Pulmonary arterial stent implantation in an adult with Williams syndrome.

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.

authors

Reesink HJ,Henneman OD,van Delden OM,Biervliet JD,Kloek JJ,Reekers JA,Bresser P

doi

10.1007/s00270-007-9009-6

subject

Has Abstract

pub_date

2007-07-01 00:00:00

pages

782-5

issue

4

eissn

0174-1551

issn

1432-086X

journal_volume

30

pub_type

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