- •Foreword I
- •Foreword II
- •Preface
- •Contents
- •1 Abscesses – Pyogenic Type
- •3 Cyst I – Typical Small
- •4 Cyst II – Typical Large with MR-CT Correlation
- •5 Cyst III – Multiple Small Lesions with MR-CT-US Comparison
- •6 Cyst IV – Adult Polycystic Liver Disease
- •7 Cystadenoma / Cystadenocarcinoma
- •8 Hemangioma I – Typical Small
- •10 Hemangioma III – Typical Giant
- •11 Hemangioma IV – Giant Type with a Large Central Scar
- •13 Hemangioma VI – Multiple with Perilesional Enhancement
- •14 Hemorrhage
- •16 Mucinous Metastasis – Mimicking an Hemangioma
- •17 Colorectal Metastases I – Typical Lesion
- •18 Colorectal Metastases II – Typical Multiple Lesions
- •19 Colorectal Metastases III – Metastasis Versus Cyst
- •20 Colorectal Metastases IV – Metastasis Versus Hemangiomas
- •21 Liver Metastases V – Large, Mucinous, Mimicking a Primary Liver Lesion
- •24 Breast Carcinoma Liver Metastases
- •25 Kahler’s Disease (Multiple Myeloma) Liver Metastases
- •26 Melanoma Liver Metastases I – Focal Type
- •27 Melanoma Liver Metastases II – Diffuse Type
- •28 Neuroendocrine Tumor I – Typical Liver Metastases
- •29 Neuroendocrine Tumor II – Pancreas Tumor Metastases
- •30 Neuroendocrine Tumor III – Gastrinoma Liver Metastases
- •31 Neuroendocrine Tumor IV – Carcinoid Tumor Liver Metastases
- •32 Neuroendocrine Tumor V – Peritoneal Spread
- •34 Renal Cell Carcinoma Liver Metastasis
- •35 Cirrhosis I – Liver Morphology
- •36 Cirrhosis II – Regenerative Nodules and Confluent Fibrosis
- •37 Cirrhosis III – Dysplastic Nodules
- •38 Cirrhosis IV – Dysplastic Nodules – HCC Transition
- •39 Cirrhosis V – Cyst in a Cirrhotic Liver
- •40 Cirrhosis VI – Multiple Cysts in a Cirrhotic Liver
- •41 Cirrhosis VII – Hemangioma in a Cirrhotic Liver
- •42 HCC in Cirrhosis I – Typical Small with Pathologic Correlation
- •43 HCC in Cirrhosis II – Small With and Without a Tumor Capsule
- •44 HCC in Cirrhosis III – Nodule-in-Nodule Appearance
- •45 HCC in Cirrhosis IV – Mosaic Pattern with Pathologic Correlation
- •47 HCC in Cirrhosis VI – Mosaic Pattern with Fatty Infiltration
- •48 HCC in Cirrhosis VII – Large Growing Lesion with Portal Invasion
- •49 HCC in Cirrhosis VIII – Segmental Diffuse with Portal Vein Thrombosis
- •50 HCC in Cirrhosis IX – Multiple Lesions Growing on Follow-up
- •51 HCC in Cirrhosis X – Capsular Retraction and Suspected Diaphragm Invasion
- •52 HCC in Cirrhosis XI – Diffuse Within the Entire Liver with Portal Vein Thrombosis
- •53 HCC in Cirrhosis XII – With Intrahepatic Bile Duct Dilatation
- •54 Focal Nodular Hyperplasia I – Typical with Large Central Scar and Septa
- •55 Focal Nodular Hyperplasia II – Typical with Pathologic Correlation
- •57 Focal Nodular Hyperplasia IV – Multiple FNH Syndrome
- •58 Focal Nodular Hyperplasia V – Fatty FNH with Concurrent Fatty Adenoma
- •59 Focal Nodular Hyperplasia VI – Atypical with T2 Dark Central Scar
- •60 Hepatic Angiomyolipoma – MR-CT Comparison
- •61 Hepatic Lipoma – MR-CT-US Comparison
