1993
DOI: 10.1007/bf00201708
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Thorotrast-induced ruptured hepatic angiosarcoma

Abstract: The use of Thorotrast as a contrast medium is now of historical interest. Thorotrast-induced angiosarcoma, though rare, still generates considerable clinical interest because of the characteristic opacification of the liver, spleen, and lymph nodes, and the long latency period between exposure and the onset of the tumor. We present a case of hepatic angiosarcoma which developed 37 years after the administration of Thorotrast.

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Cited by 14 publications
(5 citation statements)
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References 11 publications
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“…During the hepatic parenchymal phase or delayed post-contrast scans, the entire mass or at least some of its areas become isodense with normal liver (11). When typical central necrosis or hemorrhage is present substantial and prolongated peripheral enhancement may appears and may mimic a very large benign angioma in which incomplete contrast filling is a rule (2,7).…”
Section: Resultsmentioning
confidence: 99%
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“…During the hepatic parenchymal phase or delayed post-contrast scans, the entire mass or at least some of its areas become isodense with normal liver (11). When typical central necrosis or hemorrhage is present substantial and prolongated peripheral enhancement may appears and may mimic a very large benign angioma in which incomplete contrast filling is a rule (2,7).…”
Section: Resultsmentioning
confidence: 99%
“…With time, the carcinogenic effects of Th²³² became increasingly clear and numerous cases of Th²³²-related malignancies were reported, especially malignant hepatic tumours, such as hepatocellular carcinoma, cholangio carcinoma and hemangiosarcoma (HAS) (2-7). Th²³² was abandoned following a report by MacMahon et al (8) of HAS attributed to Thorotrast exposure in 1947 (6)(7)(8).…”
Section: Discussionmentioning
confidence: 99%
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“…In adults, angiosarcoma has an association with industrial exposure to vinyl chloride and has also been associated with thorotrast exposure. 32,33 On imaging studies, they usually present as solitary masses with abnormal vascularity and have been reported to cause high-output heart failure. Sarcomas may be difficult to distinguish from fibrolamellar tumors but usually lack a central stellate scar on cross-sectional imaging studies.…”
Section: Sarcomamentioning
confidence: 99%