1.Tumor Response Evaluation after Treatment and Post-treatment Surveillance of Hepatocellular Carcinoma
Journal of Liver Cancer 2018;18(1):9-16
Hepatocellular carcinoma is one of the most prevalent malignancies and frequent causes of death worldwide. Treatment options of hepatocellular carcinoma consist of locoregional therapy, surgical resection, liver transplantation, and systemic therapy. Assessment of tumor response is required in patients receiving locoregional and systemic therapy. The Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 is widely used tumor response evaluation criteria. However, the RECIST does not reflect the extent of tumor necrosis after some locoregional therapies and molecular targeted agents. The Modified RECIST (mRECIST), which has the concept of viable tumor, was introduced in order to overcome this problem. The mRECIST were developed on the basis of RECIST version 1.1 and only tumoral tissue showing contrast uptake in arterial phase of dynamic radiologic imaging techniques was measured to assess tumor response. Recently, immune checkpoint inhibitors have emerged as a promising therapeutic modality for the treatment of hepatocellular carcinoma. To identify tumor response after immunotherapy, immune RECIST (iRECIST) has been proposed as consensusbased criteria. After achieving complete response after curative treatment, optimal surveillance was needed to detect recurrence. Individualized surveillance schedule should be considered, taking into consideration the risk factors of the patient and the risk associated with the treatment modalities.
Appointments and Schedules
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Carcinoma, Hepatocellular
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Cause of Death
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Humans
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Immunotherapy
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Liver Transplantation
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Necrosis
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Prognosis
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Radiography
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Recurrence
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Response Evaluation Criteria in Solid Tumors
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Risk Factors
2.MRI Features of Hepatocellular Carcinoma Related to Biologic Behavior.
Korean Journal of Radiology 2015;16(3):449-464
Imaging studies including magnetic resonance imaging (MRI) play a crucial role in the diagnosis and staging of hepatocellular carcinoma (HCC). Several recent studies reveal a large number of MRI features related to the prognosis of HCC. In this review, we discuss various MRI features of HCC and their implications for the diagnosis and prognosis as imaging biomarkers. As a whole, the favorable MRI findings of HCC are small size, encapsulation, intralesional fat, high apparent diffusion coefficient (ADC) value, and smooth margins or hyperintensity on the hepatobiliary phase of gadoxetic acid-enhanced MRI. Unfavorable findings include large size, multifocality, low ADC value, non-smooth margins or hypointensity on hepatobiliary phase images. MRI findings are potential imaging biomarkers in patients with HCC.
Aged
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Biological Products
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Biomarkers, Tumor
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Carcinoma, Hepatocellular/diagnosis/pathology/*radiography
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Contrast Media
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Gadolinium DTPA
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Humans
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Liver Neoplasms/diagnosis/pathology/*radiography
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Magnetic Resonance Imaging/*methods
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Male
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Middle Aged
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Neoplasm Staging/methods
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Prognosis
3.Imaging findings of mimickers of hepatocellular carcinoma.
Tae Kyoung KIM ; Eunchae LEE ; Hyun Jung JANG
Clinical and Molecular Hepatology 2015;21(4):326-343
Radiological imaging plays a crucial role in the diagnosis of hepatocellular carcinoma (HCC) as the noninvasive diagnosis of HCC in high-risk patients by typical imaging findings alone is widely adopted in major practice guidelines for HCC. While imaging techniques have markedly improved in detecting small liver lesions, they often detect incidental benign liver lesions and non-hepatocellular malignancy that can be misdiagnosed as HCC. The most common mimicker of HCC in cirrhotic liver is nontumorous arterioportal shunts that are seen as focal hypervascular liver lesions on dynamic contrast-enhanced cross-sectional imaging. Rapidly enhancing hemangiomas can be easily misdiagnosed as HCC especially on MR imaging with liver-specific contrast agent. Focal inflammatory liver lesions mimic HCC by demonstrating arterial-phase hypervascularity and subsequent washout on dynamic contrast-enhanced imaging. It is important to recognize the suggestive imaging findings for intrahepatic cholangiocarcinoma (CC) as the management of CC is largely different from that of HCC. There are other benign mimickers of HCC such as angiomyolipomas and focal nodular hyperplasia-like nodules. Recognition of their typical imaging findings can reduce false-positive HCC diagnosis.
