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1998
DOI: 10.1001/archsurg.133.5.510
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Evaluation of Benign vs Malignant Hepatic Lesions With Positron Emission Tomography

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Cited by 286 publications
(169 citation statements)
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“…Soft-tissue masses in conjunction with focally increased glucose metabolism above the surrounding tissue level were regarded as malignant. A maximum standardized uptake value (SUVmax) of more than 2.5 (for extrahepatic lesions) and 3.5 (intrahepatic lesions) supported the diagnosis of a malignant lesion but was always considered in conjunction with the qualitative appearance of the lesion (e.g., a liver lesion with a SUVmax of 3.1 clearly demarcated from the background liver activity was considered malignant) (12).…”
Section: Image Evaluationmentioning
confidence: 99%
“…Soft-tissue masses in conjunction with focally increased glucose metabolism above the surrounding tissue level were regarded as malignant. A maximum standardized uptake value (SUVmax) of more than 2.5 (for extrahepatic lesions) and 3.5 (intrahepatic lesions) supported the diagnosis of a malignant lesion but was always considered in conjunction with the qualitative appearance of the lesion (e.g., a liver lesion with a SUVmax of 3.1 clearly demarcated from the background liver activity was considered malignant) (12).…”
Section: Image Evaluationmentioning
confidence: 99%
“…The widely accepted imaging modalities for staging HCC are dynamic computed tomography (CT) and contrast-enhanced magnetic resonance imaging (MRI) (5). However, CT and MRI have a limited ability to identify distant metastases (6). Previous studies have reported the role of 18 F-fluorodeoxyglucose positron emission tomography/computed tomography ( 18 F-FDG-PET/CT) in detecting distant metastasis in a variety of malignancies (7).…”
Section: Introductionmentioning
confidence: 99%
“…In our case, foci of increased 18 F-FDG uptake in the transplanted liver were concerning for malignancy but were found to be benign inflammatory and ischemic changes including large bile duct necrosis, acute cholangitis, bile duct obstruction changes and periportal fibrosis. In non-transplanted liver, several non-malignant processes have been described to take up 18 F-FDG including: intrahepatic cholestasis (8), acute cholangitis (9,10), sclerosing cholangitis (11), liver abscess (12,13), hepatic pseudotumor (14), and hepatic sarcoidosis (15).…”
Section: Figurementioning
confidence: 99%