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A rare case of granuloma faciale presenting with ulceration: A case report
Granuloma faciale is an uncommon inflammatory dermatosis characterized by persistent dermal plaques, typically on the face, that mimic granulomatous disorders like sarcoidosis. Ulceration of granuloma faciale has very rarely been reported, and the plaques are usually asymptomatic and of cosmetic imp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047788/ https://www.ncbi.nlm.nih.gov/pubmed/35495289 http://dx.doi.org/10.1177/2050313X221093150 |
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author | Mahmood, Farhan Teo, Iris YH Glassman, Steven J |
author_facet | Mahmood, Farhan Teo, Iris YH Glassman, Steven J |
author_sort | Mahmood, Farhan |
collection | PubMed |
description | Granuloma faciale is an uncommon inflammatory dermatosis characterized by persistent dermal plaques, typically on the face, that mimic granulomatous disorders like sarcoidosis. Ulceration of granuloma faciale has very rarely been reported, and the plaques are usually asymptomatic and of cosmetic impact. We present a case of an 83-year-old male with recurrent granuloma faciale with spontaneous ulceration and monoclonal gammopathy of undetermined significance. Intralesional triamcinolone, 10 mg/mL monthly for 5 months, with pimecrolimus cream twice daily resolved the ulceration and the lesion continues to flatten and lighten. Ulceration is rare and atypical in granuloma faciale lesions which can be treated. |
format | Online Article Text |
id | pubmed-9047788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-90477882022-04-29 A rare case of granuloma faciale presenting with ulceration: A case report Mahmood, Farhan Teo, Iris YH Glassman, Steven J SAGE Open Med Case Rep JCMS Case Report Granuloma faciale is an uncommon inflammatory dermatosis characterized by persistent dermal plaques, typically on the face, that mimic granulomatous disorders like sarcoidosis. Ulceration of granuloma faciale has very rarely been reported, and the plaques are usually asymptomatic and of cosmetic impact. We present a case of an 83-year-old male with recurrent granuloma faciale with spontaneous ulceration and monoclonal gammopathy of undetermined significance. Intralesional triamcinolone, 10 mg/mL monthly for 5 months, with pimecrolimus cream twice daily resolved the ulceration and the lesion continues to flatten and lighten. Ulceration is rare and atypical in granuloma faciale lesions which can be treated. SAGE Publications 2022-04-24 /pmc/articles/PMC9047788/ /pubmed/35495289 http://dx.doi.org/10.1177/2050313X221093150 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | JCMS Case Report Mahmood, Farhan Teo, Iris YH Glassman, Steven J A rare case of granuloma faciale presenting with ulceration: A case report |
title | A rare case of granuloma faciale presenting with ulceration: A case
report |
title_full | A rare case of granuloma faciale presenting with ulceration: A case
report |
title_fullStr | A rare case of granuloma faciale presenting with ulceration: A case
report |
title_full_unstemmed | A rare case of granuloma faciale presenting with ulceration: A case
report |
title_short | A rare case of granuloma faciale presenting with ulceration: A case
report |
title_sort | rare case of granuloma faciale presenting with ulceration: a case
report |
topic | JCMS Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047788/ https://www.ncbi.nlm.nih.gov/pubmed/35495289 http://dx.doi.org/10.1177/2050313X221093150 |
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