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1 ut was present in 62.5% of the patients with portal vein thrombosis.
2 There was no incidence of hepatic artery or portal vein thrombosis.
3 Three (2.9%) grafts were lost due to portal vein thrombosis.
4 y independent risk factor for pre-transplant portal vein thrombosis.
5 es because of unexpected acute rejection and portal vein thrombosis.
6 ing for age, sex, treatment, tumor size, and portal vein thrombosis.
7 patient required retransplantation, owing to portal vein thrombosis.
8 ies, 8 required surgical shunts for complete portal vein thrombosis.
9 hic scan showed superior mesenteric vein and portal vein thrombosis.
10 t entry criteria, and 2 were excluded due to portal vein thrombosis.
11 4), acute chest syndrome (5), pneumonia (2), portal vein thrombosis (1), priapism (1), hemolytic urem
12 were mainly rejected for comorbidity (19%), portal vein thrombosis (16%), previous surgery (9%), obe
13 ently in OPV than in cirrhosis: extrahepatic portal vein thrombosis (18 [43%] of 42 vs five [12%] of
14 .4%; 20-year survival, 12.5%). patients with portal vein thrombosis and biliary cirrhosis demonstrate
15 wo (16.3%) patients developed pre-transplant portal vein thrombosis and its presence had no impact in
16 tic thrombosis, and radiologic management of portal vein thrombosis and stenosis has decreased operat
18 C, 56% had more than 1 tumor nodule, 24% had portal vein thrombosis, and 29% did not receive any canc
19 ism, disseminated intravascular coagulation, portal vein thrombosis, and arterial thromboembolism.
21 analysis Child-Pugh score, presence of HCC, portal vein thrombosis, and lack of secondary prophylaxi
25 tis/cholecystitis, pancreatitis, hemorrhage, portal vein thrombosis, bowel wall perforation, or dehyd
26 f orthotopic liver transplantation, in which portal vein thrombosis developed in the immediate postop
28 s of the liver in children with extrahepatic portal vein thrombosis (EHPVT), with surgical outcome af
30 last decade a large number of patients with portal vein thrombosis have undergone successful liver t
31 We aimed to characterize the pre-transplant portal vein thrombosis in a cohort of liver transplant r
32 ascular stent placement for the treatment of portal vein thrombosis in liver transplant recipients.
33 nt placement were successfully used to treat portal vein thrombosis in patients with recent liver tra
36 patients with Budd-Chiari syndrome and with portal vein thrombosis, Kiladjian et al observed that JA
37 n associated with hepatic artery (n = 15) or portal vein thrombosis (n = 14).Mean surgical time was 1
38 pared with non-BCS liver recipients), one of portal vein thrombosis (nonsignificant [NS]), and one of
39 t survival for patients who have experienced portal vein thrombosis or stenosis is 61% and 67%, respe
41 ardial infarct, perioperative hemorrhage, or portal vein thrombosis--or death occurred as a result of
42 001), MELD score greater than 10 (P = .001), portal vein thrombosis (P = .0001), and tumor diameter g
43 nt differences in hepatic artery thrombosis, portal vein thrombosis, primary nonfunction, and biliary
44 s possible even in the presence of recipient portal vein thrombosis, provided that hepatopetal portal
45 logy Group (ECOG), presence of cirrhosis and portal vein thrombosis (PVT) (none, branch, and main).
47 patients of liver cirrhosis associated with portal vein thrombosis (PVT) can be effectively treated
50 low-molecular-weight heparin, in preventing portal vein thrombosis (PVT) in patients with advanced c
53 ate and survival of hepatocellular carcinoma portal vein thrombosis (PVT) patients treated with (90)Y
54 Patients with Child-Pugh B disease who had portal vein thrombosis (PVT) survived 5.6 months (95% co
55 ed-stage hepatocellular carcinoma (HCC) with portal vein thrombosis (PVT) treated with (90)Y radioemb
56 onths with no significant difference between portal vein thrombosis (PVT) versus no PVT (7 versus 13
58 tients with chronic noncirrhotic, nontumoral portal vein thrombosis (PVT), the usually recommended st
59 ocellular carcinoma (HCC), including 16 with portal vein thrombosis (PVT), were treated with (90)Y-lo
63 atocellular carcinoma (HCC) with and without portal vein thrombosis underwent radioembolization with
64 ease, cytomegalovirus infection and disease, portal vein thrombosis, UNOS status, Childs-Pugh score,
68 60.1 years; range, 32-75 years) with HCC and portal vein thrombosis who were examined with both contr
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