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Developmental venous anomaly coexisting with arteriovenous malformation: a case report
Mei Li1, JiangBo Ding2, XiTao Zong2
1Department of General Medicine, South Yunnan Central Hospital of Yunnan Province (The First People's Hospital of Honghe Prefecture), Mengzi, China.
Frontiers in Surgery
|April 2, 2025
Summary
A rare case highlights that developmental venous anomalies, often linked with arteriovenous malformations, can be susceptible to blood flow changes, potentially causing complications like aphasia after treatment.
Area of Science:
- Neurovascular Medicine
- Vascular Malformations
- Neurosurgery
Background:
- Developmental venous anomalies (DVAs) are common congenital vascular malformations.
- Arteriovenous malformations (AVMs) are complex tangles of abnormal blood vessels.
- Co-occurrence of DVAs and AVMs is rare but clinically significant.
Observation:
- A 20-year-old male presented with seizures secondary to a left parietal AVM and a left frontal DVA.
- Both lesions shared a common draining vein, despite anatomical separation.
- Post-resection of the AVM, the patient developed progressive aphasia.
Findings:
- Neuroimaging revealed thrombosis in the draining vein of the DVA.
- Aphasia resolved with anticoagulant therapy using low molecular weight heparin.
- This suggests DVAs, despite normal drainage, are sensitive to hemodynamic shifts.
Implications:
- This case supports the understanding of DVA venous drainage patterns.
- It highlights the potential risk of thrombosis and neurological deficits in DVAs.
- Management of co-existing DVAs and AVMs requires careful consideration of venous hemodynamics.
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