Pulmonary arterial stent implantation in an adult with Williams syndrome

Cardiovasc Intervent Radiol. 2007 Jul-Aug;30(4):782-5. doi: 10.1007/s00270-007-9009-6.

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.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Angiography, Digital Subtraction
  • Angioplasty, Balloon*
  • Chromosome Deletion
  • Chromosomes, Human, Pair 7
  • Diagnosis, Differential
  • Female
  • Humans
  • Hypertension, Pulmonary / diagnostic imaging
  • Hypertension, Pulmonary / genetics
  • Hypertension, Pulmonary / therapy*
  • Image Processing, Computer-Assisted
  • Imaging, Three-Dimensional
  • Pulmonary Artery* / diagnostic imaging
  • Pulmonary Atresia / diagnostic imaging
  • Pulmonary Atresia / genetics
  • Pulmonary Atresia / therapy*
  • Pulmonary Embolism / diagnostic imaging
  • Pulmonary Embolism / therapy
  • Retreatment
  • Stents*
  • Tomography, X-Ray Computed
  • Williams Syndrome / diagnostic imaging
  • Williams Syndrome / genetics
  • Williams Syndrome / therapy*