Primary Cutaneous Amyloidoma: A Case Report

Amyloidoma is defined as solitary, localized, tumor-like deposit of amyloid in diverse organs without evidence of systemic amyloidosis. Here we report the case of a 49-year-old male patient with a solitary amyloidoma of the skin seated on the left upper lip. Full medical examination showed no signs...

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Autores principales: Reitboeck, Julia García, Feldmann, Robert, Loader, Dagmara, Breier, Friedrich, Steiner, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2014
Materias:
Published online: November, 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264485/
https://www.ncbi.nlm.nih.gov/pubmed/25520648
http://dx.doi.org/10.1159/000369245
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author Reitboeck, Julia García
Feldmann, Robert
Loader, Dagmara
Breier, Friedrich
Steiner, Andreas
author_facet Reitboeck, Julia García
Feldmann, Robert
Loader, Dagmara
Breier, Friedrich
Steiner, Andreas
author_sort Reitboeck, Julia García
collection PubMed
description Amyloidoma is defined as solitary, localized, tumor-like deposit of amyloid in diverse organs without evidence of systemic amyloidosis. Here we report the case of a 49-year-old male patient with a solitary amyloidoma of the skin seated on the left upper lip. Full medical examination showed no signs of systemic amyloidosis. The mass was removed surgically with tangential shave and so far no signs of recurrence have been found.
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spelling pubmed-42644852014-12-17 Primary Cutaneous Amyloidoma: A Case Report Reitboeck, Julia García Feldmann, Robert Loader, Dagmara Breier, Friedrich Steiner, Andreas Case Rep Dermatol Published online: November, 2014 Amyloidoma is defined as solitary, localized, tumor-like deposit of amyloid in diverse organs without evidence of systemic amyloidosis. Here we report the case of a 49-year-old male patient with a solitary amyloidoma of the skin seated on the left upper lip. Full medical examination showed no signs of systemic amyloidosis. The mass was removed surgically with tangential shave and so far no signs of recurrence have been found. S. Karger AG 2014-11-14 /pmc/articles/PMC4264485/ /pubmed/25520648 http://dx.doi.org/10.1159/000369245 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: November, 2014
Reitboeck, Julia García
Feldmann, Robert
Loader, Dagmara
Breier, Friedrich
Steiner, Andreas
Primary Cutaneous Amyloidoma: A Case Report
title Primary Cutaneous Amyloidoma: A Case Report
title_full Primary Cutaneous Amyloidoma: A Case Report
title_fullStr Primary Cutaneous Amyloidoma: A Case Report
title_full_unstemmed Primary Cutaneous Amyloidoma: A Case Report
title_short Primary Cutaneous Amyloidoma: A Case Report
title_sort primary cutaneous amyloidoma: a case report
topic Published online: November, 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264485/
https://www.ncbi.nlm.nih.gov/pubmed/25520648
http://dx.doi.org/10.1159/000369245
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AT feldmannrobert primarycutaneousamyloidomaacasereport
AT loaderdagmara primarycutaneousamyloidomaacasereport
AT breierfriedrich primarycutaneousamyloidomaacasereport
AT steinerandreas primarycutaneousamyloidomaacasereport

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