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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2018
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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. |
format | Online Article Text |
id | pubmed-5871374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT jiangyuan atrophicnodularcutaneousamyloidosis AT kongqingtao atrophicnodularcutaneousamyloidosis AT huiyun atrophicnodularcutaneousamyloidosis AT sanghong atrophicnodularcutaneousamyloidosis |