Carcinoma, Hepatocellular/*diagnosis/radiography
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Diagnosis, Differential
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Hemangioma/complications/radiography/ultrasonography
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Hepatitis B/complications
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Humans
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Inflammation/radiography/ultrasonography
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Liver/radiography/ultrasonography
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Liver Cirrhosis/complications/radiography
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Liver Neoplasms/*diagnosis/radiography
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Magnetic Resonance Imaging
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Non-alcoholic Fatty Liver Disease/radiography/ultrasonography
4.Spontaneous Neoplastic Remission of Hepatocellular Carcinoma.
Sung Bae KIM ; Wonseok KANG ; Seung Hwan SHIN ; Hee Seung LEE ; Sang Hoon LEE ; Gi Hong CHOI ; Jun Yong PARK
The Korean Journal of Gastroenterology 2015;65(5):312-315
We report on a case of a 57-year-old male who underwent a curative resection for hepatocellular carcinoma (HCC) with histological confirmation of a spontaneously necrotized tumor. Initial serum AFP level was 4,778 ng/mL. A 3.7 cm hyperechoic mass in segment 6 of the liver was observed on ultrasonography and dynamic contrast-enhanced liver MRI showed a 3.7x3.1 cm sized HCC. He was scheduled to undergo curative surgical resection under the clinical diagnosis of an early stage HCC (Barcelona Clinic Liver Cancer stage A). Without treatment, the serum AFP level declined rapidly to 50 ng/mL over five weeks. He underwent curative wedge resection of segment 6 of the liver. Histology revealed complete necrosis of the mass rimmed by inflamed fibrous capsule on a background of HBV-related cirrhosis with infiltration of lymphoplasma cells. Exact pathophysiology underlying this event is unknown. Among the proposed mechanisms of spontaneous neoplastic remission of HCC, circulatory disturbance and activation of host immune response offer the most scientific explanation for the complete histologic necrosis of HCC in the resected mass seen in our patient.
Carcinoma, Hepatocellular/*diagnosis/diagnostic imaging/pathology
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Hepatitis B/complications/diagnosis
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Humans
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Liver/diagnostic imaging/pathology
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Liver Cirrhosis/etiology
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Liver Neoplasms/*diagnosis/diagnostic imaging/pathology
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Magnetic Resonance Imaging
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Male
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Middle Aged
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Necrosis
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Radiography
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Remission, Spontaneous
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Ultrasonography
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alpha-Fetoproteins/analysis
5.Does Establishing a Safety Margin Reduce Local Recurrence in Subsegmental Transarterial Chemoembolization for Small Nodular Hepatocellular Carcinomas?.
Hyo Jin KANG ; Young Il KIM ; Hyo Cheol KIM ; Hwan Jun JAE ; Saebeom HUR ; Jin Wook CHUNG
Korean Journal of Radiology 2015;16(5):1068-1078
OBJECTIVE: To test the hypothesis that a safety margin may affect local tumor recurrence (LTR) in subsegmental chemoembolization. MATERIALS AND METHODS: In 101 patients with 128 hepatocellular carcinoma (HCC) nodules (1-3 cm in size and < or = 3 in number), cone-beam CT-assisted subsegmental lipiodol chemoembolization was performed. Immediately thereafter, a non-contrast thin-section CT image was obtained to evaluate the presence or absence of intra-tumoral lipiodol uptake defect and safety margin. The effect of lipiodol uptake defect and safety margin on LTR was evaluated. Univariate and multivariate analyses were performed to indentify determinant factors of LTR. RESULTS: Of the 128 HCC nodules in 101 patients, 49 (38.3%) nodules in 40 patients showed LTR during follow-up period (median, 34.1 months). Cumulative 1- and 2-year LTR rates of nodules with lipiodol uptake defect (n = 27) and those without defect (n = 101) were 58.1% vs. 10.1% and 72.1% vs. 19.5%, respectively (p < 0.001). Among the 101 nodules without a defect, the 1- and 2-year cumulative LTR rates for nodules with complete safety margin (n = 52) and those with incomplete safety margin (n = 49) were 9.8% vs. 12.8% and 18.9% vs. 19.0% (p = 0.912). In multivariate analyses, ascites (p = 0.035), indistinct tumor margin on cone-beam CT (p = 0.039), heterogeneous lipiodol uptake (p = 0.023), and intra-tumoral lipiodol uptake defect (p < 0.001) were determinant factors of higher LTR. CONCLUSION: In lipiodol chemoembolization, the safety margin in completely lipiodolized nodule without defect will not affect LTR in small nodular HCCs.
