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Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome

Klippel–Trenaunay syndrome (KTS) is a rare slow-flow combined vascular malformation characterized by capillary-lymphatic-venous lesions with soft tissue overgrowth of the limbs. We report the case of a 37-year-old female KTS patient with a deep femoral arterial aneurysm. We finally diagnosed that th...

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Detalles Bibliográficos
Autores principales: Ohta, Takashi, Matsubara, Shinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese College of Angiology / The Japanese Society for Vascular Surgery / Japanese Society of Phlebology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758587/
https://www.ncbi.nlm.nih.gov/pubmed/33391551
http://dx.doi.org/10.3400/avd.ra.20-00089
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author Ohta, Takashi
Matsubara, Shinobu
author_facet Ohta, Takashi
Matsubara, Shinobu
author_sort Ohta, Takashi
collection PubMed
description Klippel–Trenaunay syndrome (KTS) is a rare slow-flow combined vascular malformation characterized by capillary-lymphatic-venous lesions with soft tissue overgrowth of the limbs. We report the case of a 37-year-old female KTS patient with a deep femoral arterial aneurysm. We finally diagnosed that the aneurysm had resulted from a fundamental defect in the arterial wall structure. We discuss whether the use of “aneurysm associated with KTS” is accurate and how to better classify this type of capillary-venous lesion in 17 reported KTS patients with arterial aneurysms. In this review, we describe nosological problems of arterial aneurysms associated with KTS.
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spelling pubmed-77585872020-12-31 Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome Ohta, Takashi Matsubara, Shinobu Ann Vasc Dis Review Article Klippel–Trenaunay syndrome (KTS) is a rare slow-flow combined vascular malformation characterized by capillary-lymphatic-venous lesions with soft tissue overgrowth of the limbs. We report the case of a 37-year-old female KTS patient with a deep femoral arterial aneurysm. We finally diagnosed that the aneurysm had resulted from a fundamental defect in the arterial wall structure. We discuss whether the use of “aneurysm associated with KTS” is accurate and how to better classify this type of capillary-venous lesion in 17 reported KTS patients with arterial aneurysms. In this review, we describe nosological problems of arterial aneurysms associated with KTS. Japanese College of Angiology / The Japanese Society for Vascular Surgery / Japanese Society of Phlebology 2020-12-25 /pmc/articles/PMC7758587/ /pubmed/33391551 http://dx.doi.org/10.3400/avd.ra.20-00089 Text en © 2020 The Editorial Committee of Annals of Vascular Diseases. http://creativecommons.org/licenses/by/2.5/ This article is distributed under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided the credit of the original work, a link to the license, and indication of any change are properly given, and the original work is not used for commercial purposes. Remixed or transformed contributions must be distributed under the same license as the original.
spellingShingle Review Article
Ohta, Takashi
Matsubara, Shinobu
Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
title Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
title_full Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
title_fullStr Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
title_full_unstemmed Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
title_short Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
title_sort nosological consideration of arterial aneurysms associated with klippel–trenaunay syndrome
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758587/
https://www.ncbi.nlm.nih.gov/pubmed/33391551
http://dx.doi.org/10.3400/avd.ra.20-00089
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