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Pigmented Purpuric Dermatoses: A Complete Narrative Review

Pigmented purpuric dermatoses (PPD) include several skin diseases characterized by multiple petechial hemorrhage as consequence of capillaritis. PPD generally present with red to purple macules that progressively evolve to golden-brown color as the hemosiderin is reabsorbed. These lesions, often asy...

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Autores principales: Spigariolo, Cristina B., Giacalone, Serena, Nazzaro, Gianluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197337/
https://www.ncbi.nlm.nih.gov/pubmed/34070260
http://dx.doi.org/10.3390/jcm10112283
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author Spigariolo, Cristina B.
Giacalone, Serena
Nazzaro, Gianluca
author_facet Spigariolo, Cristina B.
Giacalone, Serena
Nazzaro, Gianluca
author_sort Spigariolo, Cristina B.
collection PubMed
description Pigmented purpuric dermatoses (PPD) include several skin diseases characterized by multiple petechial hemorrhage as consequence of capillaritis. PPD generally present with red to purple macules that progressively evolve to golden-brown color as the hemosiderin is reabsorbed. These lesions, often asymptomatic or associated with mild pruritus, usually occur on the lower extremities and may be a diagnostic and therapeutic challenge both for general practitioners and specialists in internal medicine or flebology. Clinical presentations include many subtypes that have been described over the years, although histology is usually superimposable. Prompt recognition and patient reassurance on the benign nature of these diseases is crucial. In this comprehensive review, we focused on pathogenesis and clinical pictures.
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spelling pubmed-81973372021-06-13 Pigmented Purpuric Dermatoses: A Complete Narrative Review Spigariolo, Cristina B. Giacalone, Serena Nazzaro, Gianluca J Clin Med Review Pigmented purpuric dermatoses (PPD) include several skin diseases characterized by multiple petechial hemorrhage as consequence of capillaritis. PPD generally present with red to purple macules that progressively evolve to golden-brown color as the hemosiderin is reabsorbed. These lesions, often asymptomatic or associated with mild pruritus, usually occur on the lower extremities and may be a diagnostic and therapeutic challenge both for general practitioners and specialists in internal medicine or flebology. Clinical presentations include many subtypes that have been described over the years, although histology is usually superimposable. Prompt recognition and patient reassurance on the benign nature of these diseases is crucial. In this comprehensive review, we focused on pathogenesis and clinical pictures. MDPI 2021-05-25 /pmc/articles/PMC8197337/ /pubmed/34070260 http://dx.doi.org/10.3390/jcm10112283 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Spigariolo, Cristina B.
Giacalone, Serena
Nazzaro, Gianluca
Pigmented Purpuric Dermatoses: A Complete Narrative Review
title Pigmented Purpuric Dermatoses: A Complete Narrative Review
title_full Pigmented Purpuric Dermatoses: A Complete Narrative Review
title_fullStr Pigmented Purpuric Dermatoses: A Complete Narrative Review
title_full_unstemmed Pigmented Purpuric Dermatoses: A Complete Narrative Review
title_short Pigmented Purpuric Dermatoses: A Complete Narrative Review
title_sort pigmented purpuric dermatoses: a complete narrative review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197337/
https://www.ncbi.nlm.nih.gov/pubmed/34070260
http://dx.doi.org/10.3390/jcm10112283
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