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Dermatol Ther ; 33(6): e13888, 2020 11.
Article in English | MEDLINE | ID: mdl-32567088

ABSTRACT

Aplasia cutis congenita (ACC) associated with fetus papyraceus is a rare subtype of aplasia cutis categorized as type V in Frieden's classification. It is characterized by stellate lesions in a symmetrical distribution over the trunk and proximal extremities. Conservative treatment is recommended, but there is not a well-defined therapeutic protocol. We report the case of a type V ACC in a preterm male newborn with lesions on the trunk and scalp successfully treated with topical 1% silver sulfadiazine and petrolatum gauze with an excellent evolution. This case associates a severe affectation of the scalp which represents a rare variant of type V ACC.


Subject(s)
Ectodermal Dysplasia , Bandages , Ectodermal Dysplasia/diagnosis , Ectodermal Dysplasia/therapy , Humans , Infant, Newborn , Male , Petrolatum , Scalp , Torso
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