seen in Both POLYMYOSITIS and DERMATOMYOSITIS

A

Mechanic’s Hand

22
Q

Anti-Mi2
Seen in

A

DERMATOMYOSITIS without ILD
GOOD PROGNOSIS

23
Q

Anti-SRP is ASSOCIATED with

A

Immune-mediated Necrotizing MYOPATHY

ASSOCIATED with statin use

24
Q

Antibody that indicates
✨ RAPID SKIN Involvement
✨ ILD

A

Anti MDA5

25
Q

Antibodies ASSOCIATED with

⭐ Cancer associated DERMATOMYOSITIS
⭐ Juvenile DERMATOMYOSITIS

A

Anti-TIF 1GAMMA
Anti-NxP2 (anti nuclear matrix protein 2)