- •62 Hepatocellular Adenoma I – Typical with Pathologic Correlation
- •63 Hepatocellular Adenoma II – Large Exophytic with Pathologic Correlation
- •64 Hepatocellular Adenoma III – Typical Fat-Containing
- •65 Hepatocellular Adenoma IV – With Large Hemorrhage
- •77 Intrahepatic Cholangiocarcinoma – With Pathologic Correlation
- •78 Telangiectatic Hepatocellular Lesion
- •79 Focal Fatty Infiltration Mimicking Metastases
- •80 Focal Fatty Sparing Mimicking Liver Lesions
- •81 Hemosiderosis – Iron Deposition, Acquired Type
- •82 Hemochromatosis – Severe Type
- •83 Hemochromatosis with Solitary HCC
- •84 Hemochromatosis with Multiple HCC
- •85 Thalassemia with Iron Deposition
- •86 Arterioportal Shunt I – Early Enhancing Lesion in a Cirrhotic Liver
- •89 Budd-Chiari Syndrome II – Gradual Deformation of the Liver
- •90 Budd-Chiari Syndrome III – Nodules Mimicking Malignancy
- •92 Caroli’s Disease I – Intrahepatic with Segmental Changes
- •93 Caroli’s Disease II – Involvement of the Liver and Kidneys
- •95 Choledocholithiasis (Bile Duct Stones)
- •96 Gallbladder Carcinoma I – Versus Gallbladder Wall Edema
- •97 Gallbladder Carcinoma II – Hepatoid Type of Adenocarcinoma
- •98 Hilar Cholangiocarcinoma I – Typical
- •99 Hilar Cholangiocarcinoma II – Intrahepatic Mass
- •100 Hilar Cholangiocarcinoma III – Partially Extrahepatic Tumor
- •101 Hilar Cholangiocarcinoma IV – Metal Stent with Interval Growth
- •102 Hilar Cholangiocarcinoma V – Biliary Dilatation Mimicking Klatskin Tumor at CT
- •103 Primary Sclerosing Cholangitis I – Cholangitis and Segmental Atrophy
- •104 Primary Sclerosing Cholangitis II – With Intrahepatic Cholestasis
- •105 Primary Sclerosing Cholangitis III – With Intrahepatic Stones
- •106 Primary Sclerosing Cholangitis IV – With Biliary Cirrhosis
- •107 Primary Sclerosing Cholangitis V – With Intrahepatic Cholangiocarcinoma
- •108 Primary Sclerosing Cholangitis VI – With Hilar Cholangiocarcinoma
- •109 T2 Bright Liver Lesions
- •110 T1 Bright Liver Lesions
- •111 T2 Bright Central Scar
- •112 Lesions in Fatty Liver
- •113 Appendix I: MR Imaging Technique and Protocol
- •114 Appendix II: Liver Segmental and Vascular Anatomy
- •Subject Index
112 Part IIC – Primary Solid Liver Lesions in Cirrhotic Liver
53 HCC in Cirrhosis XII – With Intrahepatic Bile Duct Dilatation
Hepatocellular carcinomas (HCCs) rarely may show invasion with dilatation of the bile ducts and cause jaundice mimicking an intrahepatic cholangiocarcinoma. The treatment options and prognosis may differ. Therefore, early distinction is important. Intraductal cholangiocarcinoma is frequently limited to the mucosa but can invade the ductal wall at a late stage. It usually follows a relatively benign course, and long-term survival can usually be expected after complete surgical resection. In contrast, the bile duct invasion is a late and rare presentation in HCC with a relatively poor prognosis. Definitive surgical intervention is often not feasible because of tumor extension and associated advanced liver cirrhosis.
