Syringocystadenoma papilliferum: case series and review of the literature

Syringocystadenoma papilliferum (SCAP) is a rare, hamartomatous tumor of the apocrine glands, which typically manifests in the head and neck region. We present a case of 60-year-old male with a several-year history of the lesion located on the abdominal wall and a second case of a 58-year-old male w...

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Autores principales: Gorji, Leva, Hamilton, Matthew, Reyes, Nicole M, O’Neill, Erin M, Floyd, Zachary R, Elrod, Michael A, Archer, Andrew L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198642/
https://www.ncbi.nlm.nih.gov/pubmed/37215626
http://dx.doi.org/10.1093/jscr/rjad263
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author Gorji, Leva
Hamilton, Matthew
Reyes, Nicole M
O’Neill, Erin M
Floyd, Zachary R
Elrod, Michael A
Archer, Andrew L
author_facet Gorji, Leva
Hamilton, Matthew
Reyes, Nicole M
O’Neill, Erin M
Floyd, Zachary R
Elrod, Michael A
Archer, Andrew L
author_sort Gorji, Leva
collection PubMed
description Syringocystadenoma papilliferum (SCAP) is a rare, hamartomatous tumor of the apocrine glands, which typically manifests in the head and neck region. We present a case of 60-year-old male with a several-year history of the lesion located on the abdominal wall and a second case of a 58-year-old male with a history of a slow-growing lesion located on the tragus. Despite varying presentations and locations, both patients were identified to have SCAP on pathological evaluation. Appropriate treatments of SCAP range from CO2 laser treatment to surgical excision; we recommend surgical excision due to the risk of malignant transformation.
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spelling pubmed-101986422023-05-20 Syringocystadenoma papilliferum: case series and review of the literature Gorji, Leva Hamilton, Matthew Reyes, Nicole M O’Neill, Erin M Floyd, Zachary R Elrod, Michael A Archer, Andrew L J Surg Case Rep Case Series Syringocystadenoma papilliferum (SCAP) is a rare, hamartomatous tumor of the apocrine glands, which typically manifests in the head and neck region. We present a case of 60-year-old male with a several-year history of the lesion located on the abdominal wall and a second case of a 58-year-old male with a history of a slow-growing lesion located on the tragus. Despite varying presentations and locations, both patients were identified to have SCAP on pathological evaluation. Appropriate treatments of SCAP range from CO2 laser treatment to surgical excision; we recommend surgical excision due to the risk of malignant transformation. Oxford University Press 2023-05-18 /pmc/articles/PMC10198642/ /pubmed/37215626 http://dx.doi.org/10.1093/jscr/rjad263 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Series
Gorji, Leva
Hamilton, Matthew
Reyes, Nicole M
O’Neill, Erin M
Floyd, Zachary R
Elrod, Michael A
Archer, Andrew L
Syringocystadenoma papilliferum: case series and review of the literature
title Syringocystadenoma papilliferum: case series and review of the literature
title_full Syringocystadenoma papilliferum: case series and review of the literature
title_fullStr Syringocystadenoma papilliferum: case series and review of the literature
title_full_unstemmed Syringocystadenoma papilliferum: case series and review of the literature
title_short Syringocystadenoma papilliferum: case series and review of the literature
title_sort syringocystadenoma papilliferum: case series and review of the literature
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198642/
https://www.ncbi.nlm.nih.gov/pubmed/37215626
http://dx.doi.org/10.1093/jscr/rjad263
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