Adult
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Aged
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Carcinoma, Hepatocellular/radiography/*therapy
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Chemoembolization, Therapeutic
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Cone-Beam Computed Tomography
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Ethiodized Oil/*administration & dosage
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Female
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Follow-Up Studies
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Humans
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Liver Neoplasms/radiography/*therapy
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Male
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Middle Aged
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Multivariate Analysis
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Neoplasm Recurrence, Local/radiography
6.A case of hepatoblastoma misdiagnosed as combined hepatocellular carcinoma and cholangiocarcinoma in an adult.
Keun Woo PARK ; Chang Jin SEO ; Dae Young YUN ; Min Keun KIM ; Byung Seok KIM ; Young Seok HAN ; Hoon Kyu OH ; Chang Hyeong LEE
Clinical and Molecular Hepatology 2015;21(3):300-308
Hepatoblastoma usually occurs in children under the age of 2 years, with very few cases reported in adults. We experienced a case of adult hepatoblastoma in a 36-year-old female with chronic hepatitis B . She had experienced sudden onset abdominal pain. Her serum alpha-fetoprotein level was markedly elevated, and abdominal CT showed a 9-cm mass with internal hemorrhage in the right hepatic lobe with hemoperitoneum, so an emergency hepatic central bisectionectomy was performed. The initial histologic examination revealed that the mass mimicked combined hepatocellular carcinoma and cholangiocarcinoma with spindle-cell metaplasia of the cholangiocarcinoma element. Follow-up abdominal CT performed 3 months later showed a 5.5-cm metastatic mass in the left subphrenic area. Laparoscopic splenectomy with mass excision was performed, and hepatoblastoma was confirmed histologically. A histologic re-examination of previously obtained surgical specimens also confirmed the presence of hepatoblastoma. Metastatic hepatoblastoma was found at multiple sites of the abdomen during follow-up, and so chemotherapy with cisplatin, 5-fluorouracil (5-FU), and vincristine was applied, followed by carboplatin and doxorubicin . Despite surgery and postoperative chemotherapy, she died 12 months after symptom onset.
Adult
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Carcinoma, Hepatocellular/pathology
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Cholangiocarcinoma/pathology
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Cisplatin/therapeutic use
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Diagnostic Errors
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Doxorubicin/therapeutic use
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Drug Therapy, Combination
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Female
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Fluorouracil/therapeutic use
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Hepatitis B, Chronic/complications/diagnosis
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Hepatoblastoma/drug therapy/*pathology/radiography
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Humans
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Liver Neoplasms/drug therapy/*pathology/radiography
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Tomography, X-Ray Computed
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Vincristine/therapeutic use
7.Growth rate of early-stage hepatocellular carcinoma in patients with chronic liver disease.
Chansik AN ; Youn Ah CHOI ; Dongil CHOI ; Yong Han PAIK ; Sang Hoon AHN ; Myeong Jin KIM ; Seung Woon PAIK ; Kwang Hyub HAN ; Mi Suk PARK
Clinical and Molecular Hepatology 2015;21(3):279-286
BACKGROUND/AIMS: The goal of this study was to estimate the growth rate of hepatocellular carcinoma (HCC) and identify the host factors that significantly affect this rate. METHODS: Patients with early-stage HCC (n=175) who underwent two or more serial dynamic imaging studies without any anticancer treatment at two tertiary care hospitals in Korea were identified. For each patient, the tumor volume doubling time (TVDT) of HCC was calculated by comparing tumor volumes between serial imaging studies. Clinical and laboratory data were obtained from the medical records of the patients. RESULTS: The median TVDT was 85.7 days, with a range of 11 to 851.2 days. Multiple linear regression revealed that the initial tumor diameter (a tumor factor) and the etiology of chronic liver disease (a host factor) were significantly associated with the TVDT. The TVDT was shorter when the initial tumor diameter was smaller, and was shorter in HCC related to hepatitis B virus (HBV) infection than in HCC related to hepatitis C virus (HCV) infection (median, 76.8 days vs. 137.2 days; P=0.0234). CONCLUSIONS: The etiology of chronic liver disease is a host factor that may significantly affect the growth rate of early-stage HCC, since HBV-associated HCC grows faster than HCV-associated HCC.
