Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years

BACKGROUND: Cutis marmorata telangiectatic congenital or Van Lohuizen syndrome is a rare vascular disorder that may be associated with other congenital malformations. Around 300 cases have been reported so far. CASE REPORT: We present a 4-year-old girl with Van Lohuizen syndrome of the leg, but with...

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Autores principales: Wollina, Uwe, França, Katlein, Lotti, Torello, Tchernev, Georgi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Republic of Macedonia 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816322/
https://www.ncbi.nlm.nih.gov/pubmed/29483988
http://dx.doi.org/10.3889/oamjms.2018.024
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author Wollina, Uwe
França, Katlein
Lotti, Torello
Tchernev, Georgi
author_facet Wollina, Uwe
França, Katlein
Lotti, Torello
Tchernev, Georgi
author_sort Wollina, Uwe
collection PubMed
description BACKGROUND: Cutis marmorata telangiectatic congenital or Van Lohuizen syndrome is a rare vascular disorder that may be associated with other congenital malformations. Around 300 cases have been reported so far. CASE REPORT: We present a 4-year-old girl with Van Lohuizen syndrome of the leg, but without any other malformations. CONCLUSION: Neonatal lupus erythematosus may resemble congenital vasculopathy, but histopathology and immune-serology are characteristic.
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spelling pubmed-58163222018-02-26 Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years Wollina, Uwe França, Katlein Lotti, Torello Tchernev, Georgi Open Access Maced J Med Sci Case Report BACKGROUND: Cutis marmorata telangiectatic congenital or Van Lohuizen syndrome is a rare vascular disorder that may be associated with other congenital malformations. Around 300 cases have been reported so far. CASE REPORT: We present a 4-year-old girl with Van Lohuizen syndrome of the leg, but without any other malformations. CONCLUSION: Neonatal lupus erythematosus may resemble congenital vasculopathy, but histopathology and immune-serology are characteristic. Republic of Macedonia 2018-01-02 /pmc/articles/PMC5816322/ /pubmed/29483988 http://dx.doi.org/10.3889/oamjms.2018.024 Text en Copyright: © 2018 Uwe Wollina, Katlein França, Torello Lotti, Georgi Tchernev. http://creativecommons.org/licenses/CC BY-NC/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
spellingShingle Case Report
Wollina, Uwe
França, Katlein
Lotti, Torello
Tchernev, Georgi
Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years
title Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years
title_full Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years
title_fullStr Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years
title_full_unstemmed Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years
title_short Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years
title_sort van lohuizen syndrome – a case report with a diagnostic delay of four years
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816322/
https://www.ncbi.nlm.nih.gov/pubmed/29483988
http://dx.doi.org/10.3889/oamjms.2018.024
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