Multiple painful brownish plaques associated with local hyperphidrosis

Eccrine angiomatous hamartoma is a rare hamartomatous lesion characterized by proliferation of eccrine glands and small blood vessels, and occasionally other elements. It generally arises congenitally or later in childhood, as solitary or multiple lesions on the distal extremities. Adult-onset mult...

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Autores principales:	Nilay Duman, Gül Erkin, Nilgün Atakan, Özay Gököz
Formato:	article
Lenguaje:	EN
Publicado:	Mattioli1885 2015
Materias:	hyperhidrosis eccrine gland hamartoma Dermatology RL1-803
Acceso en línea:	https://doaj.org/article/ac7d1ba131354159a82569a54c69ac0d
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spelling	oai:doaj.org-article:ac7d1ba131354159a82569a54c69ac0d2021-11-17T08:31:48ZMultiple painful brownish plaques associated with local hyperphidrosis10.5826/dpc.0501a172160-9381https://doaj.org/article/ac7d1ba131354159a82569a54c69ac0d2015-01-01T00:00:00Zhttp://dpcj.org/index.php/dpc/article/view/864https://doaj.org/toc/2160-9381 Eccrine angiomatous hamartoma is a rare hamartomatous lesion characterized by proliferation of eccrine glands and small blood vessels, and occasionally other elements. It generally arises congenitally or later in childhood, as solitary or multiple lesions on the distal extremities. Adult-onset multiple lesions are very rare. Herein we describe a 33-year-old male with symptomatic multiple eccrine angiomatous hamartoma lesions. Nilay DumanGül ErkinNilgün AtakanÖzay GöközMattioli1885articlehyperhidrosiseccrine glandhamartomaDermatologyRL1-803ENDermatology Practical & Conceptual (2015)
institution	DOAJ
collection	DOAJ
language	EN
topic	hyperhidrosis eccrine gland hamartoma Dermatology RL1-803
spellingShingle	hyperhidrosis eccrine gland hamartoma Dermatology RL1-803 Nilay Duman Gül Erkin Nilgün Atakan Özay Gököz Multiple painful brownish plaques associated with local hyperphidrosis
description	Eccrine angiomatous hamartoma is a rare hamartomatous lesion characterized by proliferation of eccrine glands and small blood vessels, and occasionally other elements. It generally arises congenitally or later in childhood, as solitary or multiple lesions on the distal extremities. Adult-onset multiple lesions are very rare. Herein we describe a 33-year-old male with symptomatic multiple eccrine angiomatous hamartoma lesions.
format	article
author	Nilay Duman Gül Erkin Nilgün Atakan Özay Gököz
author_facet	Nilay Duman Gül Erkin Nilgün Atakan Özay Gököz
author_sort	Nilay Duman
title	Multiple painful brownish plaques associated with local hyperphidrosis
title_short	Multiple painful brownish plaques associated with local hyperphidrosis
title_full	Multiple painful brownish plaques associated with local hyperphidrosis
title_fullStr	Multiple painful brownish plaques associated with local hyperphidrosis
title_full_unstemmed	Multiple painful brownish plaques associated with local hyperphidrosis
title_sort	multiple painful brownish plaques associated with local hyperphidrosis
publisher	Mattioli1885
publishDate	2015
url	https://doaj.org/article/ac7d1ba131354159a82569a54c69ac0d
work_keys_str_mv	AT nilayduman multiplepainfulbrownishplaquesassociatedwithlocalhyperphidrosis AT gulerkin multiplepainfulbrownishplaquesassociatedwithlocalhyperphidrosis AT nilgunatakan multiplepainfulbrownishplaquesassociatedwithlocalhyperphidrosis AT ozaygokoz multiplepainfulbrownishplaquesassociatedwithlocalhyperphidrosis
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Multiple painful brownish plaques associated with local hyperphidrosis

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