Impetigo and Ecthyma
Impetigo, a highly contagious, common primary skin infection in children, is most frequently found on the face, scalp, or extremities. It begins as scattered, discrete macules that itch and are spread by scratching. These macules then develop into vesicles and pustules on an erythematous base that eventually rupture, oozing a purulent liquid. Once dried, the lesions appear thick, with a characteristic honey-colored crust on the surface. Once healed, scarring is rare. Regional lymphadenopathy may be present, and lesions may itch; however, fever or other systemic complaints are uncommon. The infection is diagnosed clinically by the appearance of hallmark honey-colored crusts. A Gram stain of the vesicular fluid can confirm the diagnosis if there is clinical uncertainty.
Impetigo may also present with bullous lesions and can be referred to as bullous impetigo. Found on the face, scalp, extremities, trunk, and intertriginous areas, it affects primarily newborns and children ages 3 to 5 (
Wilhelm & Edson, 2001). Bullous impetigo is characterized by the formation of superficial, flaccid bullae on the skin. The brownish-gray lesions are sometimes crusted or have an erythematous halo. They also appear to be smooth and shiny, as if they were coated with lacquer.
In the most severe form of bullous impetigo, exfoliation of large areas of the skin can occur in what is called “scalded skin” syndrome. This presentation is most common in infants but can also occur in those who are immunosuppressed. It is thought to occur more often in patients who are sensitive to toxins produced by staphylococcal organisms (
Barg et al., 1998). Such cases carry a greater risk for more invasive infection because of the loss of large amounts of the skin, the body’s protective barrier.
Ecthyma occurs when a case of impetigo worsens and spreads deeply to the dermis. Much less common than impetigo, ecthyma usually affects debilitated individuals and the elderly (
Odell, 2003). Signs of ecthyma are usually found on the lower extremities, beginning with the formation of vesicles that then develop into shallow ulcerations. The ulcerations enlarge over several days and are surrounded by an erythematous halo. Because the infection affects the deeper layers of the skin, scarring is often seen after ulcerations heal (
Wilhelm & Edson, 2001). Lesions are usually painful and may persist for weeks to months.
Cellulitis and Erysipelas
Cellulitis is a potentially serious infection involving the skin and subcutaneous tissue. In adults, it most commonly affects the lower extremities and begins with a skin break resulting from a localized trauma that may not be apparent. In children, cellulitis usually results from an insect bite or wound. The disease can spread through the superficial layers of skin and cause painful erythema, with the affected area warm and tender to the touch. Pitting edema can also be present, and the skin may be shiny and have an “orange peel” appearance. The margins of cellulitis are diffuse, not sharply demarcated, and the affected area is flat and usually edematous. In open wounds, purulent drainage and necrosis may be present. Red streaks may develop proximal to the area of infection, indicating lymphatic spread or lymphangitis. Crepitus may be present, suggesting involvement of anaerobic organisms. Systemic symptoms of fever, chills, and malaise and regional adenitis are also common and can indicate bacteremia. In fact, these symptoms may be present before cellulitis is clearly evident.
Cellulitis due to CA-MRSA may be accompanied by the presence of an abscess or a furuncle that contains a necrotic center (
DeLeo et al., 2010). These infections may progress rapidly and cause local tissue destruction, possibly leading to systemic infection. In addition to painful erythema, the abscess present may spontaneously drain but often will require an incision and drainage procedure for proper management.
Erysipelas, a type of cellulitis limited to the superficial layers of the skin, is most common in children, especially infants and the elderly, but it can occur in healthy individuals who have sustained only minor wounds. Other patients who are at risk include those with venous insufficiency or underlying skin ulcers, diabetics, alcoholics, or those with nephritic syndrome. Erysipelas is most commonly found on the lower extremities but can also be present on the face and scalp. Erysipelas begins as an area of sharply demarcated erythema that spreads rapidly over a period of minutes to hours. The affected area is slightly raised, firm, warm, and tender to the touch. Erythema spreads along local lymphatic channels, which gives the skin a typical “orange peel” appearance due to lymphatic obstruction.
Common systemic symptoms include pain, malaise, chills, and fever. In more serious cases, patients may appear seriously ill. Erysipelas occurring on the face often follows a respiratory infection; this presentation can be particularly serious due to the potential occurrence of cavernous sinus thrombosis (
Odell, 2003). Erysipelas can recur, usually in the same area as a previous infection, especially in patients with venous insufficiency or lymphedema (
Wilhelm & Edson, 2001).