Publication:
Lewandowski & Lutz Syndrome: A Rare Case Entity

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorMohan, Rikta
dc.contributor.authorGahalaut, P
dc.contributor.authorSoodan, HS
dc.contributor.authorMishra, N
dc.contributor.authorRastogi, MN
dc.date.accessioned2025-08-21T09:16:40Z
dc.date.available2025-08-21T09:16:40Z
dc.date.issued2017
dc.descriptionRikta Mohan Shri Ram Murti Smarak Institute of Medical Sciences P Gahalaut Shri Ram Murti Smarak Institute of Medical Sciences. HS Soodan Shri Ram Murti Smarak Institute of Medical Sciences. N Mishra Shri Ram Murti Smarak Institute of Medical Sciences. MN Rastogi Shri Ram Murti Smarak Institute of Medical Sciences.
dc.description.abstractAbstract: Epidermodysplasia verruciformis (EV), first described in 1922 by Lewandowski and Lutz, is a rare inherited genetic disease. The disease usually manifests in childhood with highly polymorphic, widespread lesions. We report a case of a fifteen year old boy, who presented to us with multiple flat topped, hypopigmented papules of a seven year duration on his body. He was diagnosed with EV on a skin biopsy, after ruling out differential diagnosis of pityriasis versicolor, verruca vulgaris and acrokeratosisverruciformis. The patient was resistant to known treatment options. Key message: sun protection and lifelong observation for diagnosis and improved prognosis of malignant or premalignant lesions of EV. Keywords: pityriasis versicolor, verruca-like lesions, sun exposed sites
dc.identifierhttps://doi.org/10.3126/njdvl.v15i1.18055
dc.identifier.urihttps://hdl.handle.net/20.500.14572/1902
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.titleLewandowski & Lutz Syndrome: A Rare Case Entity
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage59
oaire.citation.startPage55
relation.isJournalIssueOfPublicationae585fa2-96f9-4b83-8b04-b8efd69bfc01
relation.isJournalIssueOfPublication.latestForDiscoveryae585fa2-96f9-4b83-8b04-b8efd69bfc01
relation.isJournalOfPublicationb2ab7aab-75b0-4bd1-9ed0-b8a91c68201a

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