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A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features

Membranous, bullous, or cystic aplasia cutis congenita is a clinical subtype of aplasia cutis, covered with a membranous or glistening surface. A male newborn presented at birth with two flat lesions on the left parietal scalp, surrounded by a rim of terminal hairs. Physical examination revealed two...

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Autor principal: Lozano-Masdemont, Belén
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514794/
https://www.ncbi.nlm.nih.gov/pubmed/28761263
http://dx.doi.org/10.4103/ijt.ijt_91_16
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author Lozano-Masdemont, Belén
author_facet Lozano-Masdemont, Belén
author_sort Lozano-Masdemont, Belén
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description Membranous, bullous, or cystic aplasia cutis congenita is a clinical subtype of aplasia cutis, covered with a membranous or glistening surface. A male newborn presented at birth with two flat lesions on the left parietal scalp, surrounded by a rim of terminal hairs. Physical examination revealed two translucent papules. On dermoscopy, they showed a reddish background, thin, lineal vessels and, remarkably few hair bulbs could be seen because of the translucency of the lesion. No skull bone and brain defects were found. The diagnosis of membranous aplasia cutis congenita was established. Histologically, it is characterized by an atrophic epidermis with loose fibrovascular stroma and edematous dermal stroma. Dermoscopy may help to rule out other entities (herpes simplex, epidermolysis bullosa, trauma…) since the atrophic epidermis and fibrovascular stroma is evidenced by the hair bulbs and its characteristic translucency (“translucency's sign”).
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spelling pubmed-55147942017-07-31 A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features Lozano-Masdemont, Belén Int J Trichology Case Report Membranous, bullous, or cystic aplasia cutis congenita is a clinical subtype of aplasia cutis, covered with a membranous or glistening surface. A male newborn presented at birth with two flat lesions on the left parietal scalp, surrounded by a rim of terminal hairs. Physical examination revealed two translucent papules. On dermoscopy, they showed a reddish background, thin, lineal vessels and, remarkably few hair bulbs could be seen because of the translucency of the lesion. No skull bone and brain defects were found. The diagnosis of membranous aplasia cutis congenita was established. Histologically, it is characterized by an atrophic epidermis with loose fibrovascular stroma and edematous dermal stroma. Dermoscopy may help to rule out other entities (herpes simplex, epidermolysis bullosa, trauma…) since the atrophic epidermis and fibrovascular stroma is evidenced by the hair bulbs and its characteristic translucency (“translucency's sign”). Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5514794/ /pubmed/28761263 http://dx.doi.org/10.4103/ijt.ijt_91_16 Text en Copyright: © 2017 International Journal of Trichology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Lozano-Masdemont, Belén
A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
title A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
title_full A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
title_fullStr A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
title_full_unstemmed A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
title_short A Case of Membranous Aplasia Cutis Congenita and Dermoscopic Features
title_sort case of membranous aplasia cutis congenita and dermoscopic features
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514794/
https://www.ncbi.nlm.nih.gov/pubmed/28761263
http://dx.doi.org/10.4103/ijt.ijt_91_16
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