- •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
Shahid M. Hussain · Liver MRI
Shahid M. Hussain
Liver MRI
Correlation with Other Imaging Modalities and Histopathology
Forewords by
John L. Gollan, MD, PhD and Richard C. Semelka, MD
With 114 Figures in 1.865 Parts
Shahid M. Hussain, MD, PhD Professor of Radiology Director of Body MRI
Chief Abdominal Imaging
Department of Radiology
University of Nebraska Medical Center 981045 Nebraska Medical Center Omaha, NE 68198
USA
Email: smhussain@unmc.edu
ISBN 3-540-25552-4 Springer-Verlag Berlin Heidelberg New York
Library of Congress Control Number: 2006929204
This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilm or in any other way, and storage in data banks. Duplication of this publication or parts thereof is permitted only under the provisions of the German Copyright Law of September 9, 1965, in its current version, and permission for use must always be obtained from Springer-Verlag. Violations are liable for prosecution under the German Copyright Law.
Springer is a part of Springer Science+Business Media
http://www.springer.com
Springer-Verlag Berlin Heidelberg 2007
Printed in Germany
The use of general descriptive names, registered names, trademarks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use.
Product liability: The publishers cannot guarantee the accuracy of any information about the application of operative techniques and medications contained in this book. In every individual case the user must check such information by consulting the relevant literature.
Editor: Dr. Ute Heilmann
Desk Editor: Wilma McHugh
Copy-editing: WS Editorial Ltd, Shrewsbury, UK
Production Editor: Joachim W. Schmidt
Cover design: eStudio Calamar, Spain
Typesetting: FotoSatz Pfeifer GmbH, D-82166 Gräfelfing
Printed on acid-free paper – 21/3151 – 5 4 3 2 1 0
To Ellen, Emma, and Charlotte
Foreword I
In March 1973, a short paper was published in Nature, entitled „Image formation by induced local interaction; examples employing nuclear magnetic resonance.“ The author was Paul C. Lauterbur, a Professor of Chemistry at the State University of New York at Stony Brook. In this seminal manuscript the author described a new imaging technique which moved the single dimension of NMR spectroscopy to the dual dimension of spatial orientation, thereby resulting in the foundation of modern magnetic resonance (MR) imaging. Over the ensuing years, MR imaging has assumed an increasingly important role in clinical imaging. It distinguishes itself from other imaging modalities, such as ultrasound (US) or computed tomography (CT), by the unique ability to visualize specific tissue components in a non-in- vasive manner.
In the earlier days, diagnostic MR imaging was limited to cerebral and musculoskeletal diseases. Imaging of other areas which are more prone to movement through breathing (abdominal) or pulsation motions (cardiac) became available more recently, with the introduction of faster sequences and the development of more dedicated MR imaging coils. Currently, liver MRI is considered the cornerstone of abdominal imaging. In most centers, however, liver MRI is still employed largely as a problem solving modality, when US and CT have provided an unsatisfactory outcome. This truly is an unfortunate misconception, which should be abandoned in favor of MR imaging as the primary modality for detection and characterization of liver abnormalities. If applied in the form of state-of-the-art technology, MR imaging has the potential of providing an accurate diagnosis of focal liver lesions in the majority of cases, frequently obviating the need for more invasive strategies.
We are standing on the verge of a new breakthrough in MR imaging, with the introduction of clinical high field MRI systems, such as 3.0T, multiple coil elements, parallel imaging capabilities, stronger gradients, and faster computers. Collectively, these developments will undoubtedly initiate a new era in MR imaging of the liver. The author of this impressive text, Dr. Shahid Hussain, and our institution are on the forefront of these important developments. This textbook with its numerous high quality illustrations, including computer-generated drawings, state-of-the-art MR images and radiology-pathology correlations, provides an accurate and up-to-date overview of imaging findings of a wide spectrum of liver lesions. The manner in which the contents of this book are presented provides an intuitive, easy to read approach, albeit on the topic of liver nodules or the analysis of parenchymal disorders. This textbook will be of particular benefit for clinicians and radiologists involved in the diagnosis and management of hepatic diseases.
