Budd-Chiari syndrome in a 33-year-old woman with hypercoagulable state: A case report

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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Publication Details

Journal
Radiology Case Reports
Published
2025-04-12
DOI
https://doi.org/10.1016/j.radcr.2025.03.023
Primary Topic
Tuberous Sclerosis Complex Research
Type
article
Field-Weighted Citation Impact
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article

Budd-Chiari syndrome in a 33-year-old woman with hypercoagulable state: A case report

Alireza Motamedi, Fatemeh Abbası, Ali Kiaee, Laleh Abbasi et al.
Radiology Case Reports
Tuberous Sclerosis Complex Research
article

Budd-Chiari syndrome in a 33-year-old woman with hypercoagulable state: A case report

Alireza Motamedi, Fatemeh Abbası, Ali Kiaee, Laleh Abbasi, Ommolbanin Younesian, Nazgol Khodaie
article en

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.

Radiology Case ReportsVol. 20(7)
Tabriz University of Medical Sciences (IR), Islamic Azad University Tonekabon (IR)
Openalex Percentile: Top 91%
Tuberous Sclerosis Complex Research
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