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Abernethy malformation: A comprehensive review
Parveen Kumar1, Mona Bhatia1, Amit Garg1
1Department of Radiodiagnosis and Imaging, Fortis Escort Heart Institute, New Delhi, India.
Abernethy malformation is a rare vascular anomaly where blood bypasses the liver. Treatment depends on the type, ranging from medical management to liver transplantation or shunt occlusion.
Area of Science:
- Vascular Surgery
- Pediatric Surgery
- Medical Imaging
Background:
- Abernethy malformation is a rare congenital portosystemic shunt.
- It involves blood from the portal vein bypassing the liver into systemic circulation.
- Associated anomalies and complications necessitate a thorough understanding.
Purpose of the Study:
- To provide a comprehensive overview of Abernethy malformation.
- To highlight the importance of imaging in diagnosis and management.
- To differentiate Abernethy malformation from other portosystemic shunts.
Main Methods:
- Review of anatomical and embryological principles.
- Discussion of imaging modalities like CT and MR angiography.
- Analysis of diagnostic criteria and differential diagnoses.
Main Results:
- Categorization into Type I (complete shunt) and Type II (partial shunt).
- Association with congenital anomalies and acquired complications.
- Imaging findings crucial for shunt anatomy and anomaly evaluation.
Conclusions:
- Accurate diagnosis requires understanding anatomy, embryology, and imaging.
- Management strategies vary based on malformation type and patient symptoms.
- Type I typically requires liver transplantation; Type II may be treated with shunt occlusion.
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