Peeling skin syndrome in Infant/Neonate
PSS often presents in infancy but can present in late childhood and occasionally adulthood. Skin loss in PSS is generally asymptomatic but is occasionally pruritic. Peeling is worsened by trauma, friction, humidity, heat, and water exposure.
PSS is divided into generalized and acral subtypes. Generalized PSS causes diffuse skin shedding that typically spares mucosal surfaces, palms, and soles. It may be noninflammatory (type A) or inflammatory (type B).
- Noninflammatory PSS is asymptomatic and has been associated with hyperpigmentation. The CHST8 gene on chromosome 19 is a candidate gene. Inflammatory PSS can present with erythema, pruritus, and occasional flaccid vesicles.
- Inflammatory PSS can worsen during summer months. An association with atopy and high IgE levels may be seen. Loss of function mutations in the CDSN gene on chromosome 6 is responsible.
- Acral PSS (APSS) is a localized disease involving the dorsal and volar surfaces of the hands and feet. Mutations in the transglutaminase 5 (TGM5) gene on chromosome 15 are found.
R23.4 – Changes in skin texture
238643009 – Skin peeling disorder
Other causes of peeling skin include:
- Netherton syndrome – differentiate from the inflammatory generalized subtype. Ichthyosis linearis circumflexa, trichorrhexis invaginata, and immunological dysfunction accompany Netherton syndrome.
- Epidermolysis bullosa simplex (EBS) – differentiate from the acral subtype. EBS has larger, more persistent bullae than APSS.
- Staphylococcal scalded skin syndrome
- Superficial epidermolytic ichthyosis
- Pemphigus vulgaris – can involve mucous membranes, unlike PSS
- Severe dermatitis, multiple allergies, and metabolic wasting (SAM) syndrome
- Atopic dermatitis