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A Case of Nonuremic Calciphylaxis in a Caucasian Woman
We report a case of nonuremic calcific arteriolopathy (NUCA) in an 82-year-old Caucasian woman from rural Australia. The patient had no history of kidney disease or dialysis. NUCA is rare disease suspected on cutaneous and clinical features and diagnosed by characteristic findings on skin biopsy and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278186/ https://www.ncbi.nlm.nih.gov/pubmed/28191356 http://dx.doi.org/10.1155/2017/6831703 |
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author | Fergie, Bonnie Valecha, Nishant Miller, Andrew |
author_facet | Fergie, Bonnie Valecha, Nishant Miller, Andrew |
author_sort | Fergie, Bonnie |
collection | PubMed |
description | We report a case of nonuremic calcific arteriolopathy (NUCA) in an 82-year-old Caucasian woman from rural Australia. The patient had no history of kidney disease or dialysis. NUCA is rare disease suspected on cutaneous and clinical features and diagnosed by characteristic findings on skin biopsy and vasculature imaging. Calcification induced microvascular occlusion in the absence of renal failure may not be immediately apparent. Clinical suspicion and appropriate investigations are essential for making a diagnosis. A diagnosis of NUCA may be missed given the rarity of the disease, and dermatologists and patients alike would benefit from a greater awareness of this disease. |
format | Online Article Text |
id | pubmed-5278186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-52781862017-02-12 A Case of Nonuremic Calciphylaxis in a Caucasian Woman Fergie, Bonnie Valecha, Nishant Miller, Andrew Case Rep Dermatol Med Case Report We report a case of nonuremic calcific arteriolopathy (NUCA) in an 82-year-old Caucasian woman from rural Australia. The patient had no history of kidney disease or dialysis. NUCA is rare disease suspected on cutaneous and clinical features and diagnosed by characteristic findings on skin biopsy and vasculature imaging. Calcification induced microvascular occlusion in the absence of renal failure may not be immediately apparent. Clinical suspicion and appropriate investigations are essential for making a diagnosis. A diagnosis of NUCA may be missed given the rarity of the disease, and dermatologists and patients alike would benefit from a greater awareness of this disease. Hindawi Publishing Corporation 2017 2017-01-16 /pmc/articles/PMC5278186/ /pubmed/28191356 http://dx.doi.org/10.1155/2017/6831703 Text en Copyright © 2017 Bonnie Fergie et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Fergie, Bonnie Valecha, Nishant Miller, Andrew A Case of Nonuremic Calciphylaxis in a Caucasian Woman |
title | A Case of Nonuremic Calciphylaxis in a Caucasian Woman |
title_full | A Case of Nonuremic Calciphylaxis in a Caucasian Woman |
title_fullStr | A Case of Nonuremic Calciphylaxis in a Caucasian Woman |
title_full_unstemmed | A Case of Nonuremic Calciphylaxis in a Caucasian Woman |
title_short | A Case of Nonuremic Calciphylaxis in a Caucasian Woman |
title_sort | case of nonuremic calciphylaxis in a caucasian woman |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278186/ https://www.ncbi.nlm.nih.gov/pubmed/28191356 http://dx.doi.org/10.1155/2017/6831703 |
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