| Basics | Clinical Manifestations | Diagnosis and Treatment |
Infections | | | |
Candidal diaper dermatitis (Fig. 2.18) | Candidal infection of skin, common May be triggered by recent systemic antibiotic use, diarrhea, and oral thrush. In chronic, recurrent cases candida may be present in patient's GI tract | Bright beefy red, well-demarcated scaly patches, collarette of scale at edge, and characteristic satellite papulopustules Unlike irritant diaper dermatitis, the inguinal fold is usually affected Can also be seen in oral mucosa and other intertriginous areas | A KOH will be positive and show pseudohyphae and budding yeast Topical anti-candida treatments including miconazole 2% cream, nystatin cream, or ketoconazole 2% cream. In resistant cases oral therapy with nystatin or fluconazole is required |
Bullous impetigo (Fig. 2.19) | Infection with a toxin producing strain of Staphylococcus aureus that separates the upper layers of the epidermis Moisture and warmth can promote bacterial growth; sometimes umbilicus is colonized with the S. aureus | Early: small vesicles that enlarge to 1-2-cm superficial bullae Late: larger flaccid bullae, rupture easily leaving a collarette of scale, no thick crust, and usually no surrounding erythema Favors diaper area in newborns but also seen periumbilical, face, trunk, and body folds | Gram stain: gram-positive cocci in clusters; bacterial culture + S. aureus Treat with topical antibiotics (mupirocin 2% ointment or fusidic acid cream or ointment); oral antibiotics are used if there are systemic findings or not improving with topicals (cephalexin) |
Inflammatory conditions | | | |
Seborrheic dermatitis | Results from increased activity of sebaceous glands secondary to elevated hormone levels in early infancy | Salmon-colored scaly plaques with greasy yellow scale Usually involves the inguinal folds and convex surfaces. Occasionally fissuring is seen No satellite lesions Typically eruption will also be present in other body folds, face, and/or scalp | Diagnosis is based on clinical recognition Responds quickly to low-potency topical corticosteroid (hydrocortisone 2.5% ointment) and/or topical antifungals (ketoconazole 2% cream). Spontaneous clearance |
Psoriasis (Fig. 2.20) | Psoriasis is overall rare in infancy; however, diaper dermatitis with dissemination is the most common presentation of psoriasis in children <2 yrs. A positive family history of psoriasis may be present | Sharply demarcated confluent erythematous plaques, involve inguinal folds, typical scale of psoriasis may be lacking due to moisture in the diaper area Typical psoriasis lesions may be present elsewhere | Psoriasis will take longer to clear than seborrheic dermatitis and will require a more potent topical corticosteroid (hydrocortisone valerate 0.2% or desonide 0.05% ointment) |
Atopic dermatitis (Fig. 2.21) | Uncommonly seen in the diaper area, typically in the inguinal creases | Appears similar to irritant dermatitis (shiny, wrinkled eczematous plaques) but is more chronic and resistant to treatment Is intensely itchy. Usually typical eczematous plaques are present elsewhere on body | Topical corticosteroids, frequent diaper changes, application of thick barrier ointment with each diaper change. Avoidance of harsh soaps and overuse of wipes |
Jacquet dermatitis (Fig. 2.22) | Represents the severe end of the spectrum of irritant diaper dermatitis | A severe erosive eruption, well-demarcated papules, nodules, and punched-out ulcerations, typically on the perianal skin | Management is similar to irritant dermatitis, frequent changes, application of thick barrier ointment with each diaper change, low threshold for antimicrobial treatment if not improving |
Other | | | |
Langerhans cell histiocytosis (Fig. 2.23) | Rare disease characterized by infiltration of Langerhans cells into various organs of the body | In infants, typically presents as a seborrheic dermatitis-like eruption admixed with petechial and purpuric papules some with red-brown crusting. Fails to respond to treatment Lesions can also be seen on the scalp and trunk Can involve skin only or skin + other organ systems | A skin biopsy can confirm the diagnosis in suspected cases Treatment depends on extent of extracutaneous involvement |
Acrodermatitis enteropathica (Fig. 2.24A,B) | Rare condition caused by zinc deficiency that usually results from an inherited inability to absorb zinc; less often is acquired due to low levels of zinc in diet (or in maternal milk) or malabsorption from intestinal disease | Well-demarcated scaly plaques in the perineal skin and inguinal folds. Occasionally erosions, vesicles, and bullae. Older lesions become thick with drier scale. Typically, lesions are also present around the mouth and on hands and feet. Usually there is associated diarrhea and alopecia | Diagnosis is confirmed by detection of plasma zinc levels of <50 ug/mL and a low alkaline phosphatase Responds quickly to zinc supplementation |