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Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation

Klippel-Trénaunay syndrome (KTS) is a rare vascular congenital anomaly affecting less than 200,000 people in the United States. Vascular malformations associated with KTS tend to affect slow flow systems: venous, capillary, and lymphatic systems. The nature of the syndrome leads to a higher risk for...

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Autores principales: Sadiq, Mahniya F., Shuaib, Waqas, Tiwana, Muhammad H., Johnson, Jamlik-Omari, Khosa, Faisal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932826/
https://www.ncbi.nlm.nih.gov/pubmed/24653849
http://dx.doi.org/10.1155/2014/202160
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author Sadiq, Mahniya F.
Shuaib, Waqas
Tiwana, Muhammad H.
Johnson, Jamlik-Omari
Khosa, Faisal
author_facet Sadiq, Mahniya F.
Shuaib, Waqas
Tiwana, Muhammad H.
Johnson, Jamlik-Omari
Khosa, Faisal
author_sort Sadiq, Mahniya F.
collection PubMed
description Klippel-Trénaunay syndrome (KTS) is a rare vascular congenital anomaly affecting less than 200,000 people in the United States. Vascular malformations associated with KTS tend to affect slow flow systems: venous, capillary, and lymphatic systems. The nature of the syndrome leads to a higher risk for the development of arteriovenous malformations. Our case presentation describes a patient with KTS and an associated rare presentation of intraventricular arteriovenous malformation (AVM).
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spelling pubmed-39328262014-03-20 Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation Sadiq, Mahniya F. Shuaib, Waqas Tiwana, Muhammad H. Johnson, Jamlik-Omari Khosa, Faisal Case Rep Radiol Case Report Klippel-Trénaunay syndrome (KTS) is a rare vascular congenital anomaly affecting less than 200,000 people in the United States. Vascular malformations associated with KTS tend to affect slow flow systems: venous, capillary, and lymphatic systems. The nature of the syndrome leads to a higher risk for the development of arteriovenous malformations. Our case presentation describes a patient with KTS and an associated rare presentation of intraventricular arteriovenous malformation (AVM). Hindawi Publishing Corporation 2014 2014-02-06 /pmc/articles/PMC3932826/ /pubmed/24653849 http://dx.doi.org/10.1155/2014/202160 Text en Copyright © 2014 Mahniya F. Sadiq et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sadiq, Mahniya F.
Shuaib, Waqas
Tiwana, Muhammad H.
Johnson, Jamlik-Omari
Khosa, Faisal
Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
title Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
title_full Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
title_fullStr Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
title_full_unstemmed Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
title_short Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
title_sort klippel-trénaunay syndrome with intracranial arteriovenous malformation: a rare presentation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932826/
https://www.ncbi.nlm.nih.gov/pubmed/24653849
http://dx.doi.org/10.1155/2014/202160
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