Texte intégral de l'article
 
  Printable version
  Version PDF

Peeling skin syndrome


European Journal of Dermatology. Volume 16, Number 3, 287-9, May-June 2006, Clinical report


Summary  

Author(s) : Turna İlknur, Melda Demirtaşoğlu, Sevgi Akarsu, Banu Lebe, Ali Tahsin Güneş, Şebnem Özkan , Dept of Dermatology Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey, Department of Pathology, Eylül University, Faculty of Medicine, İzmir, Turkey.

Summary : Peeling skin syndrome is a rare disease characterized by widespread painless peeling of the skin. To date, several cases have been described with different clinical features called peeling skin syndrome. Previous reports describe two types (type A and type B) of peeling skin syndrome, both of which show generalized desquamation, sparing palms and soles. We report a 23-year old man who has been classified as neither type A nor type B, and whose history, clinical features and histopathological findings led to a diagnosis of peeling skin syndrome. In addition, the desquamation pattern in our patient was different from that of both types because our case’s palms and soles were involved too.

Keywords : deciduous skin, keratolysis exfoliativa congenital, peeling skin syndrome

Pictures

Figure 1 Massive shedding from the hands.

Figure 2 Small and delicate scalling from the trunk.

Figure 3 Photomicrograph showing subcorneal epidermal blistering and perivascular mild mononuclear cellular infiltrate in superficial dermis (hematoxylin and eosin; original magnification × 40).