Publication:
Pseudoxanthoma Elasticum a Rare Genetic Disorder : A Case Report

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorPandit, Shashwata Raj
dc.contributor.authorKhadka, Anupa
dc.contributor.authorJha, Ayush
dc.contributor.authorShrestha, Rima
dc.contributor.authorShrestha, Ravina Bade
dc.date.accessioned2025-10-08T10:34:16Z
dc.date.available2025-10-08T10:34:16Z
dc.date.issued2024
dc.descriptionShashwata Raj Pandit Kist Medical College and Teaching Hospital, Nepal https://orcid.org/0009-0007-9769-0106 Anupa Khadka Kist Medical College and Teaching Hospital, Nepal Ayush Jha Kist Medical College and Teaching Hospital, Nepal Rima Shrestha Kist Medical College and Teaching Hospital, Nepal Ravina Bade Shrestha Kist Medical College and Teaching Hospital, Nepal
dc.description.abstractAbstract: Pseudoxanthoma elasticum (PXE) is a rare hereditary condition marked by the accumulation of fragmented and calcified elastic fibers in the body's tissues, leading to skin, vascular, and ocular involvement. In clinical practice, the most prevalent and typically earliest indication of PXE is observed through skin manifestations, which include laxity and the presence of yellowish papules and plaques. Here we report a case of a 40-year-old woman from Nepal presenting with yellowish multiple papules and plaque around the neck and axilla for 20 years, slowly increasing in size and number. A skin biopsy revealed fragmented eosinophilic elastic fibers in the dermis, consistent with PXE. Echocardiography, slit lamp, and indirect ophthalmoscopic examination were done.
dc.identifierhttps://doi.org/10.3126/njdvl.v22i1.63063
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2513
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.subjectAngioid Streaks
dc.subjectElastic Fibers
dc.subjectPseudoxanthoma Elasticum
dc.titlePseudoxanthoma Elasticum a Rare Genetic Disorder : A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage67
oaire.citation.startPage65
relation.isJournalIssueOfPublication30bad17b-0be4-4009-a6cf-dffc34b4fe05
relation.isJournalIssueOfPublication.latestForDiscovery30bad17b-0be4-4009-a6cf-dffc34b4fe05
relation.isJournalOfPublicationb2ab7aab-75b0-4bd1-9ed0-b8a91c68201a

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