Introduction
Atopic dermatitis (AD) is a chronic relapsing pruritic skin disease in children. Colonization of
Staphylococcus aureus (
S. aureus) is commonly observed in the skin lesions of AD patients,
1) but rare cases can be complicated with deep infections. The breached skin of most AD patients is heavily colonized with
S. aureus. Due to high bacterial density, altered skin barrier, and immune dysregulation, AD can cause normally colonized
S. aureus to penetrate deep into the tissue.
2) Such patients have increased serine protease activity which leads to a compromised skin barrier and possibly increases
S. aureus colonization.
3) Thus, high rate of cutaneous colonization by
S. aureus in AD represents an important source of invasive bacterial infection. Breast abscess is defined a local accumulation of pus within the breast due to infection. Mastitis or breast abscess is an uncommon disease in childhood; however, it occurs in 2 distinct age groups, neonates and adolescents.
4) Breast abscess is a rare but possible complication in childhood AD, and here we report 2 cases with breast abscess in children with AD.
Discussion
We presented 2 cases of breast abscess in adolescent girls with severe AD that was completely cured by proper antibiotics and surgical drainage. Innate immune system abnormalities, including reductions in antimicrobial peptides, diminished recruitment of cells like neutrophils to the skin, and epidermal barrier defects play a role in
S. aureus colonization in the skin of patients with AD.
5,6) Although
S. aureus colonizes affected and unaffected skin in patients with AD, systemic or serious staphylococcal infections are rare. Only a few cases of septic arthritis, bacteremia, or endocarditis have been reported in the literature.
6,7,8,9)
S. aureus is the most commonly found in mastitis or breast abscess.
4) Generally, penicillin or cephalosporin antibiotic is used until drug sensitivity results are retrieved. If the abscess worsens in spite of proper antibiotic use, it may need to be incised and drained. Breast abscess is rare in adolescent girls, primarily occurring in lactating women as well as patients with diabetes mellitus, obesity or immune dysregulation. Tobacco smoking and nipple piercing have been known as risk factors for the development of breast abscess.
10) However, in our 2 patients, there are no preceding conditions inducing breast abscess except for severe AD. There was no evidence of congenital immunodeficiency, such as hypo-gamma-globulinemia or Wiskott-Aldrich syndrome. Rather, extreme dryness and pruritus were more likely to be predisposing factors for staphylococcal colonization and infection in our patients.
Intense scratching in AD is known as a predisposing factor for staphylococcal skin and deep tissue infections. It is believed that our patients' scratching of pruritic skin lesions increased the risk for the penetration and spread of S. aureus into the deep tissue. Not surprisingly, identical strains were found from their breast abscesses, involved and noninvolved skins.
S. aureus is isolated from 2%–25% of healthy skin, and it highly colonizes both the lesional and normal-appearing skin of patients with AD.
11,12) Once attached to the skin,
S. aureus secretes exotoxins with super-antigenic properties that worsen AD.
13) A deficiency in the expression of endogenous antimicrobial peptides in the skin of patients with AD, causing localized immunodeficiency, may account for the susceptibility of these patients to skin invasion with
S. aureus.
11,12) As for humoral immunity, considerable attention has been focused on the importance of the secretory component of immunoglobulin A (sIgA). In a previous study,
6) the amount of sIgA secretion from the skin was significantly lower in AD patients than in healthy subjects and the decrease in sIgA accounted for the high positive skin culture of
S. aureus. Little is known about the onset mechanism of deep tissue infection in AD. However, it is likely that patients with AD habitually scratch the skin due to severe itching, resulting in damage to the skin barrier which causes deep invasion of
S. aureus.
It has been reported that patients with AD have decreased skin microbial diversity and dysbiosis compared to healthy subjects. Patients with AD have increased serine protease activity.
3) Hyperactive serine protease responses appear to be responsible for increased desquamation of the skin, altered cathelicidin, and inflammation.
3,14)
S. aureus serine proteases were directly linked to AD severity, and therefore, this dysbiosis was recovered after treatment.
14,15) Analysis of skin microbiome in our 2 patients also demonstrated low diversity and high
S. aureus loading, suggesting that the microbial landscape of skin may be related to skin immunity and AD.
Treatment of AD with appropriate corticosteroid ointments or emollients reduces the number of colonizing bacteria and the concurrent increase in microbial diversity.
15,16) In our patients, bacterial infections were relatively limited to the breast tissue and no other skin or deep tissue infections were observed. Although we did not demonstrate a deficiency of antimicrobial peptide or a systemic immunodeficiency in our patients, we thought that the skin-localized immunodeficiency or dysbiosis of skin microbiome might contribute to this invasive infection.
AD associated with invasive S. aureus infection is probably underreported. A high rate of cutaneous colonization by S. aureus in AD lesions represents an important source of invasive bacterial infection. Our patients demonstrate the potential severity of bacterial infections in AD. Although breast abscess is rare in AD, it should be recognized as a possible complication in this common skin disorder.
Skin infection by S. aureus commonly occurs in patients with AD. Deep tissue infection is rare but a possible complication in patients with AD, and therefore clinicians should be aware of this complication.