Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/484
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dc.contributor.authorSonja Prćićen_US
dc.contributor.authorAleksandra Matićen_US
dc.contributor.authorSlađana Jablanovićen_US
dc.contributor.authorMilan Matićen_US
dc.contributor.authorZorica Gajinoven_US
dc.contributor.authorNataša Stašuken_US
dc.date.accessioned2019-09-23T10:08:02Z-
dc.date.available2019-09-23T10:08:02Z-
dc.date.issued2019-03-01-
dc.identifier.issn428450en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/484-
dc.description.abstract© 2019, Inst. Sci. inf., Univ. Defence in Belgrade. All rights reserved. Introduction. Aplasia cutis congenita (ACC) is a rare condition characterized by the focal absence of skin, and sometimes other underlying structures at birth. It may occur as an isolated defect or associated with other anomalies and defects. Bullous ACC (BACC) is a clinical subtype of the condition with few cases reported in the literature. It presents as a bullous lesion at birth which gradually transforms into an atrophic scar covered by a thin epithelial membrane. It is considered as cutaneous sign of possible neural tube dysraphism. Some cases present with a dark hair around the lesion (the hair collar sign), which can be even more indicative of neural tube defect. However, cases of BACC reported till today are inconclusive regarding this connection. Case report. We report a two cases of BACC of the scalp, in one patient associated with hair collar sign without neural tube defects and the other with hemangioma and we give a brief review of the selected literature. Conclusion. Bullous or membranous aplasia cutis congenita is benign condition, but may represent as a cutaneous marker of occult neural tube defect. Recognising the condition is important in order to rule out associated anomalies.en_US
dc.language.isoenen_US
dc.relation.ispartofVojnosanitetski Pregleden_US
dc.subjectcongenital abnormalitiesen_US
dc.subjectectodermal dysplasiaen_US
dc.subjectscalpen_US
dc.subjecthypertrichosisen_US
dc.subjecthemangiomaen_US
dc.titleBullous aplasia cutis congenita – A report of two cases and brief review of the literatureen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.2298/VSP170201076P-
dc.identifier.scopus2-s2.0-85069437564-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85069437564-
dc.description.versionPublisheden_US
dc.relation.lastpage348en_US
dc.relation.firstpage345en_US
dc.relation.issue3en_US
dc.relation.volume76en_US
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptMedicinski fakultet, Katedra za dermatovenerološke bolesti-
crisitem.author.deptMedicinski fakultet, Katedra za dermatovenerološke bolesti-
crisitem.author.deptMedicinski fakultet, Katedra za dermatovenerološke bolesti-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
Appears in Collections:MDF Publikacije/Publications
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