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Atrophic Dermatofibroma in a Young Female: A Rare Entity
INTRODUCTION: Atrophic dermatofibroma is a rare variant of dermatofibroma which is many times underdiagnosed. CASE REPORT: We report a case report of a 29-year-old female who came to the dermatology department with black-colored lesions on the lower leg for the past 7 years. Histopathological examin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906261/ https://www.ncbi.nlm.nih.gov/pubmed/35283608 http://dx.doi.org/10.4103/JCAS.JCAS_100_20 |
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author | Puri, Neerja Brar, Balvinder Kaur Azhagappan, Anjugam |
author_facet | Puri, Neerja Brar, Balvinder Kaur Azhagappan, Anjugam |
author_sort | Puri, Neerja |
collection | PubMed |
description | INTRODUCTION: Atrophic dermatofibroma is a rare variant of dermatofibroma which is many times underdiagnosed. CASE REPORT: We report a case report of a 29-year-old female who came to the dermatology department with black-colored lesions on the lower leg for the past 7 years. Histopathological examination revealed a non-encapsulated dermal tumor involving upper to deep reticular dermis and extending to superficial subcutis. There was epidermal hyperplasia, and at the center of the lesion a slight epidermal atrophy was present. DISCUSSION: It is a commonly underdiagnosed variant of dermatofibroma. Histopathologically, this disorder presents as a decrease in at least 50% of the thickness of the dermis relative to the adjacent dermis. The case is rare and hence reported. |
format | Online Article Text |
id | pubmed-8906261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-89062612022-03-10 Atrophic Dermatofibroma in a Young Female: A Rare Entity Puri, Neerja Brar, Balvinder Kaur Azhagappan, Anjugam J Cutan Aesthet Surg Case Reports INTRODUCTION: Atrophic dermatofibroma is a rare variant of dermatofibroma which is many times underdiagnosed. CASE REPORT: We report a case report of a 29-year-old female who came to the dermatology department with black-colored lesions on the lower leg for the past 7 years. Histopathological examination revealed a non-encapsulated dermal tumor involving upper to deep reticular dermis and extending to superficial subcutis. There was epidermal hyperplasia, and at the center of the lesion a slight epidermal atrophy was present. DISCUSSION: It is a commonly underdiagnosed variant of dermatofibroma. Histopathologically, this disorder presents as a decrease in at least 50% of the thickness of the dermis relative to the adjacent dermis. The case is rare and hence reported. Wolters Kluwer - Medknow 2021 /pmc/articles/PMC8906261/ /pubmed/35283608 http://dx.doi.org/10.4103/JCAS.JCAS_100_20 Text en Copyright: © 2022 Journal of Cutaneous and Aesthetic Surgery 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 Reports Puri, Neerja Brar, Balvinder Kaur Azhagappan, Anjugam Atrophic Dermatofibroma in a Young Female: A Rare Entity |
title | Atrophic Dermatofibroma in a Young Female: A Rare Entity |
title_full | Atrophic Dermatofibroma in a Young Female: A Rare Entity |
title_fullStr | Atrophic Dermatofibroma in a Young Female: A Rare Entity |
title_full_unstemmed | Atrophic Dermatofibroma in a Young Female: A Rare Entity |
title_short | Atrophic Dermatofibroma in a Young Female: A Rare Entity |
title_sort | atrophic dermatofibroma in a young female: a rare entity |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906261/ https://www.ncbi.nlm.nih.gov/pubmed/35283608 http://dx.doi.org/10.4103/JCAS.JCAS_100_20 |
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