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Phlebectasia of Internal Jugular Vein

Internal jugular phlebectasia (IJP) is a rare disease in which there is a fusiform dilatation of internal jugular vein, usually presenting as a neck mass in children. Accurate diagnosis from careful history, physical examination, and radiological study can be made. We report a 12-year-old boy with h...

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Autores principales: Bindal, Satish K., Vasisth, Gaurav O. P., Chibber, Puneet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673350/
https://www.ncbi.nlm.nih.gov/pubmed/23741586
http://dx.doi.org/10.4103/2006-8808.110266
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author Bindal, Satish K.
Vasisth, Gaurav O. P.
Chibber, Puneet
author_facet Bindal, Satish K.
Vasisth, Gaurav O. P.
Chibber, Puneet
author_sort Bindal, Satish K.
collection PubMed
description Internal jugular phlebectasia (IJP) is a rare disease in which there is a fusiform dilatation of internal jugular vein, usually presenting as a neck mass in children. Accurate diagnosis from careful history, physical examination, and radiological study can be made. We report a 12-year-old boy with history of swelling appearing on the right side of the neck only on straining, coughing, or during a Valsalva maneuver. Diagnosis of right IJP was made. Exploration and wrapping the dilated segment in an 8-mm-diameter polytetrafluoroethylene tube graft was done. Because of its rarity, this entity is frequently ignored or misdiagnosed. This case report intends to stress the importance of keeping IJP as differential diagnosis while dealing with such a swelling to avoid invasive investigations and inappropriate treatment.
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spelling pubmed-36733502013-06-05 Phlebectasia of Internal Jugular Vein Bindal, Satish K. Vasisth, Gaurav O. P. Chibber, Puneet J Surg Tech Case Rep Case Report Internal jugular phlebectasia (IJP) is a rare disease in which there is a fusiform dilatation of internal jugular vein, usually presenting as a neck mass in children. Accurate diagnosis from careful history, physical examination, and radiological study can be made. We report a 12-year-old boy with history of swelling appearing on the right side of the neck only on straining, coughing, or during a Valsalva maneuver. Diagnosis of right IJP was made. Exploration and wrapping the dilated segment in an 8-mm-diameter polytetrafluoroethylene tube graft was done. Because of its rarity, this entity is frequently ignored or misdiagnosed. This case report intends to stress the importance of keeping IJP as differential diagnosis while dealing with such a swelling to avoid invasive investigations and inappropriate treatment. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3673350/ /pubmed/23741586 http://dx.doi.org/10.4103/2006-8808.110266 Text en Copyright: © Journal of Surgical Technique and Case Report http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Bindal, Satish K.
Vasisth, Gaurav O. P.
Chibber, Puneet
Phlebectasia of Internal Jugular Vein
title Phlebectasia of Internal Jugular Vein
title_full Phlebectasia of Internal Jugular Vein
title_fullStr Phlebectasia of Internal Jugular Vein
title_full_unstemmed Phlebectasia of Internal Jugular Vein
title_short Phlebectasia of Internal Jugular Vein
title_sort phlebectasia of internal jugular vein
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673350/
https://www.ncbi.nlm.nih.gov/pubmed/23741586
http://dx.doi.org/10.4103/2006-8808.110266
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