For detailed articles on various aspects of liver imaging, please see Radiopaedia search results for liver imaging.
In addition to today’s resource, please review:
How to approach elevated liver enzymes? from the Liver Fellow Network of the American Association For The Study Of Liver Diseases.
Back to Basics: Liver Associated Enzymes from the Liver Fellow Network of the American Association For The Study Of Liver Diseases.
Today, I review, link to, and excerpt from StatPearls‘ “Liver Imaging”. Shahrzad Azizaddini; Nisha Mani. Last Update: February 20, 2023.
All that follows is from the above resource.
- Continuing Education Activity
- Introduction
- Anatomy
- Plain Films
- Computed Tomography
- Magnetic Resonance
- Ultrasonography
- Nuclear Medicine
- Angiography
- Patient Positioning
- Clinical Significance
- Review Questions
- References
Introduction
Liver lesions have a broad spectrum of pathologies, ranging from benign lesions such as hemangiomas to malignant lesions such as primary hepatocellular carcinoma and metastasis. Imaging is a crucial step in diagnosing these conditions, as liver enzymes can be elevated in up to 9% of individuals in the USA.[1][2] A combination of medical history, serologic, and radiologic investigations can provide a diagnosis in most cases.[3] Liver lesions can be categorized into focal and diffuse liver lesions.
Focal liver lesions generally fall into 3 main clinical categories.
Diffuse liver lesions can be categorized into vascular, inflammatory, and storage diseases.
Benign liver lesions can be classified into 3 categories based on their tissue origin:
Liver ultrasonography (US), computed tomography (CT), and magnetic resonance imaging (MRI) are the primary imaging modalities to diagnose liver lesions. Postcontrast imaging can help distinguish lesions depending on their degree of vascularity and composition. Postcontrast hepatic imaging falls into 3 distinct phases: the arterial phase, the portal venous phase, and the delayed venous phase.[4] Ultrasound can be a method of choice as a screening modality, and contrast-enhanced multidetector CT (MDCT) is a modality of choice in most hepatic imaging.[5] MRI plays a role in better-characterizing lesions with equivocal features on US and CT.
Anatomy
The most widely used anatomic classification of hepatic segments is the Couinaud classification,*
Google Search: Couinaud classification
which describes 8 functionally independent liver segments based on vascularization, bile duct distribution, and lymphatic drainage.[6] Each segment is wedge-shaped, with the apex directed towards the hepatic hilum with some variability.[7] A single branch of the hepatic artery, portal vein, and bile duct enters through the apex into the hepatic segments. The hepatic vein runs between 2 adjacent segments and drains into the inferior vena cava (IVC). The middle hepatic vein runs from the inferior vena cava to the gallbladder fossa and divides the liver into the right and left lobes.[8] The right hepatic vein divides the right lobe into the anterior and posterior segments, and the falciform ligament divides the left lobe into medial and lateral segments. The portal vein divides segments horizontally into superior and inferior segments. Segment I is the unique caudate lobe, which can receive dual blood supply from the right and left portal vein and drains directly into IVC. Segments II, III, and IV are left hepatic lobe sections. Segments V, VI, VII, and VIII constitute the right lobe hepatic sections.[9]
The hepatic blood supply is from the portal vein (about two-thirds), and the rest is from the hepatic artery; thus, maximum enhancement of the liver is attained during the portal venous phase, which is 60 to 120 seconds after arterial phase enhancement.[10] Tumors supplied from the hepatic artery enhance during the arterial phase, the principle in transarterial chemoembolization and chemoembolization.[11] Arterial embolization and treatment target tumors rather than normal hepatic cells.[12] The hepatic veins enter the inferior vena cava. They can be seen as anechoic tubes with thin walls on ultrasound (see Image. Color Doppler Ultrasound, Hepatic Veins With Hepatic Venous Waveforms). The portal triad, which includes the portal veins, hepatic arteries, and bile ducts surrounded by fibrofatty tissue, can be seen as echogenic foci throughout the liver.[13]
The portal vein forms from the junction of the superior mesenteric artery and splenic veins behind the neck of the pancreas.[14] Inferior mesenteric, gastric, and cystic veins drain into the portal vein. It divides into the right hepatic vein and porta hepatis. Although the portal vein provides 75% of the liver’s blood supply, it provides 50% of its oxygen supply.[15] Portal hypertension or hepatic venous pressure gradient is a portosystemic pressure gradient. Different pathologies can cause portal hypertension, including portal vein thrombosis, cirrhosis, viral hepatitis, Budd-Chiari syndrome, and congestive heart failure.[16] Ultrasound manifestations of portal hypertension are a dilated portal vein (>13 mm), a dilation of the splenic and superior mesenteric veins, the presence of collateral vessels between the portal and systemic pathways, splenomegaly, ascites, and the presence of biphasic or reversed flow (hepatofugal flow) on Doppler US which is diagnostic and pathognomonic for portal hypertension.[17] Portal hypertension can be appreciated in CT and MRI with similar manifestations on ultrasound and the presence of contrast in the paraumbilical vein, which is pathognomonic.
