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An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report

BACKGROUND: Klippel-Trénaunay syndrome (KTS) is a rare congenital condition characterized by the clinical triad of capillary malformations (port wine stains), varicose veins with or without venous malformations, and bony and/or soft tissue hypertrophy. CASE PRESENTATION: Here we report the first cas...

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Autores principales: Al-Najjar, Rawan M., Fonseca, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451243/
https://www.ncbi.nlm.nih.gov/pubmed/30954069
http://dx.doi.org/10.1186/s12887-019-1480-0
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author Al-Najjar, Rawan M.
Fonseca, Rafael
author_facet Al-Najjar, Rawan M.
Fonseca, Rafael
author_sort Al-Najjar, Rawan M.
collection PubMed
description BACKGROUND: Klippel-Trénaunay syndrome (KTS) is a rare congenital condition characterized by the clinical triad of capillary malformations (port wine stains), varicose veins with or without venous malformations, and bony and/or soft tissue hypertrophy. CASE PRESENTATION: Here we report the first case of a one-day-old male with KTS presenting with crossed-bilateral limb hypertrophy and post-axial polydactyly. CONCLUSION: This case serves to highlight the variable presentation and multiple problems faced by patients with KTS and why multidisciplinary management is mandatory.
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spelling pubmed-64512432019-04-16 An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report Al-Najjar, Rawan M. Fonseca, Rafael BMC Pediatr Case Report BACKGROUND: Klippel-Trénaunay syndrome (KTS) is a rare congenital condition characterized by the clinical triad of capillary malformations (port wine stains), varicose veins with or without venous malformations, and bony and/or soft tissue hypertrophy. CASE PRESENTATION: Here we report the first case of a one-day-old male with KTS presenting with crossed-bilateral limb hypertrophy and post-axial polydactyly. CONCLUSION: This case serves to highlight the variable presentation and multiple problems faced by patients with KTS and why multidisciplinary management is mandatory. BioMed Central 2019-04-06 /pmc/articles/PMC6451243/ /pubmed/30954069 http://dx.doi.org/10.1186/s12887-019-1480-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Al-Najjar, Rawan M.
Fonseca, Rafael
An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
title An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
title_full An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
title_fullStr An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
title_full_unstemmed An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
title_short An atypical case of Klippel-Trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
title_sort atypical case of klippel-trénaunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451243/
https://www.ncbi.nlm.nih.gov/pubmed/30954069
http://dx.doi.org/10.1186/s12887-019-1480-0
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