MRI imaging will most certainly continue to emerge as a key, primary imaging modality for a broad spectrum of liver diseases. Likewise, it is essential that MRI becomes increasingly familiar to those who provide care for patients with liver abnormalities. Hence, I highly recommend this book as a routine companion for radiologists whilst reviewing MR examinations in the clinical setting, as study book for professionals in-training, such as radiology and gastroenterology fellows, and as reference for more experienced hepatologists, gastroenterologists, surgeons and pathologists. This is an easy way to acquire new knowledge on the topic of MR imaging.
John L. Gollan, MD, PhD, FRACP, FRCP, FACP
Dean, College of Medicine,
University of Nebraska Medical Center,
Omaha, Nebraska, USA
Foreword II
Annually, many thousands of patients worldwide undergo imaging for the workup of a suspected or known abnormality of the liver. Cross-sectional imaging modalities, such as ultrasound (US), computed tomography (CT), and magnetic resonance imaging (MRI), are utilized in most centers to assess liver abnormalities. These modalities, often used in various combinations, have fundamental differences in data acquisition and hence differences in the type of physical characteristics of tissues that they interrogate.
The major focus of this book is to describe that MR imaging is an accurate technique for the evaluation of focal liver lesions. MR imaging can also be used to evaluate diffuse hepatic diseases, hepatic vascular abnormalities (MR angiography), and biliary diseases (MR cholangiography). In the near future, it will be feasible to evaluate functional aspects of the liver through the use of one or more combinations of current fast breath hold MR imaging sequences, and MR spectroscopy, diffusion-weighted imaging, perfusion imaging and non-proton imaging. MR imaging may soon play a unique role in molecular imaging of the liver, including the specific targeting of diseased tissues, as well as providing imaging guidance for future smart drugs or cell delivery systems.
The introduction of multiple coil elements, parallel imaging, stronger gradients, and faster computers will undoubtedly increase the cranio-caudal (z-) coverage substantially. High resolution MR imaging of the abdomen and pelvis in a single exam (like CT) without the use of ionizing radiation and nephrotoxic iodine contrast media will become a reality. Liver MRI, however, will remain a crucial part of such a strategy that is important for staging malignancies in the abdomen.
By nature MR imaging is considered a complex modality by many radiologists and clinicians. This book succeeds in making liver MRI more accessible to the experienced as well as novice users who intend to use MR imaging for evaluation of liver abnormalities. MR imaging findings and concepts are presented and explained in simple-to-interpret computer-generated drawings. Additional explanation is provided by the radiology-pathology correlation and comparison to other imaging modalities. A particular strength of Dr. Hussain’s book is the extensive correlation with other imaging modalities, to allow the reader to have a fuller understanding of how the imaging modalities interrelate.
Shahid Hussain is one of the world’s recognized authorities on imaging of diseases of the liver. This book reveals his breadth of knowledge on this subject. Therefore, I can highly recommend this book to radiologists, clinicians, residents, radiology technicians, and students. Radiologists and radiology residents may particularly find this book useful during the reporting process of liver MR imaging exams.
Richard C. Semelka, MD
Professor and Vice-Chair of Research,
Director of MRI Services,
Department of Radiology,
University of North Carolina at Chapel Hill,
Chapel Hill, North Carolina, USA
Preface
This book provides a practical approach for MR imaging of the focal and diffuse liver lesions based on the state-of-the-art MR imaging sequences, computer-generated drawings, concise figure captions, relevant and systematic (differential) diagnostic information, recent literature references, and patient management possibilities. MR imaging findings are correlated to ultrasound, computed tomography, and pathology when appropriate. This book will greatly benefit all professionals interested and involved in imaging, diagnosis, and treatment of focal and diffuse liver lesions, including radiologists, gastroenterologists, surgeons, pathologists, MR physicists, MRI clinical scientists, radiology and other residents, MR technicians, and students.
This manuscript has especially benefited from the critical review by the following Body MR imaging experts and colleagues: Franz Sulzer, MD and Indra C. van den Bos, MD.
