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Published on: August 8, 2022
Diffuse angiodysplasia of the upper gastrointestinal tract in a patient with hypertrophic obstructive cardiomyopathy
H Fujita1, J Tomiyama, Y Chuganji
1Department of Internal Medicine, Tokyo Metropolitan Bokutou General Hospital.
Insights
A rare case of severe anemia caused by gastrointestinal angiodysplasia in a patient with hypertrophic obstructive cardiomyopathy highlights a challenging diagnostic scenario.
Area of Science:
- Cardiology
- Gastroenterology
- Hematology
Background:
- Hypertrophic obstructive cardiomyopathy (HOCM) is a complex cardiac condition.
- Gastrointestinal bleeding can lead to severe anemia of unknown origin.
- Angiodysplasia is a vascular malformation that can cause bleeding.
Observation:
- A 64-year-old woman with HOCM presented with severe anemia and recurrent upper gastrointestinal bleeding.
- Extensive investigations including bone marrow examination and endoscopy were inconclusive.
- A bleeding site identified during duodenoscopy was diagnosed as angiodysplasia.
Findings:
- Gastrointestinal angiodysplasia was identified as the source of bleeding and the cause of anemia.
- This case highlights a rare association between gastrointestinal angiodysplasia and subvalvular aortic obstruction.
Implications:
- This case underscores the importance of considering gastrointestinal angiodysplasia in patients with unexplained anemia and bleeding, especially those with cardiac conditions.
- Further research into the link between HOCM and gastrointestinal angiodysplasia may improve diagnostic and treatment strategies.
- Early diagnosis and management of gastrointestinal angiodysplasia can prevent severe anemia and complications.
Abstract:
A 64-year-old woman with a known history of hypertrophic obstructive cardiomyopathy presented with severe anemia of unknown origin. She had also suffered from repeated episodes of upper gastrointestinal bleeding for the previous 3 years. Despite bone marrow examination and panendoscopic and angiographic studies, the origin of anemia remained undefined until a small bleeding site was found during a duodenoscopic examination. The lesion proved to be angiodysplasia. This case report is interesting in that angiodysplasia elicited gastrointestinal bleeding and was the cause of anemia. In the international literature, there are very few reported cases of bleeding from gastrointestinal angiodysplasia in association with subvalvular aortic obstruction.
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