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Syringocystadenoma Papilliferum: A Case Report and Review of the Literature

Syringocystadenoma papilliferum is a very rare, benign adnexal tumor that originates from the apocrine sweat glands. Herein, we report a 25-year-old male who presented with a 10-year history of an asymptomatic slowly growing skin lesion on his face. Skin examination revealed a solitary rounded 3 × 3...

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Autores principales: Al Hawsawi, Khalid, Alharazi, Amani, Ashary, Abeer, Siddique, Asmaa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184794/
https://www.ncbi.nlm.nih.gov/pubmed/32355486
http://dx.doi.org/10.1159/000497054
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author Al Hawsawi, Khalid
Alharazi, Amani
Ashary, Abeer
Siddique, Asmaa
author_facet Al Hawsawi, Khalid
Alharazi, Amani
Ashary, Abeer
Siddique, Asmaa
author_sort Al Hawsawi, Khalid
collection PubMed
description Syringocystadenoma papilliferum is a very rare, benign adnexal tumor that originates from the apocrine sweat glands. Herein, we report a 25-year-old male who presented with a 10-year history of an asymptomatic slowly growing skin lesion on his face. Skin examination revealed a solitary rounded 3 × 3 cm erythematous plaque with central crustation on the right side of his face. Punch skin biopsy was taken from the lesion. The epidermis showed downward papillomatous extensions. The dermis showed multiple epithelial sheets and dilated ducts that were lined by columnar cells. On the basis of the above clinicopathological findings, the diagnosis of syringocystadenoma papilliferum was made. The patient was reassured and referred to a surgeon for surgical excision of the lesion.
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spelling pubmed-71847942020-04-30 Syringocystadenoma Papilliferum: A Case Report and Review of the Literature Al Hawsawi, Khalid Alharazi, Amani Ashary, Abeer Siddique, Asmaa Case Rep Dermatol Single Case Syringocystadenoma papilliferum is a very rare, benign adnexal tumor that originates from the apocrine sweat glands. Herein, we report a 25-year-old male who presented with a 10-year history of an asymptomatic slowly growing skin lesion on his face. Skin examination revealed a solitary rounded 3 × 3 cm erythematous plaque with central crustation on the right side of his face. Punch skin biopsy was taken from the lesion. The epidermis showed downward papillomatous extensions. The dermis showed multiple epithelial sheets and dilated ducts that were lined by columnar cells. On the basis of the above clinicopathological findings, the diagnosis of syringocystadenoma papilliferum was made. The patient was reassured and referred to a surgeon for surgical excision of the lesion. S. Karger AG 2019-02-14 /pmc/articles/PMC7184794/ /pubmed/32355486 http://dx.doi.org/10.1159/000497054 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case
Al Hawsawi, Khalid
Alharazi, Amani
Ashary, Abeer
Siddique, Asmaa
Syringocystadenoma Papilliferum: A Case Report and Review of the Literature
title Syringocystadenoma Papilliferum: A Case Report and Review of the Literature
title_full Syringocystadenoma Papilliferum: A Case Report and Review of the Literature
title_fullStr Syringocystadenoma Papilliferum: A Case Report and Review of the Literature
title_full_unstemmed Syringocystadenoma Papilliferum: A Case Report and Review of the Literature
title_short Syringocystadenoma Papilliferum: A Case Report and Review of the Literature
title_sort syringocystadenoma papilliferum: a case report and review of the literature
topic Single Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184794/
https://www.ncbi.nlm.nih.gov/pubmed/32355486
http://dx.doi.org/10.1159/000497054
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