Imaging Features of Hepatocellular Carcinoma After Transcatheter Arterial Chemoembolization and Radiofrequency Ablation
Hyo Soon Lim1,
Yong Yeon Jeong1,
Heoung Keun Kang1,
Jae Kyu Kim2 and
Jin Gyoon Park2
1 Department of Diagnostic Radiology, Chonnam National University Medical School
and Chonnam National University Hwasun Hospital, 160 Ilsim-ri, Hwasun-eup,
Hwasun-gun, Jeollanam-do 519-809, South Korea.
2 Department of Diagnostic Radiology, Chonnam National University Medical School
and Chonnam National University Hospital, Gwangju, South Korea.

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Fig. 1A Four types (with type I broken down into two parts) of
accumulation patterns of iodized oil on CT after transcatheter arterial
chemoembolization. Greater amount of accumulation of iodized oil within tumor
indicates greater area of necrosis. Type Ia, seen in 60-year-old man, has
homogeneous accumulation, with accumulation also seen around tumor.
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Fig. 1B Four types (with type I broken down into two parts) of
accumulation patterns of iodized oil on CT after transcatheter arterial
chemoembolization. Greater amount of accumulation of iodized oil within tumor
indicates greater area of necrosis. Type Ib, seen in 59-year-old man, has
homogeneous accumulation with accumulation not seen around tumor.
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Fig. 1C Four types (with type I broken down into two parts) of
accumulation patterns of iodized oil on CT after transcatheter arterial
chemoembolization. Greater amount of accumulation of iodized oil within tumor
indicates greater area of necrosis. Type II, seen in 73-year-old man, has
partial defect in accumulation.
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Fig. 1D Four types (with type I broken down into two parts) of
accumulation patterns of iodized oil on CT after transcatheter arterial
chemoembolization. Greater amount of accumulation of iodized oil within tumor
indicates greater area of necrosis. Type III, seen in 65-year-old woman, has
faint accumulation.
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Fig. 1E Four types (with type I broken down into two parts) of
accumulation patterns of iodized oil on CT after transcatheter arterial
chemoembolization. Greater amount of accumulation of iodized oil within tumor
indicates greater area of necrosis. Type IV, seen in 70-year-old man, has no
or slight accumulation.
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Fig. 2A 56-year-old man with residual viable tumor that shows faint
accumulation of iodized oil after transcatheter arterial chemoembolization
(TACE). On follow-up unenhanced CT scan 3 weeks after TACE, faint accumulation
of iodized oil (arrow) within tumor is seen.
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Fig. 2B 56-year-old man with residual viable tumor that shows faint
accumulation of iodized oil after transcatheter arterial chemoembolization
(TACE). Arterial phase CT scan shows contrast enhancement (arrow)
around faint accumulation of iodized oil, suggesting remaining viable
tumor.
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Fig. 2C 56-year-old man with residual viable tumor that shows faint
accumulation of iodized oil after transcatheter arterial chemoembolization
(TACE). Subsequent angiogram shows hypervascular mass (arrows) in
hepatic dome. Because of this finding, TACE was repeated.
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Fig. 3A 54-year-old man with residual viable tumor with defective
accumulation of iodized oil after transcatheter arterial chemoembolization
(TACE). On unenhanced CT scan 3 weeks after TACE, defective accumulation of
iodized oil (arrows) within tumor is seen.
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Fig. 3B 54-year-old man with residual viable tumor with defective
accumulation of iodized oil after transcatheter arterial chemoembolization
(TACE). Arterial phase CT scan shows contrast enhancement (arrows)
within defective uptake of iodized oil, suggesting remaining viable tumor.
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Fig. 4A 66-year-old woman with residual viable tumor after
transcatheter arterial chemoembolization. On unenhanced CT scan, dense
intratumoral retention of iodized oil (arrow) is shown with
beam-hardening artifact.
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Fig. 4B 66-year-old woman with residual viable tumor after
transcatheter arterial chemoembolization. On arterial phase CT scan, contrast
enhancement of tumor (arrow) is unclear.
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Fig. 4C 66-year-old woman with residual viable tumor after
transcatheter arterial chemoembolization. Axial T1-weighted gradient-echo
(TR/TE, 120/4.2) MR image shows hyperintense lesion (arrow).
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Fig. 4D 66-year-old woman with residual viable tumor after
transcatheter arterial chemoembolization. Axial T2-weighted single-shot fast
spin-echo (infinite/92) MR image shows heterogeneous hyperintense lesion.
Necrotic lesions (arrowheads) have higher signal intensity than do
viable lesions (arrow).
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Fig. 4E 66-year-old woman with residual viable tumor after
transcatheter arterial chemoembolization. On gradient-echo (180/1.8)
T1-weighted MR images after administration of gadolinium chelates, residual
viable tumor (arrow) shows intense enhancement in arterial phase
(E) and washout in delayed phase (F). Necrotic lesion
(arrowheads) shows no enhancement in either phase.
