Erythrodermy neonatalL53.9

Clinical special cases of disease patterns that may be associated with erythroderma in newborns and young infants. S.u. Erythrodermia in newborns and infants.

Differential diagnosis of erythroderma in newborns and young infants.

• Infections:
• Staphylococcal Scalded Skin Syndrome
• Candidosis, congenital cutaneous
• shock syndrome, toxic
• Neonatal toxic-shock-like exanthematous disease.
• Immunodeficiency syndromes:
• Primary T-cellular immunodeficiencies (e.g. Omenn syndrome)
• Graft-versus-host disease, acute.
• Ichthyosis:
• Non-bullous ichtyosiform erythroderma (Erythrodermia congenitalis ichthyosiformis nonbullosa)
• Bullous congenital erythroderma ( Erythrodermia congenitalis ichthyosiformis bullosa)
• Netherton Syndrome
• Chondrodysplasia punctata (Conradi-Hünermann syndrome).
• Metabolic diseases:
• Deficiency of essential fatty acids
• multiple carboxylase deficiency
• Fibrosis, cystic (mucoviscidosis).
• Drug-induced:
• Ceftriaxone
• Vancomycin.
• Other:
• Eczema, atopic
• Eczema, seborrhoic
• psoriasis vulgaris
• pityriasis rubra pilaris
• Mastocytosis, diffuse.