Polymyositis and dermatomyositis physical examination: Difference between revisions

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!Percentage
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!Pathognomonic
!Pathognomonic
!highly characteristic
!characteristic
!more common in JDM
!rare in DM
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|Gottron papules
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|Heliotrope rash
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|Eyelids and periorbital tissue  
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|Macular violaceous erythema  
|Macular violaceous erythema  
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|shawl sign
|shawl sign
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|“V sign”
|“V sign”
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|Linear extensor erythema  
|Linear extensor erythema  
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|Mechanic’s hands  
|Mechanic’s hands  
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|Nail abnormalities
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|30-60%
|30-60%
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|Pruritus  
|Pruritus  
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|Sites of compression, such as elbows and buttocks
|Sites of compression, such as elbows and buttocks
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|30-70% in JDM
10% in DM
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|nonscarring alopecia, erythroderma, vesiculobullous lesions,
leukocytoclastic vasculitis, and livedo reticularis
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|Rare
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|30-70%
|10%
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|Flagellate erythema  
|Trunk, back, and proximal extremities
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Revision as of 19:08, 10 April 2018

Polymyositis and dermatomyositis Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Polymyositis and dermatomyositis from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]

Overview

Physical Examination

  • Physical examination of patients with polymyositis and dermatomyositis is usually remarkable for:[finding 1], [finding 2], and [finding 3].
  • The presence of gottron's papules and the heliotrope eruption on physical examination is pathognomonic of dermatomyositis.

Appearance of the Patient

  • Patients with polymyositis and dermatomyositis usually appear normal. They might be weak in severe cases.

Vital Signs

  • Low-grade fever

Skin

  • Skin eruptions like:
    • Gottron's papules is pathognomonic of dermatomyositis.
    • Heliotrope eruption is pathognomonic of dermatomyositis.
    • Gottron's sign
    • Facial erythema
    • Photodistributed poikiloderma
    • Nailfold changes
    • Scalp involvement
    • Calcinosis cutis
    • Mechanic's hands
    • Cutaneous ulceration
  • Skin manifestations of dermatomyositis can be divided into 5 categories:
Lesion Location Picture Percentage Pathognomonic
Gottron papules Dorsal aspect of interphalangeal or metacarpophalangeal joints   80% Pathognomonic
Heliotrope rash Eyelids and periorbital tissue  
Gottron sign   dorsal aspect of the interphalangeal or metacarpophalangeal joints, olecranon process, patella, and medial malleoli   Characteristic
Macular violaceous erythema   Symmetric distribution in classic areas   Characteristic
shawl sign Nape of the neck, shoulders, and upper back   Characteristic
“V sign” V-shaped region of the neck and upper chest   Characteristic
Linear extensor erythema   Extensor aspects of the legs, thighs, arms, fingers, hands, and feet Characteristic
Mechanic’s hands   Palms and fingers   Characteristic
Nail abnormalities nail fold telangiectasias, cuticular overgrowth, and prominent periungual erythema   30-60% Characteristic
Pruritus  
Cutaneous calcinosis   Sites of compression, such as elbows and buttocks 30-70% in JDM

10% in DM

nonscarring alopecia, erythroderma, vesiculobullous lesions,

leukocytoclastic vasculitis, and livedo reticularis

Rare
Flagellate erythema   Trunk, back, and proximal extremities

HEENT

  • Periorbital swelling

Neck

  • Neck examination of patients with polymyositis and dermatomyositis is usually normal.

Lungs

  • Asymmetric chest expansion
  • Lungs are hypo/hyperresonant
  • Fine crackles upon auscultation of the lung bilaterally
  • Wheezing may be present

Heart

  • Cardiovascular examination of patients with polymyositis and dermatomyositis is usually normal.

Abdomen

  • Abdominal examination of patients with polymyositis and dermatomyositis is usually normal.

Back

  • Back examination of patients with polymyositis and dermatomyositis is usually normal.

Genitourinary

  • Genitourinary examination of patients with polymyositis and dermatomyositis is usually normal.

Neuromuscular

  • Patient is usually oriented to persons, place, and time
  • Symmetric proximal muscle weakness mostly in:
    • Deltoids
    • Hips
    • Neck flexors
  • Mild distal muscle weakness
  • Hyporeflexia / areflexia
  • Muscle rigidity

Extremities

  • Muscle atrophy in severe, long standing disease
  • Fasciculations in the upper/lower extremity

References