Differential Diagnosis of ‘Diaper Dermatitis’

   
 
Table 2-2 Differential Diagnosis for Diaper Dermatitis
 Entity Clinical Findings
 
Candidal Dermatitis
Bright red patches with pustules and satellite papules, ± intertriginous involvement (including scrotum), ± thrush
 
Irritant Dermatitis
Poorly demarcated erythematous plaques, spares inguinal folds
 
Seborrheic Dermatitis
Typical salmon-covered scaly patches and plaques involving the scalp, groin, and other intertriginous areas
 
Psoriasis
Sharply demarcated bright pink to red plaques involving inguinal creases, minimal scale; most common psoriatic presentation in infants
 
Allergic Contact Dermatitis
Rare in infants, ± related to topical preparations or foods
 
Atopic Dermatitis
Increased incidence of diaper dermatitis in atopic patients
 
Miliaria
Clear vesicles or erythematous papules/pustules due to blocked
eccrine ducts from heat or humidity in diaper area
 
Granuloma Gluteale Infantum
Red to violaceous granulomatous nodules over the vulva, perianal area, buttocks, ± scrotum; due to irritation, occlusion, candidal infection
 
Perianal Pseudoverrucous Nodules
Erythematous nodules and papules in children with fecal incontinence
 
Acrodermatitis Enteropathica
Erythematous crusted patches/plaques with flaccid bullae in perineal, periorificial, and distal extremities; due to ↓ zinc level (also ↓ alkaline phosphatase as zinc-dependent); may occur in following settings:
 
  1. Premature infants (poor absorption and ↑ requirement of zinc) when weaned off breast milk (which has adequate zinc level)
  2. Inherited form (AR) manifests when weaned off breast milk
  3. Healthy infants if low zinc level in maternal milk
  4. Acquired form if malabsorption or inadequate nutrition
 
Cystic Fibrosis
Resembles acrodermatitis enteropathica, also due to zinc deficiency ± pedal edema, failure to thrive, infections and malabsorption
 
Multiple Carboxylase Deficiency
Both resemble acrodermatitis enteropathica (periorificial dermatitis); treatment for both forms (listed below) is biotin
 
Biotin Deficiency
  1. Neonatal form: AR, holocarboxylase synthetase deficiency, ± erythroderma with alopecia, fatal if not treated
  2. Juvenile form: biotinidase deficiency, ± seizures, alopecia, hearing loss, developmental delay
 
Langerhans Cell Histiocytosis
Yellow-brown crusted papules with purpura in seborrheic distribution; ± systemic involvement; Langerhans cells (CD1a +, S100+)
 
Kawasaki Disease
Tender erythema in perineal area which later desquamates
 
Perianal Strep
Bright red, well-demarcated perianal erythema and involving creases
 
Bullous Impetigo
Honey-colored crusts and flaccid bullae
 
Scabies
Erythematous nodules involving diaper area, ± genitalia
 
Congenital Syphilis
Reddish-brown papulosquamous eruption, may be erosive or bullous