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Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties
Pyoderma gangrenosum (PG) is a relatively rare neutrophilic dermatosis, characterized by progressive skin necrosis. It typically has a chronic course, of unknown etiology. Pyoderma gangrenosum diagnosis can be difficult because both histopathological examination and results of additional laboratory...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360003/ https://www.ncbi.nlm.nih.gov/pubmed/25821427 http://dx.doi.org/10.5114/pdia.2014.40947 |
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author | Wcisło-Dziadecka, Dominika Bergler-Czop, Beata Brzezińska-Wcisło, Ligia Arasiewicz, Hubert |
author_facet | Wcisło-Dziadecka, Dominika Bergler-Czop, Beata Brzezińska-Wcisło, Ligia Arasiewicz, Hubert |
author_sort | Wcisło-Dziadecka, Dominika |
collection | PubMed |
description | Pyoderma gangrenosum (PG) is a relatively rare neutrophilic dermatosis, characterized by progressive skin necrosis. It typically has a chronic course, of unknown etiology. Pyoderma gangrenosum diagnosis can be difficult because both histopathological examination and results of additional laboratory tests are not specific and the clinical state is conclusive, as for other physicians it poses a number of diagnostic dilemmas. Therefore, this condition should be treated interdisciplinary. We present a case of a 40-year-old patient with a diagnosis of PG, which in the early stages of the disease was treated as an extensive phlegmon by physicians of other specialties and it presented a serious diagnostic as well as therapeutic problem. |
format | Online Article Text |
id | pubmed-4360003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-43600032015-03-27 Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties Wcisło-Dziadecka, Dominika Bergler-Czop, Beata Brzezińska-Wcisło, Ligia Arasiewicz, Hubert Postepy Dermatol Alergol Case Report Pyoderma gangrenosum (PG) is a relatively rare neutrophilic dermatosis, characterized by progressive skin necrosis. It typically has a chronic course, of unknown etiology. Pyoderma gangrenosum diagnosis can be difficult because both histopathological examination and results of additional laboratory tests are not specific and the clinical state is conclusive, as for other physicians it poses a number of diagnostic dilemmas. Therefore, this condition should be treated interdisciplinary. We present a case of a 40-year-old patient with a diagnosis of PG, which in the early stages of the disease was treated as an extensive phlegmon by physicians of other specialties and it presented a serious diagnostic as well as therapeutic problem. Termedia Publishing House 2015-02-04 2015-02 /pmc/articles/PMC4360003/ /pubmed/25821427 http://dx.doi.org/10.5114/pdia.2014.40947 Text en Copyright © 2015 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Wcisło-Dziadecka, Dominika Bergler-Czop, Beata Brzezińska-Wcisło, Ligia Arasiewicz, Hubert Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
title | Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
title_full | Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
title_fullStr | Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
title_full_unstemmed | Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
title_short | Extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
title_sort | extensive phlegmon and pyoderma gangrenosum: diagnostic difficulties |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360003/ https://www.ncbi.nlm.nih.gov/pubmed/25821427 http://dx.doi.org/10.5114/pdia.2014.40947 |
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