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Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored
Eccrine angiomatous hamartoma (EAH) is a rare, benign, slow-growing cutaneous lesion characterized by hamartomatous proliferation of the eccrine glands and vascular structures. It usually arises in early childhood; however, cases in adults have also been reported. It is diagnosed based on the clinic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055288/ https://www.ncbi.nlm.nih.gov/pubmed/35505764 http://dx.doi.org/10.7759/cureus.23669 |
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author | Al-Zaidi, Rana S Alotaibi, Ghazwa Aljuaid, Mohammed |
author_facet | Al-Zaidi, Rana S Alotaibi, Ghazwa Aljuaid, Mohammed |
author_sort | Al-Zaidi, Rana S |
collection | PubMed |
description | Eccrine angiomatous hamartoma (EAH) is a rare, benign, slow-growing cutaneous lesion characterized by hamartomatous proliferation of the eccrine glands and vascular structures. It usually arises in early childhood; however, cases in adults have also been reported. It is diagnosed based on the clinical features of the lesion as well as the histopathological findings of the excised tissue. As the name indicates, EAH shows a close association with mature eccrine elements and capillary-sized blood vessels at the histopathological level. In rare instances, the vascular component can show the features of arteriovenous malformations. Here, we report a rare case of EAH with a component of arteriovenous malformation in a 39-year-old woman who presented with a foot lesion. |
format | Online Article Text |
id | pubmed-9055288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-90552882022-05-02 Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored Al-Zaidi, Rana S Alotaibi, Ghazwa Aljuaid, Mohammed Cureus Dermatology Eccrine angiomatous hamartoma (EAH) is a rare, benign, slow-growing cutaneous lesion characterized by hamartomatous proliferation of the eccrine glands and vascular structures. It usually arises in early childhood; however, cases in adults have also been reported. It is diagnosed based on the clinical features of the lesion as well as the histopathological findings of the excised tissue. As the name indicates, EAH shows a close association with mature eccrine elements and capillary-sized blood vessels at the histopathological level. In rare instances, the vascular component can show the features of arteriovenous malformations. Here, we report a rare case of EAH with a component of arteriovenous malformation in a 39-year-old woman who presented with a foot lesion. Cureus 2022-03-30 /pmc/articles/PMC9055288/ /pubmed/35505764 http://dx.doi.org/10.7759/cureus.23669 Text en Copyright © 2022, Al-Zaidi et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Dermatology Al-Zaidi, Rana S Alotaibi, Ghazwa Aljuaid, Mohammed Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored |
title | Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored |
title_full | Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored |
title_fullStr | Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored |
title_full_unstemmed | Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored |
title_short | Eccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored |
title_sort | eccrine angiomatous hamartoma with arteriovenous malformation: a rare entity re-explored |
topic | Dermatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055288/ https://www.ncbi.nlm.nih.gov/pubmed/35505764 http://dx.doi.org/10.7759/cureus.23669 |
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