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  • 1
    ISSN: 1436-0691
    Keywords: Key words: cholangiocellular carcinoma ; hepatolithiasis ; hepatic resection ; common bi1e duct exploration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract: We report our experience of the surgical treatment of intrahepatic cholangiocarcinoma (ICC) in Taiwanese patients. A tota1 of 162 patients with histologically proven ICC were treated of whom 106 (65.4%) had associated hepatolithiasis. Patients with hepatolithiasis were in earlier stages than those without hepatolithiasis. Two-thirds of the patients with hepatolithiasis presented with acute cholangitis, and two-thirds of those without hepatolithiasis presented with hepatomegaly. The rate of hepatic resection was 29.6% (48 of 162), and these rates were 31.1% and 26.8% for the patients with and without hepatolithiasis, respectively. Ninety-three percent of the patients with hepatolithiasis underwent common bile duct exploration, compared with 18% of those without hepatolithiasis. The surgical mortality rates were 3.7% (6/162), for all patients, and 3.8% and 3.6% for patients with and without hepatolithiasis, respectively. The morbidity rate was much higher in the patients with hepatolithiasis (37.7% vs 16.1%). The 1-, 3-, and 5-year survival rates were 35.5%, 20.5%, and 16.5% in the patients with hepatolithiasis and 27.2%, 8.8%, and 7.8% in those without hepatolithiasis. Concomitant hepatolithiasis prevented precise diagnosis preoperatively and precipitated biliary sepsis, which affected resectability and increased postoperative morbidity. Hepatolithiasis per se did not influence long-term survival.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-2568
    Keywords: HEPATOCELLULAR CARCINOMA ; HEPATOLITHIASIS ; CHOLANGIOCARCINOMA ; α-FETOPROTEIN ; CARCINOEMBRYONIC ANTIGEN
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Nineteen patients with hepatocellular carcinomaassociated with hepatolithiasis were retrospectivelyanalyzed. Eleven of the 19 patients presented withhepatolithiasis-related biliary infection. Diagnosis was erroneously assumed to be hepatolithiasisalone, liver abscess, or cholangiocarcinoma in five of11 patients before surgery was attempted. Middle-age,male sex, liver cirrhosis, hepatitis B or C infection, abnormal α-fetoprotein, and negativecarcinoembryonic antigen raised the suspicion ofassociated hepatocellular carcinoma rather thancholangiocarcinoma in patients with hepatolithiasis.Antibiotics and nonoperative methods to resolve biliaryinfection first, followed by hepatectomy, in selectedcases, to eradicate hepatocellular carcinoma andhepatolithiasis simultaneously provides the best chance for long-term survival. Otherwise, patientsoften died of hepatolithiasis-related biliary sepsisrather than hepatocellular carcinoma per se in the longrun.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-2568
    Keywords: PANCREATITIS ; HEPATOCELLULAR CARCINOMA ; JAUNDICE ; CHOLANGIOGRAPHY
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 45 (2000), S. 312-316 
    ISSN: 1573-2568
    Keywords: hepatolithiasis ; peripheral cholangiocarcinoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The association of hepatolithiasis (HL) and peripheral cholangiocarcinoma (PCC) has been well recognized. However, information concerning the impact of hepatolithiasis on patients with peripheral cholangiocarcinoma is sparse and therefore difficult to assess. A total of 162 consecutive patients with histologically proven peripheral cholangiocarcinoma were treated surgically at Chang-Gung Memorial Hospital between 1977 and 1994. Among them, 106 patients (65.4%) had associated hepatolithiasis (PCC + HL group), and the remaining 56 patients (34.6%) did not (the PCC − HL group). The differences in demographics, symptomatology, laboratory data, tumor staging, histological pattern, resectability rates, and long-term survival of these two groups were compared. The male to female ratio was 0.7 in the PCC + HL group and 1.3 in the PCC − HL group (P 〈 0.05). Two thirds of the PCC + HL group presented with acute cholangitis, whereas two thirds of the PCC − HL group presented with hepatomegaly (P 〈 0.01). Those patients in the PCC + HL group were in earlier stages than those of the PCC − HL group at the time of the initial diagnosis (P 〈 0.05). The resectability rate for the PCC + HL group was 31.1% and for the PCC − HL group, 26.8% (P 〉 0.05). Surgical mortality rates were 3.8% in the PCC + HL group and 3.6% in the PCC − HL group (P 〉 0.05). The morbidity rate was much higher in the PCC + HL group than in the PCC − HL group (P 〈 0.01). The 1-, 3-, and 5-year survival rates were 35.5%, 20.5%, and 16.5% in the PCC + HL group and 27.2%, 8.8%, and 7.8% in the PCC − HL group (P 〉 0.05). In conclusion, the presence of hepatolithiasis hindered an exact diagnosis of underlying cholangiocarcinoma preoperatively, precipitated biliary sepsis which affected resectability, and increased postoperative morbidity. Hepatolithiasis per se, however, did not influence the long-term survival.
    Type of Medium: Electronic Resource
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