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 language | English |
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Pages (from-to) | 782-785 |
Journal | Cardiovascular and interventional radiology |
Volume | 30 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2007 |