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dc.contributor.authorPetkiewicz, Stephanie
dc.contributor.authorBaltz, Julia
dc.contributor.authorCornejo, Kristine M.
dc.contributor.authorDeng, April
dc.contributor.authorWiss, Karen
dc.date2022-08-11T08:09:51.000
dc.date.accessioned2022-08-23T16:46:13Z
dc.date.available2022-08-23T16:46:13Z
dc.date.issued2018-10-29
dc.date.submitted2018-12-07
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.issn2352-5126 (Linking)
dc.identifier.doi10.1016/j.jdcr.2018.08.001
dc.identifier.pmid30406170
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40836
dc.description.abstractPorokeratotic 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.isoen_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.rightsCopyright 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.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectPEODDN
dc.subjectPorokeratotic eccrine ostial and dermal duct nevus
dc.subjectporokeratosis
dc.subjectresolution
dc.subjectCongenital, Hereditary, and Neonatal Diseases and Abnormalities
dc.subjectDermatology
dc.subjectPathological Conditions, Signs and Symptoms
dc.subjectSkin and Connective Tissue Diseases
dc.titleWidespread presentation and spontaneous regression of porokeratotic eccrine ostial and dermal duct nevus
dc.typeJournal Article
dc.source.journaltitleJAAD case reports
dc.source.volume4
dc.source.issue10
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4654&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3642
dc.identifier.contextkey13442263
refterms.dateFOA2022-08-23T16:46:13Z
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.submissionpathoapubs/3642
dc.contributor.departmentDepartment of Pathology
dc.contributor.departmentDepartment of Dermatology
dc.source.pages972-975


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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/).
Except where otherwise noted, this item's license is described as 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/).