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Review

Neonatal erythroderma – clinical perspectives

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Pages 1-9 | Published online: 22 Jun 2017

Figures & data

Table 1 Causes of infantile erythroderma

Figure 1 Infant with a metabolic disorder, widespread hyperkeratotic scale, but no collodion is present.

Figure 1 Infant with a metabolic disorder, widespread hyperkeratotic scale, but no collodion is present.

Figure 2 Neonate with Netherton syndrome.

Note: Skin is diffusely erythematous with fine scaling.
Figure 2 Neonate with Netherton syndrome.

Figure 3 Psoriasis in infants often localizes to the diaper area.

Note: Periumbilical involvement is also common. Plaques are well demarcated.
Figure 3 Psoriasis in infants often localizes to the diaper area.

Figure 4 A collodion membrane encases this infant’s body, including his feet and toes.

Figure 4 A collodion membrane encases this infant’s body, including his feet and toes.

Figure 5 Algorithm for diagnosis of the erythrodermic infant.

Note: *Ichthyoses include congenital ichthyosiform erythroderma, lamellar ichthyosis, harlequin ichthyosis, and rarely Sjogren–Larsson, trichothiodystrophy, and neutral lipid storage disease.
Figure 5 Algorithm for diagnosis of the erythrodermic infant.

Table 2 Initial diagnostic testing for the erythrodermic infant