Treatment experience of thoracic aortic aneurysm recurrence after multiple surgeries for Marfan syndrome: A case report

Medicine (Baltimore). 2019 Oct;98(40):e17391. doi: 10.1097/MD.0000000000017391.

Abstract

Rationale: Marfan syndrome (MFS), an autosomal dominant hereditary disease, often results in structural and functional abnormalities of the aortic wall. Because of residual aortic aneurysm or aortic dissection, patients with MFS usually need repeat operations after the first operation.

Patient concerns: A patient diagnosed with MFS who had undergone 2 surgeries because of abdominal aortic dissection aneurysm and Stanford A type aortic dissection at different times.

Diagnoses: MFS.

Interventions: Due to aneurysmal dilatation of the residual descending aorta, we performed the third surgery for him through using 2 artificial stent grafts to fix and package the area of the remaining vessel in our hospital.

Outcomes: The result was good, and the patient was discharged successfully.

Lessons: Using artificial material to repair and wrap the area of the residual vessel during the first surgery can provide an anchor area for future endovascular stent implantation and also offer a possibility for stent implantation in patients with MFS.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Aortic Aneurysm, Thoracic / complications*
  • Aortic Aneurysm, Thoracic / surgery*
  • Aortic Dissection / surgery
  • Blood Vessel Prosthesis Implantation / methods*
  • Blood Vessel Prosthesis*
  • Humans
  • Male
  • Marfan Syndrome / complications*