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Actas Dermosifiliogr. 2010 Mar;101(2):168-72.

[Galli-Galli disease presenting as lichenoid papules in the flexures].

[Article in Spanish]

Author information

  • 1Servicio de Dermatología, Hospital Sierrallana, Torrelavega, Cantabria, Spain. igsderma@yahoo.es

Abstract

Galli-Galli disease is a rare genodermatosis currently regarded as an acantholytic variant of Dowling-Degos disease. The 2 diseases have the same clinical features: reticular hyperpigmented macules in the great skin folds, erythematous scaly papules and plaques, comedo-like lesions, and pitted perioral scars, and the only differentiating characteristic is the histological finding of acantholysis, usually without dyskeratosis. We describe the case of a patient with hyperpigmented papules in the skin folds as the only sign of Galli-Galli disease, and we present a review of the literature.

PMID:
20223160
[PubMed - indexed for MEDLINE]
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