In addition, I am grateful to the following colleagues and friends for their continuous support during the past several years: Richard C. Semelka, MD, Donald G. Mitchell, MD, Eric K. Outwater, MD, Caroline Reinhold, MD, Mich`ele A. Brown, MD, Masayuki Kanematsu, MD, Nikolaos L. Kelekis, MD, Susan M. Ascher, MD, Sat Somers, MD, N. Cem Balci, MD, Diego R. Martin, MD, Till R. Bader, MD, PhD, Kees van Kuijk, MD, PhD, Peter M.T. Pattynama, MD, PhD, Abida Z. Ginai, MD, PhD, Jan C. den Hollander, MD, Robert A. de Man, MD, PhD, Pieter E. Zondervan, MD, Türkan Terkivatan, MD, PhD, Jan N.M. IJzermans, MD, PhD, Kees Verhoef, MD, Gabriel P. Krestin, MD, PhD, Johannes L. Bloem, MD, PhD, Reginald Goei, MD, PhD, Roy S. Dwarkasing, MD, Remy W.F. Geenen, MD, Jayant R. Kichari, MD, and Steven D. Wexner, MD, FACS, FRCS.
Finally, I am thankful to John L. Gollan, MD, PhD, Dean of the College of Medicine, and Craig W. Walker, MD, Professor and Chairman of the Department of Radiology at the University of Nebraska Medical Center, for their incessant support and for providing a positive and a stimulating academic environment.
Shahid M Hussain, MD, PhD Professor of Radiology Director of Body MRI Chief Abdominal Imaging Department of Radiology
University of Nebraska Medical Center 981045 Nebraska Medical Center Omaha, NE 68198 USA
Email: smhussain@unmc.edu
X
How To Use This Book
MR imaging is a unique imaging modality which allows a comprehensive evaluation of the liver and includes the visualization of the soft tissue components based on various T1and T2-weighted sequences, the vascularity based on routine dynamic gadolinium-enhanced imaging and MR angiography, and the biliary tree based on MR cholangiography. The versatility of MR imaging and the amount of the diagnostic information obtained from a single liver MRI examination may intimidate the reader. This book provides a unique approach to simplifying liver MRI.
To diagnose most liver diseases, four sequences are most important to evaluate. These include: (1) a fat-suppressed T2-weighted sequence (or an equivalent sequence); (2) a T1 in-phase gradient-echo sequence; (3) arterial-phase dynamic gadolinium-enhanced images; and (4) delayed-phase gadoliniumenhanced images. This book provides computer-generated drawings of these or four similar MRI sequences to highlight and explain the most important diagnostic findings. The direct MRI drawing comparison facilitates the interpretation of the important imaging findings. In addition, background information and up-to-date available literature is provided, with correlation to other imaging modalities (US, CT) and pathology.
Liver abnormalities are divided into five major categories. Within each category, subcategories are provided and more specific diagnoses are listed alphabetically. Based on this book, liver MRI can be approached as follows:
Step I: Categorize the liver abnormality into one of the five groups:
1.High-fluid content liver lesions (high signal on T2 which persists on longer T2)
2.Solid liver lesions (moderately high signal on T2; similar to the spleen or lower)
3.Diffuse liver lesions (expressed by the diffuse or segmental abnormal signal or enhancement)
4.Vascular liver lesions (visible mainly in the arterial phase)
5.Biliary tree abnormalities (visible on T2-weighted and MRCP sequences)
Step II: Evaluate the signal intensity on fat-suppressed T2and T1-weighted sequences as well as gadolinium-enhanced images and attempt a more specific diagnosis.
Step III: Compare your working diagnosis to the specific examples within each category systematically and confirm your finding into a more definitive (differential) diagnosis.
This approach is consistently applied throughout the book, which shows that most liver lesions can be detected and characterized based on this method. At the end of the book, several examples of differential diagnostic comparisons have been provided of the most common liver lesions. The reader is encouraged to develop a similar approach during reading liver MRI exams in daily clinical practice. In addition, two appendices have been provided to explain a typical liver MR imaging protocol and the normal segmental anatomy of the liver.