Dermatomyositis/polymyositis
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Basics
Description
- Dermatomyositis (DM) and polymyositis (PM) are systemic inflammatory myopathies, which represent the largest group of acquired and potentially treatable causes of skeletal muscle weakness
- Patients experience a marked progression of muscle weakness over weeks to months
- Can lead to respiratory insufficiency from respiratory muscle weakness
- Aspiration pneumonia can occur owing to a weak cough mechanism, pharyngeal muscle dysfunction, and esophageal dysmotility
- Cardiac manifestations include myocarditis, conduction defects, cardiomyopathy, and congestive heart failure (CHF)
- Arthralgias of the hands, wrists, knees, and shoulders with distinct associated skin findings for DM
- Ocular muscles are not involved but facial muscle weakness may be seen in advanced cases
Etiology
- The exact cause is unknown, although autoimmune mechanisms are thought to be largely responsible
- Incidence ∼2:100,000 with a female preponderance
- There may be an association between PM and certain viral, bacterial, and parasitic infections
- DM/PM occurs with collagen vascular disease about 20% of the time
- In DM, humoral immune mechanisms are implicated, resulting in a microangiopathy and muscle ischemia
- In PM, a mechanism of T-cell–mediated cytotoxicity is posited
- CD8 T-cells, along with macrophages, surround and destroy healthy, nonnecrotic muscle fibers that aberrantly express class I major histocompatibility complex (MHC) molecules
- Deposition of complement is the earliest and most specific lesion, followed by inflammation, ischemia, microinfarcts, necrosis, and destruction of the muscle fibers
Pediatric Considerations
- Although DM is seen in both children and adults, PM is rare in children
- Similar to adult DM, juvenile DM (JDM) primarily affects the skin and skeletal muscles
- Juvenile form may include vasculitis, ectopic calcifications (calcinosis cutis), and lipodystrophy
- The juvenile form may be associated with coxsackievirus
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Basics
Description
- Dermatomyositis (DM) and polymyositis (PM) are systemic inflammatory myopathies, which represent the largest group of acquired and potentially treatable causes of skeletal muscle weakness
- Patients experience a marked progression of muscle weakness over weeks to months
- Can lead to respiratory insufficiency from respiratory muscle weakness
- Aspiration pneumonia can occur owing to a weak cough mechanism, pharyngeal muscle dysfunction, and esophageal dysmotility
- Cardiac manifestations include myocarditis, conduction defects, cardiomyopathy, and congestive heart failure (CHF)
- Arthralgias of the hands, wrists, knees, and shoulders with distinct associated skin findings for DM
- Ocular muscles are not involved but facial muscle weakness may be seen in advanced cases
Etiology
- The exact cause is unknown, although autoimmune mechanisms are thought to be largely responsible
- Incidence ∼2:100,000 with a female preponderance
- There may be an association between PM and certain viral, bacterial, and parasitic infections
- DM/PM occurs with collagen vascular disease about 20% of the time
- In DM, humoral immune mechanisms are implicated, resulting in a microangiopathy and muscle ischemia
- In PM, a mechanism of T-cell–mediated cytotoxicity is posited
- CD8 T-cells, along with macrophages, surround and destroy healthy, nonnecrotic muscle fibers that aberrantly express class I major histocompatibility complex (MHC) molecules
- Deposition of complement is the earliest and most specific lesion, followed by inflammation, ischemia, microinfarcts, necrosis, and destruction of the muscle fibers
Pediatric Considerations
- Although DM is seen in both children and adults, PM is rare in children
- Similar to adult DM, juvenile DM (JDM) primarily affects the skin and skeletal muscles
- Juvenile form may include vasculitis, ectopic calcifications (calcinosis cutis), and lipodystrophy
- The juvenile form may be associated with coxsackievirus
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