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HYPOGENESIS OF RIGHT LOBE OF LIVER ACCOMPANIED BY PORTAL HYPERTENSION AND ESOPHAGOGASTRIC VARICEAL BLEEDING; A RARE
M Gurgenidze1, N Lomidze1, K Chelidze1
1Tbilisi State Medical University the First University Clinic, Department of Surgery; Department of Internal Medicine; Department of Radiology, Tbilisi, Georgia.
Congenital hypogenesis of the right liver lobe is a rare condition. This case highlights a patient presenting with upper gastrointestinal bleeding due to esophageal and gastric varices, successfully managed.
Area of Science:
- Hepatology
- Gastroenterology
- Radiology
Background:
- Hypo-agenesis of the right liver lobe is an extremely rare congenital condition.
- It is defined as the partial or complete absence of the right liver lobe without prior disease or surgery.
Observation:
- A 32-year-old female presented with upper gastrointestinal bleeding, nausea, vomiting, and melena.
- Esophagogastroduodenoscopy revealed severe esophageal and gastric varices with active bleeding.
- Computed tomography with angiography identified congenital hypogenesis of the right liver lobe with colonic interposition.
Findings:
- The patient was diagnosed with congenital hypogenesis of the right liver lobe, portal hypertension, and bleeding varices.
- Bleeding was temporarily controlled with a Sengstaken-Blakemore tube.
- The diagnosis included atrophy-hypertrophy complex, hypersplenism, and post-hemorrhagic anemia.
Implications:
- This case underscores the importance of considering rare congenital liver anomalies in patients with unexplained gastrointestinal bleeding.
- Prompt diagnosis and management are crucial for patient outcomes.
- Long-term follow-up is essential to monitor for recurrent bleeding and other complications.
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