The occurrence of two cases of bullous congenital ichtyosiform erythroderma (BCIE) in a mother and son is reported. Clinical diagnosis was confirmed by histological and ultrastructural findings, which demonstrated marked changes in the cytoskeleton of the keratinocytes of the Malpighian layer and areas of cytolysis and hypoplasia of the tonofilament-hemidesmosome complexes in the cells of the granulous layer. These results and the possible aetiopathogenic mechanisms are discussed in the light of the most recent data in the literature. Treatment with oral etretinate proved to be helpful, but not long lasting.

Simoni, S., Romano, C., Bilenchi, R., Alessandrini, C., Fimiani, M. (1989). Bullous congenital ichthyosiform erythroderma in a mother and son. GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA, 124(3), 97-102.

Bullous congenital ichthyosiform erythroderma in a mother and son

ROMANO, C.;BILENCHI, R.;FIMIANI, M.
1989-01-01

Abstract

The occurrence of two cases of bullous congenital ichtyosiform erythroderma (BCIE) in a mother and son is reported. Clinical diagnosis was confirmed by histological and ultrastructural findings, which demonstrated marked changes in the cytoskeleton of the keratinocytes of the Malpighian layer and areas of cytolysis and hypoplasia of the tonofilament-hemidesmosome complexes in the cells of the granulous layer. These results and the possible aetiopathogenic mechanisms are discussed in the light of the most recent data in the literature. Treatment with oral etretinate proved to be helpful, but not long lasting.
1989
Simoni, S., Romano, C., Bilenchi, R., Alessandrini, C., Fimiani, M. (1989). Bullous congenital ichthyosiform erythroderma in a mother and son. GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA, 124(3), 97-102.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/2678
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