Type V aplasia cutis congenita in a preterm newborn successfully resolved
NAGIOS: RODERIC FUNCIONANDO

Type V aplasia cutis congenita in a preterm newborn successfully resolved

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Type V aplasia cutis congenita in a preterm newborn successfully resolved

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dc.contributor.author Silva Díaz, Esmeralda
dc.contributor.author Molini Menchón, Maria Odile
dc.contributor.author Estébanez Corrales, Andrea
dc.contributor.author Garcia Vázquez, Alejandro
dc.contributor.author Estañ Capell, Francisco Javier
dc.contributor.author Sáez Martín, Luis
dc.contributor.author Martín Hernández, Jose
dc.date.accessioned 2020-10-01T07:47:38Z
dc.date.available 2020-10-01T07:47:38Z
dc.date.issued 2020
dc.identifier.uri https://hdl.handle.net/10550/75713
dc.description.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.
dc.language.iso eng
dc.relation.ispartof Dermatologic Therapy, 2020, vol. Jun, num. e13888, p. 1-40
dc.rights.uri info:eu-repo/semantics/openAccess
dc.source Silva Díaz, Esmeralda Molini Menchón, Maria Odile Estébanez Corrales, Andrea Garcia Vázquez, Alejandro Estañ Capell, Francisco Javier Sáez Martín, Luis Martín Hernández, Jose 2020 Type V aplasia cutis congenita in a preterm newborn successfully resolved Dermatologic Therapy Jun e13888 1 40
dc.subject Dermatologia
dc.title Type V aplasia cutis congenita in a preterm newborn successfully resolved
dc.type info:eu-repo/semantics/article
dc.date.updated 2020-10-01T07:47:38Z
dc.identifier.doi https://doi.org/10.1111/dth.13888
dc.identifier.idgrec 140445

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