Adult
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Aged
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Aged, 80 and over
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Antiviral Agents/therapeutic use
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Carcinoma, Hepatocellular/complications/*pathology/radiography
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Demography
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Female
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Hepatitis B, Chronic/*complications/drug therapy
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Hepatitis C, Chronic/*complications/drug therapy
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Humans
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Linear Models
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Liver Neoplasms/complications/*pathology/radiography
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Magnetic Resonance Imaging
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Male
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Middle Aged
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Neoplasm Staging
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Republic of Korea
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Retrospective Studies
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Tertiary Care Centers
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Tomography, X-Ray Computed
8.Role of C-Arm Cone-Beam CT in Chemoembolization for Hepatocellular Carcinoma.
Korean Journal of Radiology 2015;16(1):114-124
With the advent of C-arm cone-beam computed tomography (CBCT), minimally-invasive procedures in the angiography suite made a new leap beyond the limitations of 2-dimensional (D) angiography alone. C-arm CBCT can help interventional radiologists in several ways with the treatment of hepatocellular carcinoma (HCC); visualization of small tumors and tumor-feeding arteries, identification of occult lesion and 3D configuration of tortuous hepatic arteries, assurance of completeness of chemoembolization, suggestion of presence of extrahepatic collateral arteries supplying HCCs, and prevention of nontarget embolization. With more improvements in the technology, C-arm CBCT may be essential in all kinds of interventional procedures in the near future.
Carcinoma, Hepatocellular/radiography/*therapy
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Chemoembolization, Therapeutic
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Cone-Beam Computed Tomography
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Hepatic Artery/radiography
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Humans
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Imaging, Three-Dimensional
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Liver Neoplasms/radiography/*therapy
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Severity of Illness Index
9.Cancer Stem Cells in Primary Liver Cancers: Pathological Concepts and Imaging Findings.
Ijin JOO ; Haeryoung KIM ; Jeong Min LEE
Korean Journal of Radiology 2015;16(1):50-68
There is accumulating evidence that cancer stem cells (CSCs) play an integral role in the initiation of hepatocarcinogenesis and the maintaining of tumor growth. Liver CSCs derived from hepatic stem/progenitor cells have the potential to differentiate into either hepatocytes or cholangiocytes. Primary liver cancers originating from CSCs constitute a heterogeneous histopathologic spectrum, including hepatocellular carcinoma, combined hepatocellular-cholangiocarcinoma, and intrahepatic cholangiocarcinoma with various radiologic manifestations. In this article, we reviewed the recent concepts of CSCs in the development of primary liver cancers, focusing on their pathological and radiological findings. Awareness of the pathological concepts and imaging findings of primary liver cancers with features of CSCs is critical for accurate diagnosis, prediction of outcome, and appropriate treatment options for patients.
Bile Duct Neoplasms/pathology/radiography
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Bile Ducts, Intrahepatic/pathology/radiography
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Carcinoma, Hepatocellular/pathology/radiography
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Cholangiocarcinoma/pathology/radiography
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Humans
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Liver Neoplasms/*pathology/radiography
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Magnetic Resonance Imaging
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Neoplastic Stem Cells/*pathology/radiography
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Tomography, X-Ray Computed
10.Benign nodules mimicking hepatocellular carcinoma on gadoxetic acid-enhanced liver MRI.
Kyoung Doo SONG ; Woo Kyoung JEONG
Clinical and Molecular Hepatology 2015;21(2):187-191
No abstract available.
Adenoma, Bile Duct/pathology/*radiography
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Adult
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Aged
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Angiomyolipoma/pathology/*radiography
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Bile Duct Neoplasms/pathology/*radiography
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Bile Ducts, Intrahepatic
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Carcinoma, Hepatocellular/radiography
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Diagnosis, Differential
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Female
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Gadolinium DTPA/*chemistry
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Humans
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Liver Diseases/pathology/*radiography
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Liver Neoplasms/pathology/*radiography
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*Magnetic Resonance Imaging
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Male
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Middle Aged
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Pseudolymphoma/pathology/*radiography
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Tomography, X-Ray Computed

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