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PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 97-483 OBJECTIVE denotes The detection of increased fluorine-18 fluorodeoxyglucose (18F-FDG) uptake by positron emission tomography (PET) is based on the enhanced glucose metabolism of tumor cells. Because the detection and staging of hepatocellular carcinoma (HCC) in patients with liver cirrhosis can be difficult, we prospectively evaluated the sensitivity of 18F-FDG PET in 14 consecutive patients with HCC.
T2 493-729 METHODS denotes Whole body and regional 18F-FDG PET of the liver were obtained. The results were compared with ultrasonography, contrast-enhanced, helical CT, histological grading, p53 protein expression of HCC, and serum alpha-fetoprotein (AFP) level.
T3 739-1515 RESULTS denotes In 7 patients PET demonstrated increased tumor 18F-FDG uptake, whereas HCC was not distinguishable from nonmalignant liver tissue in 7 other patients. Hepatic lesions were detected by ultrasonography in all patients, whereas only 11 of 14 HCCs could be identified by CT. In 3 patients extrahepatic spread was demonstrated by 18F-FDG PET. Patients with increased tumor 18F-FDG uptake had significantly larger hepatic lesions and higher serum AFP levels than those with normal 18F-FDG uptake. Lesions could be visualized by 18F-FDG PET in 7 of 8 patients with moderately or poorly differentiated HCC, whereas none of the six well-differentiated tumors was detected. Two patients with strong p53 expression demonstrated increased tumor 18F-FDG uptake and extrahepatic metastases.
T4 1529-1777 CONCLUSIONS denotes The sensitivity of 18F-FDG PET for the imaging of HCC is low. Nevertheless, in patients with moderately or poorly differentiated HCC, tumors >5 cm, or with markedly elevated AFP levels 18F-FDG PET may contribute to an effective noninvasive staging.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 257-262 HP_0002664 denotes tumor
T2 307-331 HP_0001402 denotes hepatocellular carcinoma
T3 361-370 HP_0001394 denotes cirrhosis

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10566736-0#12#15#gene23583 158-163 gene23583 denotes F-FDG
10566736-0#60#84#diseaseC2239176 702-1194 diseaseC2239176 denotes ha-fetoprotein (AFP) level. RESULTS: In 7 patients PET demonstrated increased tumor 18F-FDG uptake, whereas HCC was not distinguishable from nonmalignant liver tissue in 7 other patients. Hepatic lesions were detected by ultrasonography in all patients, whereas only 11 of 14 HCCs could be identified by CT. In 3 patients extrahepatic spread was demonstrated by 18F-FDG PET. Patients with increased tumor 18F-FDG uptake had significantly larger hepatic lesions and higher serum AFP levels tha
10566736-10#25#28#gene7157 1428-1431 gene7157 denotes p53
10566736-10#73#76#gene23583 1476-1479 gene23583 denotes FDG
10566736-10#101#111#diseaseC0027627 1504-1514 diseaseC0027627 denotes metastases
10566736-4#101#104#gene7157 658-661 gene7157 denotes p53
10566736-4#127#130#diseaseC2239176 684-687 diseaseC2239176 denotes HCC
12#15#gene2358360#84#diseaseC2239176 10566736-0#12#15#gene23583 10566736-0#60#84#diseaseC2239176 associated_with F-FDG,"ha-fetoprotein (AFP) level. RESULTS: In 7 patients PET demonstrated increased tumor 18F-FDG uptake, whereas HCC was not distinguishable from nonmalignant liver tissue in 7 other patients. Hepatic lesions were detected by ultrasonography in all patients, whereas only 11 of 14 HCCs could be identified by CT. In 3 patients extrahepatic spread was demonstrated by 18F-FDG PET. Patients with increased tumor 18F-FDG uptake had significantly larger hepatic lesions and higher serum AFP levels tha"
25#28#gene7157101#111#diseaseC0027627 10566736-10#25#28#gene7157 10566736-10#101#111#diseaseC0027627 associated_with p53,metastases
73#76#gene23583101#111#diseaseC0027627 10566736-10#73#76#gene23583 10566736-10#101#111#diseaseC0027627 associated_with FDG,metastases
101#104#gene7157127#130#diseaseC2239176 10566736-4#101#104#gene7157 10566736-4#127#130#diseaseC2239176 associated_with p53,HCC

DisGeNET

Id Subject Object Predicate Lexical cue
T0 439-442 gene:23583 denotes FDG
T1 978-981 disease:C2239176 denotes HCC
R1 T0 T1 associated_with FDG,HCC