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1.
Ann Hepatol ; 17(4): 638-644, 2018.
Article in English | MEDLINE | ID: mdl-29893705

ABSTRACT

INTRODUCTION AND AIM: Budd-Chiari syndrome (BCS) is caused by hepatic venous outflow obstruction. This work aims to analyze the pattern of vascular involvement in Egyptian patients with BCS, demonstrates its relation to etiology and shows its impact on clinical presentation. MATERIAL AND METHODS: The current retrospective study was conducted at The Tropical Medicine Department, Ain Shams University on one hundred Egyptian patients with confirmed diagnosis of primary BCS who were presented to the Budd-Chiari Study Group (BCSG) from April 2014 to May 2016 by collecting clinical, laboratory and radiological data from their medical records. RESULTS: Isolated hepatic vein occlusion (HVO) was the most common pattern of vascular involvement (43%), followed by combined HVO and inferior vena cava (IVC) compression by enlarged caudate lobe (32%), then combined HVO and IVC stenosis/webs (21%), and lastly isolated IVC occlusion (4%). Ascites was more significantly encountered in BCS patients with HVO than in those with isolated inferior vena cava (IVC) occlusion and patent HVs (P = 0.005). Abdominal pain was significantly encountered in patients with occluded three major HVs (P = 0.044). Behcet's disease was significantly detected in isolated IVC occlusion. Protein C deficiency was significantly detected in patients with combined HVO and IVC compression. CONCLUSION: Isolated HVs occlusion was the most common pattern of vascular involvement in Egyptian patients with primary BCS. Vascular pattern of involvement affected the clinical presentation and was related to the underlying thrombophilia in those patients.


Subject(s)
Budd-Chiari Syndrome/etiology , Hepatic Veins , Hepatic Veno-Occlusive Disease/etiology , Vena Cava, Inferior , Adolescent , Adult , Budd-Chiari Syndrome/diagnostic imaging , Constriction, Pathologic , Egypt , Female , Hepatic Veins/diagnostic imaging , Hepatic Veno-Occlusive Disease/diagnostic imaging , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Risk Factors , Vena Cava, Inferior/diagnostic imaging , Young Adult
2.
World J Gastroenterol ; 23(4): 629-637, 2017 Jan 28.
Article in English | MEDLINE | ID: mdl-28216969

ABSTRACT

AIM: To compare predictive ability of Budd-Chiari syndrome (BCS) prognostic indices (PIs) for one-year survival and Transjugular intrahepatic portosystemic shunt (TIPS) patency. METHODS: This retrospective study enrolled 194 Egyptian patients with primary BCS who presented to the Budd-Chiari Study Group of Ain Shams University Hospital. Calculation of the available PIs was performed using Child-Pugh and model for end-stage liver disease scores, BCS-specific PIs (Clichy, New Clichy and Rotterdam) for all patients, and BCS-TIPS PI only for patients who underwent TIPS. The overall one-year survival rate and the one-year shunt patency rate for TIPS were reported. RESULTS: The overall one-year survival rate was 69.6%, and the New Clichy PI revealed the best validity for its prediction at a cut-off value of 3.75, with sensitivity and specificity of 78% and 73.3%, respectively [area under receiver operating characteristic curve (AUC) = 0.806]. The one-year survival rate post-TIPS was 89.7%, and the BCS-TIPS score demonstrated validity for its prediction at a cut-off value of 3.92 (sensitivity and specificity were 71.4% and 64.5%, respectively) (AUC = 0.715). Logistic regression analysis revealed that the New Clichy PI (P = 0.030), high serum total bilirubin (P = 0.047) and low albumin (P < 0.001) were independent factors for predicting mortality within one year. The one-year shunt patency rate in TIPS was 80.2%, and none of the PIs exhibited significant validity for its prediction. CONCLUSION: The New Clichy score could independently predict the one-year survival in Egyptian BCS patients.


Subject(s)
Budd-Chiari Syndrome/diagnosis , Portasystemic Shunt, Transjugular Intrahepatic , Adult , Area Under Curve , Egypt , Female , Humans , Male , Prognosis , ROC Curve , Regression Analysis , Reproducibility of Results , Retrospective Studies , Sensitivity and Specificity , Stents , Survival Rate , Treatment Outcome , Young Adult
3.
Liver Int ; 37(3): 415-422, 2017 03.
Article in English | MEDLINE | ID: mdl-27507647

ABSTRACT

BACKGROUND & AIM: Budd-Chiari syndrome (BCS) is caused by hepatic venous outflow obstruction. This work aimed at analyzing characteristics and factors associated with development of hepatocellular carcinoma (HCC) in patients with primary BCS. METHODS: A total of 348 Egyptian BCS patients were included. They were presented to the Budd-Chiari Study Group of Ain Shams University Hospital. BCS was confirmed using abdominal Doppler US. Abdominal magnetic resonance imaging (MRI), MR venography and/or multislice computed tomography (CT) were performed to confirm all diagnoses and to assess vascular anatomy. Hepatic focal lesions detected during the study period (2005-2011) were evaluated using serum alpha foetoprotein (AFP) level, imaging features and histopathological examination. RESULTS: Diagnosis of HCC was confirmed in 15/348 patients (4.3%). Imaging studies showed that 60% had multiple hepatic focal lesions ranging from 2 to 6.3 cm in size. The median level of serum AFP in BCS with HCC was 300 ng/mL vs 11 ng/mL in those without HCC (P<.001). A cut-off level >24.5 ng/mL for serum AFP showed sensitivity 80%, specificity 97.9%, positive predictive value 93.18% and negative predictive value 99.1% for detection of HCC in BCS patients. Male gender, older age, cigarette smoking, serum AFP (>24.5 ng/mL) and shrunken liver by ultrasonography were independent factors associated with HCC development. CONCLUSION: Male gender, older age and cigarette smoking are independent risk factors for development of HCC in BCS. Serum AFP is a good screening test in BCS.