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Fig. 4F 66-year-old woman with residual viable tumor after
transcatheter arterial chemoembolization. On gradient-echo (180/1.8)
T1-weighted MR images after administration of gadolinium chelates, residual
viable tumor (arrow) shows intense enhancement in arterial phase
(E) and washout in delayed phase (F). Necrotic lesion
(arrowheads) shows no enhancement in either phase.
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Fig. 5A 64-year-old man with complete necrosis of hepatocellular
carcinoma after transcatheter arterial chemoembolization. Axial T1-weighted
gradient-echo (TR/TE, 120/4.2) MR image shows hyperintense lesion
(arrow).
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Fig. 5B 64-year-old man with complete necrosis of hepatocellular
carcinoma after transcatheter arterial chemoembolization. Axial T2-weighted
single-shot fast spin-echo (infinite/92) MR image shows hypointense lesion
(arrow), which represents coagulation necrosis. Compact uptake of
iodized oil is seen within tumor on CT (not shown).
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Fig. 6A 74-year-old man with incomplete necrosis of hepatocellular
carcinoma after transcatheter arterial chemoembolization (TACE). On follow-up
unenhanced CT scan 3 weeks after TACE, defective accumulation of iodized oil
(arrow) within tumor is seen.
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Fig. 6B 74-year-old man with incomplete necrosis of hepatocellular
carcinoma after transcatheter arterial chemoembolization (TACE). Arterial
phase CT scan shows contrast enhancement (arrow) within lesion.
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Fig. 6C 74-year-old man with incomplete necrosis of hepatocellular
carcinoma after transcatheter arterial chemoembolization (TACE).
Contrast-enhanced sonography clearly shows enhancement of lesion
(arrows) irrespective of accumulation of iodized oil on CT.
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Fig. 7A 70-year-old man with successful radiofrequency ablation.
Arterial phase CT scan 1 day after radiofrequency ablation shows unenhanced
oval ablated lesion (arrow).
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Fig. 7B 70-year-old man with successful radiofrequency ablation.
Axial T1-weighted gradient-echo (TR/TE, 180/1.8) MR image 2 months after
radiofrequency ablation shows oval ablated lesion (arrow) with high
signal intensity relative to surrounding liver parenchyma.
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Fig. 7C 70-year-old man with successful radiofrequency ablation.
Axial T2-weighted fast spin-echo (7,500/90) MR image shows oval ablated lesion
(arrow) with low signal intensity relative to surrounding liver
parenchyma, representing coagulative necrosis. Note high-signal-intensity rim
(arrowheads) representing reactive change.
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Fig. 7D 70-year-old man with successful radiofrequency ablation. On
T1-weighted MR image after administration of gadolinium chelates, ablated
lesion (arrow) shows lack of enhancement, although high signal
intensity on unenhanced MR image interferes with proper evaluation of arterial
phase enhancement.
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Fig. 8A 62-year-old man with residual tumor after radiofrequency
ablation. On follow-up CT scan 2 months after radiofrequency ablation,
arterial phase CT scan shows nodular enhancement (arrowheads) at
anterior aspect of ablated lesion (arrow).
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Fig. 8B 62-year-old man with residual tumor after radiofrequency
ablation. Delayed phase CT scan shows washout of nodular enhancement
(arrowhead) around ablated lesion (arrow). Nodule was
thought to represent residual viable tumor and was treated with repeat
radiofrequency ablation.
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Fig. 9A 55-year-old man with successful radiofrequency ablation.
Arterial phase CT scan 1 day after radiofrequency ablation shows oval-shaped
ablated lesion (arrow) with surrounding hyperemia
(arrowheads).
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Fig. 9B 55-year-old man with successful radiofrequency ablation. On
follow-up CT scan 8 months later, ablated lesion (arrow) shows no
contrast enhancement and interval decrease in size.
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Fig. 10A 80-year-old man with residual viable tumor after
radiofrequency ablation. Axial T1-weighted gradient-echo (TR/TE, 180/4.2) MR
image 2 months after radiofrequency ablation shows hypointense lesion
(arrow).
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Fig. 10B 80-year-old man with residual viable tumor after
radiofrequency ablation. Axial T2-weighted fast spin-echo (500/91) MR image
shows hyperintense lesion (arrow) that represents viable tumor.
Bright signal intensity is seen in peripheral portion (arrowhead) of
ablated lesion, representing necrosis.
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Fig. 10C 80-year-old man with residual viable tumor after
radiofrequency ablation. On axial T1-weighted MR image after administration of
gadolinium chelates, ablated lesion (arrow) shows peripheral area of
enhancement (arrowheads), suggesting residual viable tumor.
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Fig. 11A 73-year-old man with marginal recurrent tumor after
radiofrequency ablation. Follow-up CT scan 8 months after radiofrequency
ablation shows small enhancing nodule (arrowheads) at posterior
aspect of ablated lesion (arrow), representing marginal recurrent
tumor.
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Fig. 11B 73-year-old man with marginal recurrent tumor after
radiofrequency ablation. Contrast-enhanced sonography also shows focal flow
signals (arrowheads) that represent recurrent tumor vessels within
ablated area (arrow). Recurred tumor was treated with repeat
radiofrequency ablation.
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Copyright © 2006 by the American Roentgen Ray Society.