Publication:
A Rare Case of Idiopathic Atrophoderma of Pasini and Pierini

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorXiao, Hui
dc.contributor.authorPradhan, Sushmita
dc.contributor.authorYang, Xingchun
dc.contributor.authorLiu, Jiaxiu
dc.contributor.authorZhu, Tangyou
dc.date.accessioned2025-10-06T11:23:34Z
dc.date.available2025-10-06T11:23:34Z
dc.date.issued2023
dc.descriptionAuthor Biographies Hui Xiao, Chengdu BOE Hospital, Chengdu, China Consultant Dermatologist, Department of Dermatovenereology, Chengdu BOE Hospital, Chengdu, China Sushmita Pradhan, Province Hospital, Karnali Province, Birendranagar, Surkhet, Nepal Consultant Dermatologist, Department of Dermatology and Venereology, Province Hospital, Karnali Province, Birendranagar, Surkhet, Nepal Xingchun Yang, Chengdu BOE Hospital, Chengdu, China Consultant Dermatologist, Department of Dermatovenereology, Chengdu BOE Hospital, Chengdu, China Jiaxiu Liu, Chengdu BOE Hospital, Chengdu, China Consultant Dermatologist, Department of Dermatovenereology, Chengdu BOE Hospital, Chengdu, China Tangyou Zhu, Chengdu BOE Hospital, Chengdu, China Professor, Department of Dermatovenereology, Chengdu BOE Hospital, Chengdu, China
dc.description.abstractAbstract: Idiopathic atrophoderma of Pasini and Pierini (IAPP) is a rare pigmented atrophic cutaneous disease. Here, we report a case of a 27-year-old woman who presented with asymptomatic brown patches on her upper back for one year. There was no prior history of swelling or induration of the lesions. Physical examination showed atrophic patches with clear boundaries, consistent with snow footprints or cliff-drop-like changes on edge. Dermoscopy revealed numerous bare linear, branched blood vessels and perifollicular brownish areas, which differs from only one previously reported IAPP. Biopsy showed perivascular mononuclear cells infiltrating the dermis and reduced elastic fibers in the upper and middle dermis. Typical clinical findings of “footprints in the snow” appearance and dermoscopy could combine for a definite diagnosis aiding in differentiating from morphea presenting with whitish structureless and hairless areas. This case report might stimulate clinicians to diagnose such a rare disease in patients with similar lesions to avoid unnecessary treatment.
dc.identifierhttps://doi.org/10.3126/njdvl.v21i1.48558
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2447
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.subjectAtrophoderma of Pasini and Pierini
dc.subjectDermoscopy
dc.subjectIdiopathic
dc.subjectRare disease
dc.titleA Rare Case of Idiopathic Atrophoderma of Pasini and Pierini
dc.typeArticle
dspace.entity.typePublication
local.article.typeLetters to the Editor
oaire.citation.endPage57
oaire.citation.startPage55
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