Widespread presentation and spontaneous regression of porokeratotic eccrine ostial and dermal duct nevus
dc.contributor.author | Petkiewicz, Stephanie | |
dc.contributor.author | Baltz, Julia | |
dc.contributor.author | Cornejo, Kristine M. | |
dc.contributor.author | Deng, April C. | |
dc.contributor.author | Wiss, Karen | |
dc.date | 2022-08-11T08:09:51.000 | |
dc.date.accessioned | 2022-08-23T16:46:13Z | |
dc.date.available | 2022-08-23T16:46:13Z | |
dc.date.issued | 2018-10-29 | |
dc.date.submitted | 2018-12-07 | |
dc.identifier.citation | <p>JAAD Case Rep. 2018 Oct 29;4(10):972-975. doi: 10.1016/j.jdcr.2018.08.001. eCollection 2018 Nov. <a href="https://doi.org/10.1016/j.jdcr.2018.08.001">Link to article on publisher's site</a></p> | |
dc.identifier.issn | 2352-5126 (Linking) | |
dc.identifier.doi | 10.1016/j.jdcr.2018.08.001 | |
dc.identifier.pmid | 30406170 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/40836 | |
dc.description.abstract | Porokeratotic eccrine ostial and dermal duct nevus (PEODDN) is an uncommon hamartomatous growth with disordered keratinization. The lesions typically appear on the limbs, often at birth or in early childhood, as linearly distributed papules and plaques. We report 4 cases of PEODDN, 2 of which showed significant spontaneous regression. | |
dc.language.iso | en_US | |
dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30406170&dopt=Abstract">Link to Article in PubMed</a></p> | |
dc.rights | Copyright 2018 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | PEODDN | |
dc.subject | Porokeratotic eccrine ostial and dermal duct nevus | |
dc.subject | porokeratosis | |
dc.subject | resolution | |
dc.subject | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | |
dc.subject | Dermatology | |
dc.subject | Pathological Conditions, Signs and Symptoms | |
dc.subject | Skin and Connective Tissue Diseases | |
dc.title | Widespread presentation and spontaneous regression of porokeratotic eccrine ostial and dermal duct nevus | |
dc.type | Journal Article | |
dc.source.journaltitle | JAAD case reports | |
dc.source.volume | 4 | |
dc.source.issue | 10 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4654&context=oapubs&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/3642 | |
dc.identifier.contextkey | 13442263 | |
refterms.dateFOA | 2022-08-23T16:46:13Z | |
html.description.abstract | <p>Porokeratotic eccrine ostial and dermal duct nevus (PEODDN) is an uncommon hamartomatous growth with disordered keratinization. The lesions typically appear on the limbs, often at birth or in early childhood, as linearly distributed papules and plaques. We report 4 cases of PEODDN, 2 of which showed significant spontaneous regression.</p> | |
dc.identifier.submissionpath | oapubs/3642 | |
dc.contributor.department | Department of Pathology | |
dc.contributor.department | Department of Dermatology | |
dc.source.pages | 972-975 |