Pulmonary arterial stent implantation in an adult with Williams syndrome

Herre J. Reesink, Onno D. F. Henneman, Otto M. van Delden, Jules D. Biervliet, Jaap J. Kloek, Jim A. Reekers, Paul Bresser

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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
Original languageEnglish
Pages (from-to)782-785
JournalCardiovascular and interventional radiology
Volume30
Issue number4
DOIs
Publication statusPublished - 2007

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