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Pseudobullous pilomatricoma: A rare variant of pilomatricoma
Pilomatricoma (PM; calcifying epithelioma of Malherbe) is an uncommon adnexal tumour originating from the matrix of the hair follicles. Bullous appearance is a rare variant of PM, and its pathogenesis remains unclear. Here, we present a case of a 17‐year‐old girl with a pseudobullous PM on the right...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435458/ https://www.ncbi.nlm.nih.gov/pubmed/36092264 http://dx.doi.org/10.1002/ski2.115 |
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author | Lee, Tung‐Chun Liu, Yan Zhang, Ya‐Mei Huang, Yike Wang, Zhi‐Yan Lu, Gui‐Qing |
author_facet | Lee, Tung‐Chun Liu, Yan Zhang, Ya‐Mei Huang, Yike Wang, Zhi‐Yan Lu, Gui‐Qing |
author_sort | Lee, Tung‐Chun |
collection | PubMed |
description | Pilomatricoma (PM; calcifying epithelioma of Malherbe) is an uncommon adnexal tumour originating from the matrix of the hair follicles. Bullous appearance is a rare variant of PM, and its pathogenesis remains unclear. Here, we present a case of a 17‐year‐old girl with a pseudobullous PM on the right shoulder. Lymphatic dilatation and collagen disorder were histopathologically observed in this case, which may provide clues to elucidate the pathogenesis of pseudobullous PM. |
format | Online Article Text |
id | pubmed-9435458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94354582022-09-08 Pseudobullous pilomatricoma: A rare variant of pilomatricoma Lee, Tung‐Chun Liu, Yan Zhang, Ya‐Mei Huang, Yike Wang, Zhi‐Yan Lu, Gui‐Qing Skin Health Dis Case Reports Pilomatricoma (PM; calcifying epithelioma of Malherbe) is an uncommon adnexal tumour originating from the matrix of the hair follicles. Bullous appearance is a rare variant of PM, and its pathogenesis remains unclear. Here, we present a case of a 17‐year‐old girl with a pseudobullous PM on the right shoulder. Lymphatic dilatation and collagen disorder were histopathologically observed in this case, which may provide clues to elucidate the pathogenesis of pseudobullous PM. John Wiley and Sons Inc. 2022-04-02 /pmc/articles/PMC9435458/ /pubmed/36092264 http://dx.doi.org/10.1002/ski2.115 Text en © 2022 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Lee, Tung‐Chun Liu, Yan Zhang, Ya‐Mei Huang, Yike Wang, Zhi‐Yan Lu, Gui‐Qing Pseudobullous pilomatricoma: A rare variant of pilomatricoma |
title | Pseudobullous pilomatricoma: A rare variant of pilomatricoma |
title_full | Pseudobullous pilomatricoma: A rare variant of pilomatricoma |
title_fullStr | Pseudobullous pilomatricoma: A rare variant of pilomatricoma |
title_full_unstemmed | Pseudobullous pilomatricoma: A rare variant of pilomatricoma |
title_short | Pseudobullous pilomatricoma: A rare variant of pilomatricoma |
title_sort | pseudobullous pilomatricoma: a rare variant of pilomatricoma |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435458/ https://www.ncbi.nlm.nih.gov/pubmed/36092264 http://dx.doi.org/10.1002/ski2.115 |
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