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Livedoid vasculopathy: A review with focus on terminology and pathogenesis

Livedoid vasculopathy (LV) is a rare thrombotic vasculopathy of the dermis characterized by painful, relapsing ulcers over the lower extremities. Diagnosis is challenging due to the overlap in clinical appearance and nomenclature with other skin disorders. Treatment selection is complicated by poor...

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Autores principales: Eswaran, Harish, Googe, Paul, Vedak, Priyanka, Marston, William A, Moll, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732787/
https://www.ncbi.nlm.nih.gov/pubmed/36285834
http://dx.doi.org/10.1177/1358863X221130380
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author Eswaran, Harish
Googe, Paul
Vedak, Priyanka
Marston, William A
Moll, Stephan
author_facet Eswaran, Harish
Googe, Paul
Vedak, Priyanka
Marston, William A
Moll, Stephan
author_sort Eswaran, Harish
collection PubMed
description Livedoid vasculopathy (LV) is a rare thrombotic vasculopathy of the dermis characterized by painful, relapsing ulcers over the lower extremities. Diagnosis is challenging due to the overlap in clinical appearance and nomenclature with other skin disorders. Treatment selection is complicated by poor understanding of the pathogenesis of LV and lack of robust clinical trials evaluating therapy efficacy. The terminology and pathophysiology of LV are reviewed here, along with its epidemiology, clinical and histologic features, and treatment options. A diagnostic pathway is suggested to guide providers in evaluating for comorbidities, referring to appropriate specialists, and choosing from the available classes of therapy.
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spelling pubmed-97327872022-12-10 Livedoid vasculopathy: A review with focus on terminology and pathogenesis Eswaran, Harish Googe, Paul Vedak, Priyanka Marston, William A Moll, Stephan Vasc Med Review: Core Curriculum in Vascular Medicine Livedoid vasculopathy (LV) is a rare thrombotic vasculopathy of the dermis characterized by painful, relapsing ulcers over the lower extremities. Diagnosis is challenging due to the overlap in clinical appearance and nomenclature with other skin disorders. Treatment selection is complicated by poor understanding of the pathogenesis of LV and lack of robust clinical trials evaluating therapy efficacy. The terminology and pathophysiology of LV are reviewed here, along with its epidemiology, clinical and histologic features, and treatment options. A diagnostic pathway is suggested to guide providers in evaluating for comorbidities, referring to appropriate specialists, and choosing from the available classes of therapy. SAGE Publications 2022-10-26 2022-12 /pmc/articles/PMC9732787/ /pubmed/36285834 http://dx.doi.org/10.1177/1358863X221130380 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 Review: Core Curriculum in Vascular Medicine
Eswaran, Harish
Googe, Paul
Vedak, Priyanka
Marston, William A
Moll, Stephan
Livedoid vasculopathy: A review with focus on terminology and pathogenesis
title Livedoid vasculopathy: A review with focus on terminology and pathogenesis
title_full Livedoid vasculopathy: A review with focus on terminology and pathogenesis
title_fullStr Livedoid vasculopathy: A review with focus on terminology and pathogenesis
title_full_unstemmed Livedoid vasculopathy: A review with focus on terminology and pathogenesis
title_short Livedoid vasculopathy: A review with focus on terminology and pathogenesis
title_sort livedoid vasculopathy: a review with focus on terminology and pathogenesis
topic Review: Core Curriculum in Vascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732787/
https://www.ncbi.nlm.nih.gov/pubmed/36285834
http://dx.doi.org/10.1177/1358863X221130380
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