Subject(s)
Budd-Chiari Syndrome/blood , Budd-Chiari Syndrome/complications , Carcinoma, Hepatocellular/pathology , Liver Neoplasms/pathology , Adult , Carcinoma, Hepatocellular/diagnosis , Egypt/epidemiology , Female , Humans , Liver Neoplasms/diagnosis , Logistic Models , Magnetic Resonance Imaging , Male , Multivariate Analysis , Predictive Value of Tests , Retrospective Studies , Risk Factors , Sex Factors , Smoking/adverse effects , Tomography, X-Ray Computed , Ultrasonography, Doppler , Young Adult , alpha-Fetoproteins/analysis
5.
World J Gastroenterol ; 17(42): 4704-10, 2011 Nov 14.
Article in English | MEDLINE | ID: mdl-22180713

ABSTRACT

AIM: To describe the socio-demographic features, etiology, and risk factors for Budd-Chiari syndrome (BCS) in Egyptian patients. METHODS: Ninety-four Egyptian patients with confirmed primary Budd-Chiari syndrome were presented to the Budd-Chiari Study Group (BCSG) and admitted to the Tropical Medicine Department of Ain Shams University Hospital (Cairo, Egypt). Complete clinical evaluation and laboratory investigations, including a thrombophilia workup and full radiological assessment, were performed to determine underlying disease etiologies. RESULTS: BCS was chronic in 79.8% of patients, acute or subacute in 19.1%, and fulminant in 1.1%. Factor V Leiden mutation (FVLM) was the most common etiological cause of disease (53.1%), followed by mutation of the gene encoding methylene tetrahydrofolate reductase (MTHFR) (51.6%). Current or recent hormonal treatment was documented in 15.5% of females, and BCS associated with pregnancy was present in 17.2% of females. Etiology could not be determined in 8.5% of patients. Males had significantly higher rates of MTHFR gene mutation and Behçet's disease, and females had significantly higher rates of secondary antiphospholipid antibody syndrome. A highly significant positive relationship was evident between the presence of Behçet's disease and inferior vena caval occlusion, either alone or combined with occlusion of the hepatic veins (P < 0.0001). CONCLUSION: FVLM is the most common disease etiology and MTHFR the second most common in Egyptian BCS patients. BCS etiology tends to vary with geographic region.


Subject(s)
Budd-Chiari Syndrome/epidemiology , Budd-Chiari Syndrome/genetics , Adult , Budd-Chiari Syndrome/etiology , Budd-Chiari Syndrome/pathology , Egypt/epidemiology , Factor V/genetics , Female , Humans , Male , Methylenetetrahydrofolate Reductase (NADPH2)/genetics , Mutation , Pregnancy , Pregnancy Complications/genetics , Risk Factors , Young Adult
6.
World J Gastroenterol ; 17(7): 906-13, 2011 Feb 21.
Article in English | MEDLINE | ID: mdl-21412499

ABSTRACT

AIM: To evaluate outcome of patients with Budd-Chiari syndrome after balloon angioplasty ± stenting or transjugular intrahepatic portosystemic shunt (TIPS). METHODS: Twenty five patients with Budd-Chiari syndrome admitted to Ain Shams University Hospitals, Tropical Medicine Department were included. Twelve patients (48%) with short segment occlusion were candidates for angioplasty; with stenting in ten cases and without stenting in two. Thirteen patients (52%) had Transjugular Intrahepatic Portosystemic Shunt. Patients were followed up for 12-32 mo. RESULTS: Patency rate in patients who underwent angioplasty ± stenting was 83.3% at one year and at end of follow up. The need of revision was 41.6% with one year survival of 100%, dropped to 91.6% at end of follow up. In patients who had Transjugular Intrahepatic Portosystemic Shunt, patency rate was 92.3% at one year, dropped to 84.6% at end of follow up. The need of revision was 38.4% with one year and end of follow up survival of 100%. Patients with patent shunts showed marked improvement compared to those with occluded shunts. CONCLUSION: Morbidity and mortality following angioplasty ± stenting and TIPS are low with satisfactory outcome. Proper patient selection and management of shunt dysfunction are crucial in improvement.


Subject(s)
Angioplasty, Balloon , Budd-Chiari Syndrome/ethnology , Budd-Chiari Syndrome/therapy , Portasystemic Shunt, Transjugular Intrahepatic , Stents , Adolescent , Adult , Budd-Chiari Syndrome/mortality , Egypt , Female , Follow-Up Studies , Humans , Male , Middle Aged , Prospective Studies , Survival Rate , Treatment Outcome , Young Adult
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