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Left hepatic lobe agenesis, a rare anatomical condition
Helena Gómez Facundo1, Daniel Rolando Coronado Llanos2, Pilar Lozano3
1Cirugía General y del Aparato Digestivo, Consorci Sanitari Integral, España.
Revista Espanola De Enfermedades Digestivas
|March 8, 2022
Summary
Left hepatic lobe agenesis is a rare congenital disorder. This case report details its diagnosis during an investigation of obstructive jaundice in a male patient.
Area of Science:
- Hepatology
- Congenital Disorders
- Medical Imaging
Background:
- Left hepatic lobe agenesis is an extremely rare congenital condition, with fewer than 40 cases documented since its initial report in 1898.
- Congenital liver anomalies are infrequently encountered, making comprehensive understanding challenging.
Observation:
- The study presents a unique case of a male patient diagnosed with left hepatic lobe agenesis.
- The diagnosis was incidentally made during the etiological investigation of obstructive jaundice.
Findings:
- The case highlights the importance of considering rare congenital anomalies in the differential diagnosis of obstructive jaundice.
- Advanced imaging modalities were crucial in identifying the agenesis of the left hepatic lobe.
Implications:
- This case contributes to the limited literature on left hepatic lobe agenesis, enhancing clinical awareness.
- Understanding such rare conditions is vital for accurate diagnosis and appropriate patient management in hepatobiliary medicine.
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