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Published on: May 21, 2017
Persistent Gastrointestinal Bleeding after Aortic Valve Replacement in Heyde's Syndrome
Alexandr Ceasovschih1,2, Raluca-Elena Alexa2, Victorița Șorodoc1,2
1Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Heyde's syndrome, linked to aortic stenosis and intestinal angiodysplasias, involves acquired von Willebrand disease. This case highlights successful management of gastrointestinal bleeding and anemia in an elderly patient with these conditions.
Area of Science:
- Gastroenterology
- Hematology
- Cardiology
Background:
- Heyde's syndrome (HS) links aortic stenosis and intestinal angiodysplasias.
- Acquired von Willebrand disease is key in HS pathophysiology, increasing bleeding risk.
- Von Willebrand factor deficiency exacerbates bleeding and anemia in HS patients.
Purpose of the Study:
- To present a case of Heyde's syndrome with von Willebrand deficiency.
- To illustrate the management of lower gastrointestinal bleeding in this context.
- To demonstrate the efficacy of treating angiodysplastic lesions.
Main Methods:
- Case report of an 86-year-old female patient.
- Diagnosis of HS and von Willebrand deficiency.
- Colonoscopy to identify colonic angiodysplasias.
- Argon plasma coagulation for angiodysplastic lesions.
Main Results:
- Patient presented with anemia, elevated INR and aPTT.
- Lower gastrointestinal bleeding occurred during hospitalization.
- Successful treatment of angiodysplastic lesions led to clinical improvement.
- Anemia resolved following intervention.
Conclusions:
- Argon plasma coagulation is effective for managing gastrointestinal bleeding from angiodysplasias in HS.
- Timely intervention can reverse anemia and improve outcomes in HS patients.
- This case underscores the importance of recognizing and treating HS-related complications.
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