Polymyositis and dermatomyositis physical examination
Polymyositis and dermatomyositis Microchapters |
Differentiating Polymyositis and dermatomyositis from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Polymyositis and dermatomyositis physical examination On the Web |
American Roentgen Ray Society Images of Polymyositis and dermatomyositis physical examination |
FDA on Polymyositis and dermatomyositis physical examination |
CDC on Polymyositis and dermatomyositis physical examination |
Polymyositis and dermatomyositis physical examination in the news |
Blogs on Polymyositis and dermatomyositis physical examination |
Risk calculators and risk factors for Polymyositis and dermatomyositis physical examination |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]
Overview
Physical examination of patients with polymyositis and dermatomyositis is usually remarkable for muscle weakness, hyporeflexia, skin lesions, respiratory symptoms. The presence of Gottron's papules and the heliotrope eruption on physical examination is pathognomonic of dermatomyositis. Muscle atrophy in severe, long standing disease might occur.
Physical Examination
- Physical examination of patients with polymyositis and dermatomyositis is usually remarkable for muscle weakness, hyporeflexia, skin lesions, respiratory symptoms.[1][2][3][4][5]
- 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
Lesion | Location | Percentage | Pathognomonic |
---|---|---|---|
Gottron papules | Dorsal aspect of interphalangeal or metacarpophalangeal joints | 80% | Pathognomonic |
Heliotrope rash | Eyelids and periorbital tissue | Pathognomonic | |
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 such as
|
Nail of hands and feet | 30-60% | Characteristic |
Cutaneous calcinosis | Sites of compression, such as elbows and buttocks | 30-70% in JDM
10% in DM |
|
Flagellate erythema | Trunk, back, and proximal extremities | Rare | |
Poikiloderma | Sun exposed areas | Rare | |
Pityriasis rubra pilaris–like lesions | dorsal aspect of the hands and feet, frequently over the bony prominences | Rare | |
Nonscarring alopecia | Head | Rare | |
Erythroderma | Rare | ||
Vesiculobullous lesions | Rare | ||
Cutaneous vasculitis such as
|
Rare | ||
Leukocytoclastic vasculitis | Underlying malignancy | Rare | |
Raynaud phenomenon | 25% |
HEENT
Neck
- Neck examination of patients with polymyositis and dermatomyositis is usually normal.
Lungs
- Asymmetric chest expansion
- Lungs are hyporesonant
- 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:
- Mild distal muscle weakness
Extremities
- Muscle atrophy in severe, long standing disease
- Fasciculations in the upper/lower extremity
References
- ↑ 1.0 1.1 Khan, Sabiha; Christopher-Stine, Lisa (2011). "Polymyositis, Dermatomyositis, and Autoimmune Necrotizing Myopathy: Clinical Features". Rheumatic Disease Clinics of North America. 37 (2): 143–158. doi:10.1016/j.rdc.2011.01.001. ISSN 0889-857X.
- ↑ Dobloug, Cecilie; Garen, Torhild; Bitter, Helle; Stjärne, Johan; Stenseth, Guri; Grøvle, Lars; Sem, Marthe; Gran, Jan Tore; Molberg, Øyvind (2015). "Prevalence and clinical characteristics of adult polymyositis and dermatomyositis; data from a large and unselected Norwegian cohort". Annals of the Rheumatic Diseases. 74 (8): 1551–1556. doi:10.1136/annrheumdis-2013-205127. ISSN 0003-4967.
- ↑ Chinoy, H.; Fertig, N.; Oddis, C. V; Ollier, W. E R; Cooper, R. G (2007). "The diagnostic utility of myositis autoantibody testing for predicting the risk of cancer-associated myositis". Annals of the Rheumatic Diseases. 66 (10): 1345–1349. doi:10.1136/ard.2006.068502. ISSN 0003-4967.
- ↑ Dalakas, Marinos C; Hohlfeld, Reinhard (2003). "Polymyositis and dermatomyositis". The Lancet. 362 (9388): 971–982. doi:10.1016/S0140-6736(03)14368-1. ISSN 0140-6736.
- ↑ Douglas, William W.; Tazelaar, Henry D.; Hartman, Thomas E.; Hartman, Robert P.; Decker, Paul A.; Schroeder, Darrell R.; Ryu, Jay H. (2001). "Polymyositis–Dermatomyositis-associated Interstitial Lung Disease". American Journal of Respiratory and Critical Care Medicine. 164 (7): 1182–1185. doi:10.1164/ajrccm.164.7.2103110. ISSN 1073-449X.