Gougerot-Carteaud syndrome or confluent and reticulated papillomatosis (CRP), was first described by Gougerot and Carteaud as dermatosis. It is generally considered a rare condition. The eruption consists confluent, flat, brown papules localized primarily to the intermammary and interscapular regions with subsequent spread to the breast and abdomen; at the periphery, the papules spread out forming a pigmented reticulated pattern. At present, the aetiology of CRP remains unknown. The two prominent theories are an abnormal host response to fungi and a keratinization defect. Other hypothesis include photosensitivity, genetic factor, amylodosis cutis and endocrinopathy.

Maria Carrozzo, A., Gatti, A., Ferranti, G., Primavera, G., Paro Vidolin, A., Nini, G. (2000). Calcipotriol treatment of confluent and reticulated papillomatosis (Gougerot-Carteaud syndrome), 14(2), 131-133 [10.1046/j.1468-3083.2000.00032.x].

Calcipotriol treatment of confluent and reticulated papillomatosis (Gougerot-Carteaud syndrome)

GATTI, ANTONIO;
2000-01-01

Abstract

Gougerot-Carteaud syndrome or confluent and reticulated papillomatosis (CRP), was first described by Gougerot and Carteaud as dermatosis. It is generally considered a rare condition. The eruption consists confluent, flat, brown papules localized primarily to the intermammary and interscapular regions with subsequent spread to the breast and abdomen; at the periphery, the papules spread out forming a pigmented reticulated pattern. At present, the aetiology of CRP remains unknown. The two prominent theories are an abnormal host response to fungi and a keratinization defect. Other hypothesis include photosensitivity, genetic factor, amylodosis cutis and endocrinopathy.
2000
Pubblicato
Rilevanza internazionale
Altro
Sì, ma tipo non specificato
Settore MED/41 - ANESTESIOLOGIA
English
Calcipotriol; Gougerot-Carteaud syndrome
Maria Carrozzo, A., Gatti, A., Ferranti, G., Primavera, G., Paro Vidolin, A., Nini, G. (2000). Calcipotriol treatment of confluent and reticulated papillomatosis (Gougerot-Carteaud syndrome), 14(2), 131-133 [10.1046/j.1468-3083.2000.00032.x].
Maria Carrozzo, A; Gatti, A; Ferranti, G; Primavera, G; Paro Vidolin, A; Nini, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/49805
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