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Skin and soft tissue infections (SSTIs) are common in children. They usually are recognized easily and treated with few residual long-term problems. However, myositis, pyomyositis, and necrotizing fasciitis are soft tissue infections that can be difficult to diagnose in their early stages, and despite appropriate antibiotic therapy, they can be associated with substantial morbidity and mortality.
The epidemiology of SSTIs is evolving, and the incidence among children is increasing. Community-associated, methicillin-resistant S. aureus (CA-MRSA) first emerged among children in the 1990s. Since then, CA-MRSA has become the predominant cause of purulent SSTIs in the United States. Coincident with this epidemic, the incidence of pediatric ambulatory visits for SSTIs has almost tripled. SSTIs can be atypical and more severe in immunocompromised children.
Myositis is inflammation of a muscle, typically a voluntary muscle, characterized by pain, tenderness, swelling, and weakness. Causes of myositis include infection, autoimmune conditions, genetic disorders, medications, electrolyte disturbances, and diseases of the endocrine system. Infectious myositis can be caused by bacteria, fungi, parasites, and viruses ( Table 74.1 ).
Organism Group | Organisms |
---|---|
Gram-positive bacteria | Staphylococcus aureus |
Streptococcus pyogenes (group A Streptococcus ) | |
Streptococcus (groups B, C, and G; S. pneumoniae; S. anginosus ) | |
Gram-negative bacteria | Aeromonas hydrophila |
Citrobacter freundii | |
Enterobacter spp. | |
Escherichia coli | |
Proteus spp. | |
Pseudomonas spp. | |
Salmonella spp. | |
Vibrio vulnificus | |
Anaerobic bacteria | Bacteroides spp. |
Clostridium spp. | |
Streptococcus spp. (anaerobic, e.g., Peptostreptococcus ) | |
Mycobacterium spp. | Mycobacterium tuberculosis |
Fungi | Candida spp. |
Parasites | Trachipleistophora |
Plasmodium spp. | |
Sarcocystis spp. | |
Taenia solium | |
Trichinella spp. | |
Viruses | Enteroviruses (coxsackievirus B and echovirus) |
Human immunodeficiency virus (HIV) | |
Human T-lymphotropic virus type 1(HTLV-1) | |
Influenza A and B viruses |
The clinical course can be acute, subacute, or chronic. Although identification of the causative microbe requires specific diagnostic testing (e.g., cultures), some clinical findings suggest the general category of the agent. For example, bacterial myositis usually causes focal muscle infection, whereas viruses and parasites often cause generalized myalgias or multifocal myositis. Bacterial myositis often occurs in the setting of muscular injury, surgery, ischemia, or a foreign body.
Acute bacterial myositis, defined as a diffuse muscle infection without an intramuscular abscess, occurs less commonly than pyomyositis and psoas abscess formation. Compared with pyomyositis, myositis is more often seen in adults than children.
Although S. aureus myositis is uncommon, the incidence has increased among adults and children in recent years, largely due to the emergence of CA-MRSA. , In the US, the USA300 clone of CA-MRSA accounts for most infections, although USA300 clones of methicillin-susceptible S. aureus are similarly challenging. It appears that virulence has evolved in the USA300 clonal type through the increased expression of core genome-encoded virulence determinants, such as the two-component exotoxins (e.g., LukAB, LukDE, α-hemolysin, phenol-soluble modulins) and acquisition of the phage-encoded Panton-Valentine leukocidin (PVL) genes. Each of these toxins impact disease progression in animal models of USA300 infection. The basis of virulence in other CA-MRSA epidemics is less well understood.
S. pyogenes (i.e., group A Streptococcus [GAS]) can cause myositis. The most severe form is necrotizing myositis (i.e., streptococcal myonecrosis or spontaneous streptococcal gangrenous myositis).
Cases typically occur among adult men and young adults. The disease usually occurs spontaneously without a history of penetrating trauma or underlying immunosuppression. The portal of entry often is unknown. Some cases begin with a sore throat, suggesting that pharyngitis might have led to bacteremia and seeding of the muscle, but most cases occur without an antecedent illness.
The clinical presentation includes an initial prodromal stage with flu-like symptoms, which may include rash and myalgia. This progresses to intense local muscle pain that is disproportionate to clinical findings and to local tense swelling and fever. The course can evolve rapidly over several hours ( Fig. 74.1 ).
Clostridial gas gangrene (i.e., myonecrosis) most commonly is caused by Clostridium perfringens, C. novyi, C. histolyticum, and C. septicum . C. perfringens is the most frequent cause of trauma-associated gas gangrene. Infection occurs in a variety of settings: traumatic wounds with soil contamination, surgery involving the bowel or biliary system, septic abortions, vascular disease with arterial insufficiency, and injection of medications (e.g., epinephrine) or illicit drugs (e.g., heroin). Common inciting events include contamination of the site with Clostridium spp. (which exist in the soil and as part of the gastrointestinal [GI] flora of humans) and devitalized tissue. A foreign body is also a risk factor. In contrast to traumatic gas gangrene, spontaneous gangrene is principally associated with the more aerotolerant C. septicum and occurs predominantly in patients with underlying GI conditions, including occult colon cancer, bowel infarction, or neutropenic enterocolitis.
C. septicum infections occur in children with three major predispositions: neutrophil dysfunction (e.g., malignancies, congenital or cyclic neutropenia, aplastic anemia), bowel ischemia (e.g., hemolytic uremic syndrome, intussusception), and trauma. Malignancy underlies more than 50% of cases; acute myelocytic and lymphocytic leukemias are the most common. Cyclic and congenital neutropenia is identified in 20% of the published pediatric cases.
Clinical features associated with C. septicum infections in children include fever, vomiting, diarrhea, hematochezia, anorexia, and acute abdomen or distention . Despite treatment with surgery and parenteral antibiotics, mortality rates for children with C. septicum infections remain higher than 50%.
Presenting symptoms of clostridial myonecrosis include intense pain, edema, and a sweet-smelling discharge that occur several hours to a few days after injury. The wound is initially pale but can evolve to a bronze color with hemorrhagic bullae. Classic findings include gas in the tissues detected by gas bubbles emitted from the wound or seen on radiographic films. Although gas often is considered to be essential for a diagnosis of gas gangrene, the absence of crepitus or gas on examination should not deter consideration of this diagnosis. Failure of the muscle to contract on stimulation and lack of bleeding of the wound during operation are characteristic findings.
Typical laboratory findings include leukocytosis and a hemolytic anemia due to clostridial α-toxin. Bacteremia occurs in 15% of cases. Gram stain evaluation of the wound exudate usually shows a lack of neutrophils and an abundance of gram-positive bacilli with blunt ends.
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