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CardioVascular and Interventional Radiology

, Volume 30, Issue 4, pp 782–785

First Online: 03 April 2007

Abstract

We report a 38-year-old patient who presented with pulmonary hypertension and right ventricular dysfunction due to pulmonary artery stenoses as a manifestation of Williams syndrome, mimicking chronic thromboembolic pulmonary hypertension. The patient was treated with balloon angioplasty and stent implantation. Short-term follow-up showed a good clinical result with excellent patency of the stents but early restenosis of the segments in which only balloon angioplasty was performed. These stenoses were subsequently also treated successfully by stent implantation. Stent patency was observed 3 years after the first procedure.

KeywordsBalloon angioplasty Pulmonary artery stenosis Pulmonary hypertension Stent implantation Williams syndrome  Download fulltext PDF



Autor: Herre J. Reesink - Onno D. F. Henneman - Otto M. van Delden - Jules D. Biervliet - Jaap J. Kloek - Jim A. Reekers -

Fuente: https://link.springer.com/



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