MR Imaging Findings
At MR imaging, segmental dilatation of the bile ducts in combination with a liver mass may suggest the presence of a cholangiocarcinoma. However, the history of parenchymal liver disease with cirrhosis may strongly indicate the presence of an underlying HCC. Also the mosaic pattern, tumor capsular enhancement, and portal vein thrombosis are indicators of HCC. In rare cases, several intrahepatic confluent nodules of HCC may be present that may also show intrahepatic bile duct dilatation. Such HCCs may be unusually bright on T2-weighted images and show intense arterial enhancement (Figs. 53.1 – 53.3).
Differential Diagnosis
The differential diagnosis should include (1) cholangiocarcinoma,
(2)primary sclerosing cholangitis with a cholangiocarcinoma, and
(3)liver metastases of a hepatoid type of stomach or gallbladder tumor, which often have an elevated alpha-fetoprotein value and clinically mimic HCC.
Management
Percutaneous biliary drainage and transarterial chemoembolization may be used for palliation.
Literature
1.Jung AY, Lee JM, Choi SH, et al. (2006) Computed tomography features of an intraductal polypoid mass differentiation between hepatocellular carcinoma with bile duct tumor invasion and intraductal papillary cholangiocarcinoma. JCAT 30:18 – 24
2.Kojiro M, Kawabata K, Kawano Y, et al. (1982) Hepatocellular carcinoma presenting as intrabile duct tumor growth: a clinicopathologic study of 24 cases. Cancer 49:2144 – 2147
3.Tamada K, Isoa N, Wada S, et al. (2001) Intraductal ultrasonography for hepatocellular carcinoma with tumor thrombi in the bile duct; comparison with polypoid cholangiocarcinoma. J Gastroenterol Hepatol 16:801 – 805
4.Lauffer JM, Mai G, Berchtold D, et al. (1999) Multidisciplinary approach to palliation of obstructive jaundice caused by a central hepatocellular carcinoma. Dig Surg 16:531 – 536
53 HCC in Cirrhosis XII – With Intrahepatic Bile Duct Dilatation 113
Fig. 53.1. HCC, with dilated bile ducts in a cirrhotic liver, drawings. SSTSE: HCC is slightly hyperintense to the liver and causes compression, encasement, and dilatation of the bile ducts; T1 in-phase: HCC is almost isointense to the
Fig. 53.2. HCC, dilated bile ducts in a cirrhotic liver, MRI findings. A Axial SSTSE image (SSTSE): HCC is slightly hyperintense and causes compression, encasement, and dilatation of the bile ducts (arrow). B Axial in-phase image (T1 in-phase): HCC is isointense to the liver. C Axial arterial phase image (ART): HCC shows faint heterogeneous enhancement. D Axial delayed phase image (DEL): HCC shows washout without any enhancing tumor cap-
liver; ART: HCC shows faint heterogeneous enhancement; DEL: HCC shows washout without a tumor capsule
sule. E Coronal reformat based on the axial delayed phase image (MRCP – dark lumen) shows dark, dilated bile ducts in an enhanced liver. F Coronal SSTSE image (SSTSE) shows the enlarged spleen indicating portal hypertension. G Coronal delayed phase image (DEL) shows unenhanced dilated bile ducts in the left liver with normal common bile duct (arrow). H Drawing shows HCC with dilated bile ducts
Fig. 53.3. HCC, dilated bile ducts, MRI findings in another patient with increased alpha-fetoprotein. A Coronal SSTSE image (SSTSE) shows a large multifocal HCC with interspersed dilated bile ducts. B Axial SSTSE image (SSTSE) of
the massive HCC with dilated bile ducts. C Axial arterial phase image (ART) shows intense enhancement of the nodules within HCC. D Axial delayed phase image (DEL) shows washout with septa enhancement
Part II/IID
Solid Liver Lesions |
II |
Primary Solid Liver Lesions in Non-Cirrhotic Liver |
IIB |