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Arterial thrombosis leading to intestinal infarction in a patient with Behçet's disease associated with protein C

Y Bayraktar1, A R Soylu, F Balkanci

  • 1Department of Gastroenterology, Hacettepe University, School of Medicine, Ankara, Turkey.

Insights

Behçet

Area of Science:

  • Vascular Medicine
  • Gastroenterology
  • Rheumatology

Background:

  • Behçet's disease is a rare multisystem inflammatory disorder.
  • It can manifest with vascular complications, including arterial and venous thrombosis.
  • Intestinal infarction is a severe, though uncommon, manifestation.

Observation:

  • A 41-year-old male with a 15-year history of Behçet's disease presented with severe abdominal pain and bloody diarrhea.
  • He had a prior diagnosis of superior mesenteric artery thrombosis leading to intestinal infarction.
  • Recurrent symptoms led to the discovery of an infrarenal abdominal aorta thrombus.

Findings:

  • This case highlights Behçet's disease complicated by recurrent mesenteric artery thrombosis and abdominal aorta thrombosis.
  • Protein C deficiency was identified as a potential secondary factor contributing to the thrombotic events.
  • This represents the first reported instance of combined mesenteric artery and abdominal aorta thrombosis associated with Behçet's disease and protein C deficiency.

Implications:

  • This case underscores the critical need for vigilant monitoring of vascular complications in Behçet's disease patients.
  • It suggests that coexisting thrombophilias, such as protein C deficiency, may increase the risk of severe vascular events.
  • Further research into the interplay between Behçet's disease, vasculitis, and thrombophilia is warranted.

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