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Pinch Purpura in Adult Colloid Milium—A Case Report
Colloid milium is a rare cutaneous deposition disorder characterized by the presence of asymptomatic multiple dome-shaped semi-translucent waxy yellowish or skin-colored papules. It is commonly seen on the face and dorsum of forearms and arms due to chronic sun exposure. Nodular amyloidosis and prim...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373808/ https://www.ncbi.nlm.nih.gov/pubmed/37521221 http://dx.doi.org/10.4103/idoj.idoj_466_22 |
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author | Krishnaram, AS Geetha, T SriRam, CK Shibani, MI Priya, Sri Krishna |
author_facet | Krishnaram, AS Geetha, T SriRam, CK Shibani, MI Priya, Sri Krishna |
author_sort | Krishnaram, AS |
collection | PubMed |
description | Colloid milium is a rare cutaneous deposition disorder characterized by the presence of asymptomatic multiple dome-shaped semi-translucent waxy yellowish or skin-colored papules. It is commonly seen on the face and dorsum of forearms and arms due to chronic sun exposure. Nodular amyloidosis and primary systemic amyloidosis mimic adult colloid milium more closely. They share indistinguishable common features clinically and histologically. Purpura following trivial injury is a cardinal feature of primary systemic amyloidosis. Here, we are reporting a case of adult colloid milium, presented with waxy papules and purpura involving the dorsa of the lower half of the forearms and hands which is confirmed by histopathological and immunohistochemical studies. |
format | Online Article Text |
id | pubmed-10373808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-103738082023-07-28 Pinch Purpura in Adult Colloid Milium—A Case Report Krishnaram, AS Geetha, T SriRam, CK Shibani, MI Priya, Sri Krishna Indian Dermatol Online J Case Report Colloid milium is a rare cutaneous deposition disorder characterized by the presence of asymptomatic multiple dome-shaped semi-translucent waxy yellowish or skin-colored papules. It is commonly seen on the face and dorsum of forearms and arms due to chronic sun exposure. Nodular amyloidosis and primary systemic amyloidosis mimic adult colloid milium more closely. They share indistinguishable common features clinically and histologically. Purpura following trivial injury is a cardinal feature of primary systemic amyloidosis. Here, we are reporting a case of adult colloid milium, presented with waxy papules and purpura involving the dorsa of the lower half of the forearms and hands which is confirmed by histopathological and immunohistochemical studies. Wolters Kluwer - Medknow 2023-05-25 /pmc/articles/PMC10373808/ /pubmed/37521221 http://dx.doi.org/10.4103/idoj.idoj_466_22 Text en Copyright: © 2023 Indian Dermatology Online Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Krishnaram, AS Geetha, T SriRam, CK Shibani, MI Priya, Sri Krishna Pinch Purpura in Adult Colloid Milium—A Case Report |
title | Pinch Purpura in Adult Colloid Milium—A Case Report |
title_full | Pinch Purpura in Adult Colloid Milium—A Case Report |
title_fullStr | Pinch Purpura in Adult Colloid Milium—A Case Report |
title_full_unstemmed | Pinch Purpura in Adult Colloid Milium—A Case Report |
title_short | Pinch Purpura in Adult Colloid Milium—A Case Report |
title_sort | pinch purpura in adult colloid milium—a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373808/ https://www.ncbi.nlm.nih.gov/pubmed/37521221 http://dx.doi.org/10.4103/idoj.idoj_466_22 |
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