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Budd-Chiari syndrome in a 33-year-old woman with hypercoagulable state: A case report
Laleh Abbasi1, Alireza Motamedi2, Ali Kiaee1
1School of Medicine, Tonekabon branch, Islamic Azad University, Tonekabon, Iran.
Insights
Budd-Chiari syndrome (BCS), a rare hepatic venous outflow obstruction, was diagnosed in a woman with protein deficiencies. Early recognition and imaging are crucial for managing this complex condition.
Area of Science:
- Hepatology
- Vascular Medicine
- Thrombosis Research
Background:
- Budd-Chiari syndrome (BCS) results from hepatic venous outflow obstruction.
- It is frequently associated with prothrombotic conditions.
- Understanding these links is vital for patient management.
Observation:
- A 33-year-old woman presented with abdominal pain and ascites.
- Diagnosis of BCS was secondary to deficiencies in protein C, protein S, and antithrombin III.
- Patient had a history of epilepsy, bipolar disorder, and poor medication adherence.
Findings:
- Doppler ultrasound and contrast-enhanced CT confirmed BCS.
- Treatment with anticoagulation and diuretics was initiated.
- Recurrent ascites and behavioral issues complicated management, indicating a poor prognosis.
Implications:
- This case underscores the importance of early BCS recognition.
- Diagnostic imaging is critical for BCS confirmation.
- Evaluating prothrombotic disorders in BCS patients can improve outcomes.
Abstract:
Budd-Chiari syndrome (BCS) is a rare disorder caused by hepatic venous outflow obstruction, often linked to underlying prothrombotic conditions. This case describes a 33-year-old woman who presented with abdominal pain and ascites and was diagnosed with BCS secondary to deficiencies in protein C, protein S, and antithrombin III. She also had a history of epilepsy, bipolar disorder, and poor medication adherence. Imaging studies, including Doppler ultrasound and contrast-enhanced CT, played a crucial role in confirming the diagnosis. Despite treatment with anticoagulation and diuretics, recurrent ascites and behavioral issues complicated management, leading to a poor prognosis. This case highlights the importance of early recognition, imaging in diagnosis, and evaluation of prothrombotic disorders in patients with BCS to improve outcomes.
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