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Nodular Cutaneous Amyloidosis Resembling a Giant Tumor

A 79-year-old man presented with a large tumor on the left side of his head, which had grown over 5 years. Regional lymph nodes were impalpable and computed tomography revealed no signs of bone infiltration. Histology showed that the entire dermis was filled with amorphous eosinophilic material. Imm...

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Autores principales: Haverkampf, Sonja, Evert, Katja, Schröder, Josef, Schreml, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899645/
https://www.ncbi.nlm.nih.gov/pubmed/27293389
http://dx.doi.org/10.1159/000443950
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author Haverkampf, Sonja
Evert, Katja
Schröder, Josef
Schreml, Stephan
author_facet Haverkampf, Sonja
Evert, Katja
Schröder, Josef
Schreml, Stephan
author_sort Haverkampf, Sonja
collection PubMed
description A 79-year-old man presented with a large tumor on the left side of his head, which had grown over 5 years. Regional lymph nodes were impalpable and computed tomography revealed no signs of bone infiltration. Histology showed that the entire dermis was filled with amorphous eosinophilic material. Immunohistochemistry was negative for cytokeratin, but showed that the dermis and parts of the subcutis were filled with amyloid consisting of immunoglobulin light chains. There were no signs of paraproteinemia or underlying plasmocytoma. In electron microscopy, the typical amyloid fibrils were found. The tumor was completely removed via curettage. At 1-year follow-up, the patient was doing fine with no signs of relapse or systemic disease.
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spelling pubmed-48996452016-06-10 Nodular Cutaneous Amyloidosis Resembling a Giant Tumor Haverkampf, Sonja Evert, Katja Schröder, Josef Schreml, Stephan Case Rep Dermatol Published online: February, 2016 A 79-year-old man presented with a large tumor on the left side of his head, which had grown over 5 years. Regional lymph nodes were impalpable and computed tomography revealed no signs of bone infiltration. Histology showed that the entire dermis was filled with amorphous eosinophilic material. Immunohistochemistry was negative for cytokeratin, but showed that the dermis and parts of the subcutis were filled with amyloid consisting of immunoglobulin light chains. There were no signs of paraproteinemia or underlying plasmocytoma. In electron microscopy, the typical amyloid fibrils were found. The tumor was completely removed via curettage. At 1-year follow-up, the patient was doing fine with no signs of relapse or systemic disease. S. Karger AG 2016-02-03 /pmc/articles/PMC4899645/ /pubmed/27293389 http://dx.doi.org/10.1159/000443950 Text en Copyright © 2016 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 Published online: February, 2016
Haverkampf, Sonja
Evert, Katja
Schröder, Josef
Schreml, Stephan
Nodular Cutaneous Amyloidosis Resembling a Giant Tumor
title Nodular Cutaneous Amyloidosis Resembling a Giant Tumor
title_full Nodular Cutaneous Amyloidosis Resembling a Giant Tumor
title_fullStr Nodular Cutaneous Amyloidosis Resembling a Giant Tumor
title_full_unstemmed Nodular Cutaneous Amyloidosis Resembling a Giant Tumor
title_short Nodular Cutaneous Amyloidosis Resembling a Giant Tumor
title_sort nodular cutaneous amyloidosis resembling a giant tumor
topic Published online: February, 2016
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899645/
https://www.ncbi.nlm.nih.gov/pubmed/27293389
http://dx.doi.org/10.1159/000443950
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