A rare encounter with two cases of Budd‑Chiari syndrome in the Emergency Department: A case report
Budd-Chiari syndrome (BCS) is a rare disorder clinically characterized by abdominal pain, hepatomegaly and ascites. The condition is often related to thrombosis of the hepatic veins or the terminal portion of the inferior vena cava. A myeloproliferative disorder is the most identified underlying pro...
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Published in | Experimental and therapeutic medicine Vol. 24; no. 6 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Athens
Spandidos Publications
01.12.2022
Spandidos Publications UK Ltd D.A. Spandidos |
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Abstract | Budd-Chiari syndrome (BCS) is a rare disorder clinically characterized by abdominal pain, hepatomegaly and ascites. The condition is often related to thrombosis of the hepatic veins or the terminal portion of the inferior vena cava. A myeloproliferative disorder is the most identified underlying prothrombotic risk factor, although almost one-half of affected patients are now recognized as having multiple underlying prothrombotic risk factors. Doppler ultrasound may be enough to confirm the diagnosis of BCS; however, computed tomography or magnetic resonance imaging is often employed. Anticoagulant therapy is the cornerstone of BCS treatment, but most patients also need additional treatment strategies. Most patients with BCS are now treated by endovascular intervention, which has improved survival rate in those afflicted by this disease. The long-term course of the disease can be complicated by progression or recurrence of the underlying myeloproliferative disorder. The present study reports the cases of two patients with BCS with the aim of alerting healthcare workers in Emergency Departments of this less common diagnosis in patients presenting with frequent complaints of abdominal pain. |
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AbstractList | Budd-Chiari syndrome (BCS) is a rare disorder clinically characterized by abdominal pain, hepatomegaly and ascites. The condition is often related to thrombosis of the hepatic veins or the terminal portion of the inferior vena cava. A myeloproliferative disorder is the most identified underlying prothrombotic risk factor, although almost one-half of affected patients are now recognized as having multiple underlying prothrombotic risk factors. Doppler ultrasound may be enough to confirm the diagnosis of BCS; however, computed tomography or magnetic resonance imaging is often employed. Anticoagulant therapy is the cornerstone of BCS treatment, but most patients also need additional treatment strategies. Most patients with BCS are now treated by endovascular intervention, which has improved survival rate in those afflicted by this disease. The long-term course of the disease can be complicated by progression or recurrence of the underlying myeloproliferative disorder. The present study reports the cases of two patients with BCS with the aim of alerting healthcare workers in Emergency Departments of this less common diagnosis in patients presenting with frequent complaints of abdominal pain. Key words: Budd-Chiari syndrome, neoplastic disease, hepatomegaly, hepatic failure, thrombosis, endovascular intervention Budd-Chiari syndrome (BCS) is a rare disorder clinically characterized by abdominal pain, hepatomegaly and ascites. The condition is often related to thrombosis of the hepatic veins or the terminal portion of the inferior vena cava. A myeloproliferative disorder is the most identified underlying prothrombotic risk factor, although almost one-half of affected patients are now recognized as having multiple underlying prothrombotic risk factors. Doppler ultrasound may be enough to confirm the diagnosis of BCS; however, computed tomography or magnetic resonance imaging is often employed. Anticoagulant therapy is the cornerstone of BCS treatment, but most patients also need additional treatment strategies. Most patients with BCS are now treated by endovascular intervention, which has improved survival rate in those afflicted by this disease. The long-term course of the disease can be complicated by progression or recurrence of the underlying myeloproliferative disorder. The present study reports the cases of two patients with BCS with the aim of alerting healthcare workers in Emergency Departments of this less common diagnosis in patients presenting with frequent complaints of abdominal pain. |
ArticleNumber | 730 |
Audience | Academic |
Author | Chiriac, Sorin Dan Mederle, Ovidiu Alexandru Stanciugelu, Alexandra Petrica, Alina Iurciuc, Mircea Boruga, madalina Veronica Balica, Nicolae |
AuthorAffiliation | 3 Department of Emergency, ‘Pius Brînzeu’ Emergency Clinical County Hospital, 300736 Timisoara, Romania 5 Department of Ophthalmology, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania 4 Department of Cardiology, Faculty of Medicine, Multidisciplinary Center for Research, Evaluation, Diagnosis and Therapies in Oral Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania 7 Department of Surgery, Faculty of Medicine, Multidisciplinary Center for Research, Evaluation, Diagnosis and Therapies in Oral Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania 2 Department of Emergency, Emergency Clinical Municipal Hospital, 300079 Timisoara, Romania 6 Department of Ear, Nose and Throat, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania 1 Department of Surgery, Faculty of Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania |
AuthorAffiliation_xml | – name: 4 Department of Cardiology, Faculty of Medicine, Multidisciplinary Center for Research, Evaluation, Diagnosis and Therapies in Oral Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania – name: 6 Department of Ear, Nose and Throat, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania – name: 7 Department of Surgery, Faculty of Medicine, Multidisciplinary Center for Research, Evaluation, Diagnosis and Therapies in Oral Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania – name: 3 Department of Emergency, ‘Pius Brînzeu’ Emergency Clinical County Hospital, 300736 Timisoara, Romania – name: 2 Department of Emergency, Emergency Clinical Municipal Hospital, 300079 Timisoara, Romania – name: 5 Department of Ophthalmology, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania – name: 1 Department of Surgery, Faculty of Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania |
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Copyright | COPYRIGHT 2022 Spandidos Publications Copyright Spandidos Publications UK Ltd. 2022 Copyright: © Stanciugelu et al. 2020 |
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Notes | Dr Mircea Iurciuc, Department of Cardiology, Faculty of Medicine, Multidisciplinary Center for Research, Evaluation, Diagnosis and Therapies in Oral Medicine, ‘Victor Babes’ University of Medicine and Pharmacy, Piata Eftimie Murgu 2, 300041 Timisoara, Romania iurciuc.mircea@umft.ro Contributed equally |
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Snippet | Budd-Chiari syndrome (BCS) is a rare disorder clinically characterized by abdominal pain, hepatomegaly and ascites. The condition is often related to... |
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SubjectTerms | Abdomen Anticoagulants Ascites Care and treatment Case Report Case reports Case studies Diagnosis Edema Emergency medical care Hepatic vein thrombosis Hypertension Liver Medical imaging Medical prognosis Mutation Pain Patients Thrombosis Ultrasonic imaging Veins & arteries |
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Title | A rare encounter with two cases of Budd‑Chiari syndrome in the Emergency Department: A case report |
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