A rare pediatric case: Budd-Chiari Syndrome and upper gastrointestinal bleeding in a 5-year-old boy
Mohamed Ismail Ibrahim, Ahmed Abdi Aw Egge, Omar Ali Elmi, Mohamoud Hashi Abdi, Mohamed Ali Abdilahi, Abdirahman Omer Ali

TL;DR
A rare case of Budd-Chiari Syndrome in a 5-year-old boy highlights challenges in diagnosis and treatment in resource-limited settings.
Contribution
This case report adds to the limited literature on pediatric Budd-Chiari Syndrome and emphasizes the impact of financial barriers on treatment access.
Findings
The case demonstrates the diagnostic difficulty of BCS due to atypical symptoms in children.
Financial constraints hindered access to critical treatment (TIPS), underscoring healthcare disparities.
Multidisciplinary care and early intervention are crucial for managing BCS and preventing complications.
Abstract
Budd-Chiari Syndrome (BCS) is a rare condition characterized by hepatic venous outflow obstruction, often presenting with ascites, hepatomegaly, and abdominal pain. The diagnosis and management of BCS, especially in resource-limited settings, pose significant challenges that can lead to poor patient outcomes. This case report describes a previously healthy individual presenting with progressive abdominal distention, hematemesis, and right upper quadrant pain. The patient had a history of trauma and underwent subsequent percutaneous drainage for ascites. Imaging studies revealed non-opacified hepatic veins, splenomegaly, ascites, and a “nutmeg liver” pattern, confirming the diagnosis of BCS. The patient received blood transfusions, diuretics, and nutritional support. A Transjugular Intrahepatic Portosystemic Shunt (TIPS) procedure was planned but ultimately hindered by financial…
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Taxonomy
TopicsLiver Disease and Transplantation · Abdominal vascular conditions and treatments · Gastrointestinal Bleeding Diagnosis and Treatment
