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A Case of Familial Cutaneous Collagenoma

Familial cutaneous collagenoma is a rare hereditary disease that is inherited in an autosomal dominant pattern. It is characterized by early onset of multiple, skin-colored, sometimes hypopigmented cutaneous nodules, which initially show a symmetrical arrangement on the trunk, and later on the neck...

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Autores principales: Park, Mi-Youn, Choi, Yeon-Jin, Lee, Jung-Yeon, Shin, Mi-Seon, Ahn, Ji-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199407/
https://www.ncbi.nlm.nih.gov/pubmed/22028557
http://dx.doi.org/10.5021/ad.2011.23.S1.S119
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author Park, Mi-Youn
Choi, Yeon-Jin
Lee, Jung-Yeon
Shin, Mi-Seon
Ahn, Ji-Young
author_facet Park, Mi-Youn
Choi, Yeon-Jin
Lee, Jung-Yeon
Shin, Mi-Seon
Ahn, Ji-Young
author_sort Park, Mi-Youn
collection PubMed
description Familial cutaneous collagenoma is a rare hereditary disease that is inherited in an autosomal dominant pattern. It is characterized by early onset of multiple, skin-colored, sometimes hypopigmented cutaneous nodules, which initially show a symmetrical arrangement on the trunk, and later on the neck and upper limbs. We report on a case of a 45-year-old female who presented with multiple oval to round hypopigmented papules measuring 5~15 mm on her trunk. Histopathologically, the lesions showed an increased amount of collagen fibers and decreased, fragmented elastic fibers in the dermis. The skin lesions were diagnosed as familial cutaneous collagenoma and no treatment was administered. To the best of our knowledge, our case is the first reported case of familial cutaneous collagenoma (FCC) in the Korean literature.
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spelling pubmed-31994072011-10-25 A Case of Familial Cutaneous Collagenoma Park, Mi-Youn Choi, Yeon-Jin Lee, Jung-Yeon Shin, Mi-Seon Ahn, Ji-Young Ann Dermatol Case Report Familial cutaneous collagenoma is a rare hereditary disease that is inherited in an autosomal dominant pattern. It is characterized by early onset of multiple, skin-colored, sometimes hypopigmented cutaneous nodules, which initially show a symmetrical arrangement on the trunk, and later on the neck and upper limbs. We report on a case of a 45-year-old female who presented with multiple oval to round hypopigmented papules measuring 5~15 mm on her trunk. Histopathologically, the lesions showed an increased amount of collagen fibers and decreased, fragmented elastic fibers in the dermis. The skin lesions were diagnosed as familial cutaneous collagenoma and no treatment was administered. To the best of our knowledge, our case is the first reported case of familial cutaneous collagenoma (FCC) in the Korean literature. Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011-09 2011-09-30 /pmc/articles/PMC3199407/ /pubmed/22028557 http://dx.doi.org/10.5021/ad.2011.23.S1.S119 Text en Copyright © 2011 Korean Dermatological Association; 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
Park, Mi-Youn
Choi, Yeon-Jin
Lee, Jung-Yeon
Shin, Mi-Seon
Ahn, Ji-Young
A Case of Familial Cutaneous Collagenoma
title A Case of Familial Cutaneous Collagenoma
title_full A Case of Familial Cutaneous Collagenoma
title_fullStr A Case of Familial Cutaneous Collagenoma
title_full_unstemmed A Case of Familial Cutaneous Collagenoma
title_short A Case of Familial Cutaneous Collagenoma
title_sort case of familial cutaneous collagenoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199407/
https://www.ncbi.nlm.nih.gov/pubmed/22028557
http://dx.doi.org/10.5021/ad.2011.23.S1.S119
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