Publication:
Angiolymphoid Hyperplasia with Eosinophilia- Think Twice with Scalp Papules! A Case Report

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorAgarwal, Pooja
dc.contributor.authorBaxi, Kalgi
dc.contributor.authorShah, Malhar
dc.date.accessioned2025-10-08T07:55:46Z
dc.date.available2025-10-08T07:55:46Z
dc.date.issued2023
dc.descriptionPooja Agarwal Smt N.H.L. Medical College, Ahmedabad, Gujarat, India https://orcid.org/0000-0001-8316-3259 Kalgi Baxi Smt N.H.L. Medical College, Ahmedabad, Gujarat, India Malhar Shah Geetanjali Medical College and Hospital, Udaipur, Rajasthan, India
dc.description.abstractAbstract: Angiolymphoid hyperplasia is an uncommon condition characterized by multiple erythematous papules and nodules which are vascular and present over the head and neck area, predominantly around the ears. It is a benign condition but treatment is often sought for the appearance of lesions. We report a case that had a recurrence of erythematous lesions after incomplete electrocoagulation and the diagnosis of angiolymphoid hyperplasia with eosinophilia was confirmed on histopathological evaluation after complete excision of the lesion. In conclusion, as angiolymphoid hyperplasia can be clinically misdiagnosed, histopathological evaluation is warranted in erythematous nodules presenting over the sites of predilection.
dc.identifierhttps://doi.org/10.3126/njdvl.v21i2.56601
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2495
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.subjectAngiolymphoid Hyperplasia
dc.subjectEosinophilia
dc.subjectScalp
dc.titleAngiolymphoid Hyperplasia with Eosinophilia- Think Twice with Scalp Papules! A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage40
oaire.citation.startPage39
relation.isJournalIssueOfPublication3540225c-097a-4d28-8638-10fe9f159169
relation.isJournalIssueOfPublication.latestForDiscovery3540225c-097a-4d28-8638-10fe9f159169
relation.isJournalOfPublicationb2ab7aab-75b0-4bd1-9ed0-b8a91c68201a

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