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Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt

BACKGROUND AND OBJECTIVES: Budd-Chiari syndrome (BCS) is a rare disorder caused by obstruction to hepatic venous outflow. It affects all races, usually during the third or fourth decade of life. Higher prevalence had being evident in developing countries. The aim of the present study was to clarify...

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Autores principales: Abdel Hameed, Muhamad R, Elbeih, Esam Abdel-Moneim Sadek, Abd El-Aziz, Heba Mahmoud, Afifi, Ola Abdel-Haleem, Khalaf, Lamiaa Mohammed Refaat, Ali Abu Rahma, Mohammed Zakaria, Sabry, Abeer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779296/
https://www.ncbi.nlm.nih.gov/pubmed/33408545
http://dx.doi.org/10.2147/JBM.S278678
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author Abdel Hameed, Muhamad R
Elbeih, Esam Abdel-Moneim Sadek
Abd El-Aziz, Heba Mahmoud
Afifi, Ola Abdel-Haleem
Khalaf, Lamiaa Mohammed Refaat
Ali Abu Rahma, Mohammed Zakaria
Sabry, Abeer
author_facet Abdel Hameed, Muhamad R
Elbeih, Esam Abdel-Moneim Sadek
Abd El-Aziz, Heba Mahmoud
Afifi, Ola Abdel-Haleem
Khalaf, Lamiaa Mohammed Refaat
Ali Abu Rahma, Mohammed Zakaria
Sabry, Abeer
author_sort Abdel Hameed, Muhamad R
collection PubMed
description BACKGROUND AND OBJECTIVES: Budd-Chiari syndrome (BCS) is a rare disorder caused by obstruction to hepatic venous outflow. It affects all races, usually during the third or fourth decade of life. Higher prevalence had being evident in developing countries. The aim of the present study was to clarify sociodemographic features, clinical, radiological presentations, and etiology of BCS among Upper Egyptian patients. PATIENTS AND METHODS: This retrospective cohort study enrolled 50 Upper Egyptian Patients with confirmed primary BCS. Liver, coagulation, and thrombophilia workup profiles were performed as anticardiolipin antibodies, lupus anticoagulant, protein C, protein S, and antithrombin III assays. Factor V Leiden and JAK2 mutations were assessed. Full radiological assessment was done. RESULTS: Fifty patients were included. There were 28 males (56%) and 22 females (44%) with mean age (32.5 ± 11.1 years). The etiological factor was not identified in 22% of cases (n=11). Isolated factor C deficiency was found in 26% (n=13) with male predominance 39.3% and protein S deficiency in 10% (n=5). Factor V Leiden mutation was the etiology in 5 patients (10%). Membranous web and antiphospholipid syndrome each were the etiology in 8% (n=4). Behςet’s disease was diagnosed in 4% (n=2). Cases of liver cirrhosis(LC) were 41/50(82%)they were :33/50(66%) LC child class C, 8 /50(16%)  LC child class B, and 0/50 (0%) LC child class A. Abdominal pain was the most common symptom (96%), and ascites was the most common sign (82%). Obstruction of hepatic veins was present in 80%. CONCLUSION: BCS in Upper Egyptian patients was mainly occurred in males in the third and fourth decade of life, mostly with liver cirrhosis. The most common etiology is isolated protein C deficiency followed by Factor V Leiden mutation and isolated protein S deficiency. Hepatic veins obstruction was the most common pattern of vascular involvement.
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spelling pubmed-77792962021-01-05 Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt Abdel Hameed, Muhamad R Elbeih, Esam Abdel-Moneim Sadek Abd El-Aziz, Heba Mahmoud Afifi, Ola Abdel-Haleem Khalaf, Lamiaa Mohammed Refaat Ali Abu Rahma, Mohammed Zakaria Sabry, Abeer J Blood Med Original Research BACKGROUND AND OBJECTIVES: Budd-Chiari syndrome (BCS) is a rare disorder caused by obstruction to hepatic venous outflow. It affects all races, usually during the third or fourth decade of life. Higher prevalence had being evident in developing countries. The aim of the present study was to clarify sociodemographic features, clinical, radiological presentations, and etiology of BCS among Upper Egyptian patients. PATIENTS AND METHODS: This retrospective cohort study enrolled 50 Upper Egyptian Patients with confirmed primary BCS. Liver, coagulation, and thrombophilia workup profiles were performed as anticardiolipin antibodies, lupus anticoagulant, protein C, protein S, and antithrombin III assays. Factor V Leiden and JAK2 mutations were assessed. Full radiological assessment was done. RESULTS: Fifty patients were included. There were 28 males (56%) and 22 females (44%) with mean age (32.5 ± 11.1 years). The etiological factor was not identified in 22% of cases (n=11). Isolated factor C deficiency was found in 26% (n=13) with male predominance 39.3% and protein S deficiency in 10% (n=5). Factor V Leiden mutation was the etiology in 5 patients (10%). Membranous web and antiphospholipid syndrome each were the etiology in 8% (n=4). Behςet’s disease was diagnosed in 4% (n=2). Cases of liver cirrhosis(LC) were 41/50(82%)they were :33/50(66%) LC child class C, 8 /50(16%)  LC child class B, and 0/50 (0%) LC child class A. Abdominal pain was the most common symptom (96%), and ascites was the most common sign (82%). Obstruction of hepatic veins was present in 80%. CONCLUSION: BCS in Upper Egyptian patients was mainly occurred in males in the third and fourth decade of life, mostly with liver cirrhosis. The most common etiology is isolated protein C deficiency followed by Factor V Leiden mutation and isolated protein S deficiency. Hepatic veins obstruction was the most common pattern of vascular involvement. Dove 2020-12-30 /pmc/articles/PMC7779296/ /pubmed/33408545 http://dx.doi.org/10.2147/JBM.S278678 Text en © 2020 Abdel Hameed et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Abdel Hameed, Muhamad R
Elbeih, Esam Abdel-Moneim Sadek
Abd El-Aziz, Heba Mahmoud
Afifi, Ola Abdel-Haleem
Khalaf, Lamiaa Mohammed Refaat
Ali Abu Rahma, Mohammed Zakaria
Sabry, Abeer
Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt
title Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt
title_full Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt
title_fullStr Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt
title_full_unstemmed Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt
title_short Epidemiological Characteristics and Etiology of Budd-Chiari Syndrome in Upper Egypt
title_sort epidemiological characteristics and etiology of budd-chiari syndrome in upper egypt
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779296/
https://www.ncbi.nlm.nih.gov/pubmed/33408545
http://dx.doi.org/10.2147/JBM.S278678
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