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Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus

Epidermal nevi (EN) are hamartomatous lesions derived from epidermal components originating from pluripotent cell mutations. They have been categorized according to their predominant component. The existence of >2 types of EN concurrently within a single area or within contiguous areas has been r...

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Autores principales: Jung, Han Jin, Cha, Hyun Wuk, Lim, Hyun Jung, Lee, Seok-Jong, Kim, Do Won, Lee, Weon Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135107/
https://www.ncbi.nlm.nih.gov/pubmed/25143681
http://dx.doi.org/10.5021/ad.2014.26.4.501
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author Jung, Han Jin
Cha, Hyun Wuk
Lim, Hyun Jung
Lee, Seok-Jong
Kim, Do Won
Lee, Weon Ju
author_facet Jung, Han Jin
Cha, Hyun Wuk
Lim, Hyun Jung
Lee, Seok-Jong
Kim, Do Won
Lee, Weon Ju
author_sort Jung, Han Jin
collection PubMed
description Epidermal nevi (EN) are hamartomatous lesions derived from epidermal components originating from pluripotent cell mutations. They have been categorized according to their predominant component. The existence of >2 types of EN concurrently within a single area or within contiguous areas has been rarely reported. This report describes the case of simultaneous presence of a yellowish plaque on the left medial canthus and an aggregation of closed comedo-like papules on the right side of the cheek of a 15-year-old girl.
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spelling pubmed-41351072014-08-20 Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus Jung, Han Jin Cha, Hyun Wuk Lim, Hyun Jung Lee, Seok-Jong Kim, Do Won Lee, Weon Ju Ann Dermatol Case Report Epidermal nevi (EN) are hamartomatous lesions derived from epidermal components originating from pluripotent cell mutations. They have been categorized according to their predominant component. The existence of >2 types of EN concurrently within a single area or within contiguous areas has been rarely reported. This report describes the case of simultaneous presence of a yellowish plaque on the left medial canthus and an aggregation of closed comedo-like papules on the right side of the cheek of a 15-year-old girl. Korean Dermatological Association; The Korean Society for Investigative Dermatology 2014-08 2014-07-31 /pmc/articles/PMC4135107/ /pubmed/25143681 http://dx.doi.org/10.5021/ad.2014.26.4.501 Text en Copyright © 2014 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jung, Han Jin
Cha, Hyun Wuk
Lim, Hyun Jung
Lee, Seok-Jong
Kim, Do Won
Lee, Weon Ju
Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus
title Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus
title_full Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus
title_fullStr Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus
title_full_unstemmed Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus
title_short Two Concurrent Facial Epidermal Nevi without Systemic Abnormalities: Nevus Sebaceus and Nevus Comedonicus
title_sort two concurrent facial epidermal nevi without systemic abnormalities: nevus sebaceus and nevus comedonicus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135107/
https://www.ncbi.nlm.nih.gov/pubmed/25143681
http://dx.doi.org/10.5021/ad.2014.26.4.501
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