Type V aplasia cutis congenita in a preterm newborn successfully resolved

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 recommend...

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Veröffentlicht in:Dermatologic therapy 2020-11, Vol.33 (6), p.e13888-n/a
Hauptverfasser: Silva Díaz, Esmeralda, Molini Menchón, Maria Odile, Estébanez Corrales, Andrea, Garcia‐Vázquez, Alejandro, Estañ Capell, Javier, Sáez‐Martín, Luis, Martín Hernández, Jose
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container_issue 6
container_start_page e13888
container_title Dermatologic therapy
container_volume 33
creator Silva Díaz, Esmeralda
Molini Menchón, Maria Odile
Estébanez Corrales, Andrea
Garcia‐Vázquez, Alejandro
Estañ Capell, Javier
Sáez‐Martín, Luis
Martín Hernández, Jose
description 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.
doi_str_mv 10.1111/dth.13888
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source MEDLINE; Wiley Journals
subjects aplasia cutis congenita
Bandages
Ectodermal Dysplasia - diagnosis
Ectodermal Dysplasia - therapy
Humans
Infant, Newborn
Male
Petrolatum
Scalp
Torso
treatment ACC
type V ACC
title Type V aplasia cutis congenita in a preterm newborn successfully resolved
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