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Atrophic nodular cutaneous amyloidosis*

Primary cutaneous amyloidosis is limited to the skin without involving any other tissue. Nodular amyloidosis is rare, and atrophic nodular cutaneous amyloidosis is even rarer. We describe the fourth case of atrophic nodular cutaneous amyloidosis by searching PubMed databases. A 52-year-old female pr...

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Detalles Bibliográficos
Autores principales: Jiang, Yuan, kong, Qingtao, Hui, Yun, Sang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871374/
https://www.ncbi.nlm.nih.gov/pubmed/29641709
http://dx.doi.org/10.1590/abd1806-4841.20186504
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author Jiang, Yuan
kong, Qingtao
Hui, Yun
Sang, Hong
author_facet Jiang, Yuan
kong, Qingtao
Hui, Yun
Sang, Hong
author_sort Jiang, Yuan
collection PubMed
description Primary cutaneous amyloidosis is limited to the skin without involving any other tissue. Nodular amyloidosis is rare, and atrophic nodular cutaneous amyloidosis is even rarer. We describe the fourth case of atrophic nodular cutaneous amyloidosis by searching PubMed databases. A 52-year-old female presented to our hospital with a 2-year history of orange papules and nodules without subjective symptom on her right abdomen. Review of systems was negative. Atrophic nodular amyloidosis may progress to primary systemic disease in up to 7% of cases. Because our patient had no systemic involvement, she was diagnosed with atrophic nodular cutaneous amyloidosis based on characteristic symptoms and histopathologic examination. Routine follow-up for this patient is necessary to detect any potential disease progression.
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spelling pubmed-58713742018-03-29 Atrophic nodular cutaneous amyloidosis* Jiang, Yuan kong, Qingtao Hui, Yun Sang, Hong An Bras Dermatol Case Report Primary cutaneous amyloidosis is limited to the skin without involving any other tissue. Nodular amyloidosis is rare, and atrophic nodular cutaneous amyloidosis is even rarer. We describe the fourth case of atrophic nodular cutaneous amyloidosis by searching PubMed databases. A 52-year-old female presented to our hospital with a 2-year history of orange papules and nodules without subjective symptom on her right abdomen. Review of systems was negative. Atrophic nodular amyloidosis may progress to primary systemic disease in up to 7% of cases. Because our patient had no systemic involvement, she was diagnosed with atrophic nodular cutaneous amyloidosis based on characteristic symptoms and histopathologic examination. Routine follow-up for this patient is necessary to detect any potential disease progression. Sociedade Brasileira de Dermatologia 2018 /pmc/articles/PMC5871374/ /pubmed/29641709 http://dx.doi.org/10.1590/abd1806-4841.20186504 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivative License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way.
spellingShingle Case Report
Jiang, Yuan
kong, Qingtao
Hui, Yun
Sang, Hong
Atrophic nodular cutaneous amyloidosis*
title Atrophic nodular cutaneous amyloidosis*
title_full Atrophic nodular cutaneous amyloidosis*
title_fullStr Atrophic nodular cutaneous amyloidosis*
title_full_unstemmed Atrophic nodular cutaneous amyloidosis*
title_short Atrophic nodular cutaneous amyloidosis*
title_sort atrophic nodular cutaneous amyloidosis*
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871374/
https://www.ncbi.nlm.nih.gov/pubmed/29641709
http://dx.doi.org/10.1590/abd1806-4841.20186504
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