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Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation
Klippel–Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity. Port wine stain is the most common vascular malformation associated with this syndrome. Various other rare vascular malfor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367591/ https://www.ncbi.nlm.nih.gov/pubmed/32695703 http://dx.doi.org/10.4103/idoj.IDOJ_220_19 |
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author | Supekar, Bhagyashree B. Chopkar, Apoorva D. Wankhade, Vaishali H. Singh, Rajesh Pratap Bhat, Dharitri Mukund Suresh, Parvathy |
author_facet | Supekar, Bhagyashree B. Chopkar, Apoorva D. Wankhade, Vaishali H. Singh, Rajesh Pratap Bhat, Dharitri Mukund Suresh, Parvathy |
author_sort | Supekar, Bhagyashree B. |
collection | PubMed |
description | Klippel–Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity. Port wine stain is the most common vascular malformation associated with this syndrome. Various other rare vascular malformations described are angiokeratomas, angiokeratoma circumscriptum naeviformae, angiodermatitis, etc. This is the first instance, to the best of our knowledge, describing the capillary, venous, and lymphatic malformations in a same case of KTS. |
format | Online Article Text |
id | pubmed-7367591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-73675912020-07-20 Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation Supekar, Bhagyashree B. Chopkar, Apoorva D. Wankhade, Vaishali H. Singh, Rajesh Pratap Bhat, Dharitri Mukund Suresh, Parvathy Indian Dermatol Online J Case Report Klippel–Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity. Port wine stain is the most common vascular malformation associated with this syndrome. Various other rare vascular malformations described are angiokeratomas, angiokeratoma circumscriptum naeviformae, angiodermatitis, etc. This is the first instance, to the best of our knowledge, describing the capillary, venous, and lymphatic malformations in a same case of KTS. Wolters Kluwer - Medknow 2020-05-10 /pmc/articles/PMC7367591/ /pubmed/32695703 http://dx.doi.org/10.4103/idoj.IDOJ_220_19 Text en Copyright: © 2020 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Supekar, Bhagyashree B. Chopkar, Apoorva D. Wankhade, Vaishali H. Singh, Rajesh Pratap Bhat, Dharitri Mukund Suresh, Parvathy Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation |
title | Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation |
title_full | Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation |
title_fullStr | Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation |
title_full_unstemmed | Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation |
title_short | Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation |
title_sort | klippel–trenaunay syndrome with arterio-veno-lymphatic malformation: a rare presentation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367591/ https://www.ncbi.nlm.nih.gov/pubmed/32695703 http://dx.doi.org/10.4103/idoj.IDOJ_220_19 |
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