Hepatomegaly and liver cirrhosis are 2 main pathologies that distort the liver anatomy. Cardiac disease, including congestive heart failure, restrictive cardiomyopathy, and right-sided valvular disease, can cause hepatomegaly and dilation of hepatic veins, called passive hepatic congestion.[18] It is due to hepatic venous drainage impairment and stasis of blood in hepatic parenchyma. Ultrasound manifestations of passive hepatic congestion are right hepatic lobe enlargement, inferior vena cava dilatation, and hepatic vein enlargement.[19] Changes in the hepatic vein and IVC velocity pattern can be appreciated in color Doppler ultrasound with loss of normal triphasic flow and flattening of the waveform in hepatic veins.[20] Congestive right heart failure also can cause painless, diffuse wall thickening of the gallbladder.[21][22] The most common etiologies of cirrhosis are alcohol, followed by viral hepatitis, cryptogenic infection, vascular pathologies, and metabolic disorders.[23] The most common ultrasound changes in cirrhosis are a nodular appearance on the surface, heterogeneous echotexture, relative enlargement of the caudate lobe compared to the right lobe, and atrophy of the medial segment of the left lobe. The presence of portal hypertension imaging changes increases the sensitivity and specificity of cirrhosis based on the ultrasound changes, but these usually happen in the advanced and late stages of cirrhosis.[3]
Plain Films
Plain films are rarely helpful in assessing hepatic pathology except for evaluating hepatomegaly when the liver shadow extends beyond the shadow of the right kidney.
Computed Tomography
CT imaging of the liver can be done with different protocols, including unenhanced, single-phase, dual-phase, and triphasic contrast-enhanced protocols.[24] Each of these liver CT protocols is important in evaluating different liver pathologies. The single-phase contrast-enhanced CT is generally the modality of choice in the portal venous phase in CT, which is typically 70 seconds after intravenous (IV) contrast injection, and the liver has the maximum enhancement. It can mainly provide information about diffuse liver pathologies, such as liver cirrhosis and hypovascular metastatic liver disease. The dual-phase contrast-enhanced CT is the primary imaging modality conducted in the portal venous and late arterial phases, which can be obtained approximately 35 seconds after IV injection and might provide better information about hypervascular lesions.[25]
This protocol can help with hypervascular metastatic lesions like renal cell carcinoma, breast cancer, melanoma, and endocrine tumors and preoperative evaluation for partial hepatic resection. It can provide the referring surgeon with information about liver anatomy and vasculature. Triphasic contrast-enhanced CT constitutes non-enhanced arterial and portal venous or arterial, venous, and delayed phases.[26] Arterial phase enhancement begins approximately 20 to 25 seconds after IV contrast injection. Hypervascular pathologies, like most benign and malignant hepatic lesions, can be appreciated in this phase. Triphasic protocols usually are used in patients with possible cirrhosis and hepatocellular carcinoma (HCC).[27] HCC is a hypervascular lesion that enhances during the arterial phase and has a fast wash-out during the portal venous phase.[28] Cholangiocarcinoma is 1 of the liver pathologies that can be appreciated better on a triphasic CT technique, with non-enhanced, portal venous phase and delayed phase (10 to 15 minutes) hyperenhancement due to fibrous tissue.[29] See Image. Cholangiocarcinoma.
Fatty liver disease is a common condition that can present with different patterns. Because of its important clinical consequences in the long term, radiologists should provide detailed descriptions of fatty changes. The 6 main important patterns of fatty liver infiltrations are diffuse, focal, geographic, subcapsular, multifocal, and perivascular. Fatty liver changes are hyperechoic lesions compared to the spleen and renal cortex.[30] Hepatic steatosis, either diffuse or focal, is best evaluated on a non-contrast CT of the abdomen. In a non-contrast study, the liver measures at least 10 Hounsfield units (HU) less than the spleen in hepatic steatosis.[31] On a contrast-enhanced CT scan, the liver and spleen have different rates of contrast uptake. In the portal venous phase, a hepatic attenuation of 25 HU less than the spleen suggests steatosis.[32] Fatty liver disease on MRI can be appreciated by the signal drop in gradient-echo T1-weighted out-of-phase images compared to in-phase.[33]
Diffuse fatty liver is the most common form of liver steatosis. Diffuse steatosis with hepatomegaly and increased caudate-to-right lobe ratio increase the possibility of non-alcoholic steatohepatitis (NASH).[34] Focal hepatic steatosis can have similar imaging features as specific benign and malignant liver lesions, and MRI can help differentiate different entities. Areas in the liver that are more susceptible to focal hepatic steatosis are perivascular and subcapsular regions adjacent to the hepatic hilum or falciform ligament, which are the same areas for focal hepatic sparing in the diffuse fatty infiltration as a result of altered intrahepatic blood flow with aberrant venous system and no portal inflow.[35]
Geographic fatty liver disease can occur secondary to some parenchymal disease like cholangitis, or involvement of the right liver lobe can be related to the feeding of this part of the liver by the superior mesenteric vein, which has lipogenic materials from gastrointestinal tracts. Subcapsular fat deposition can be visible in insulin-dependent diabetes patients due to fat accumulation in the subcapsular region secondary to higher insulin concentration.[36] Multifocal fat deposition can resemble metastasis, abscesses, lymphoma, sarcoidosis, and hemangiomatosis in the ultrasound and CT, but MRI can differentiate the presence of fat with the signal drop in out-of-phase images.[37] Fat deposition around the portal vein or hepatic vein can have similar ultrasound and CT imaging characteristic features as Budd-Chiari syndrome, periportal edema, and MRI can differentiate fat deposition from other pathologies.
Non-contrast CT can be useful for evaluating and detecting iron and calcium deposition in the liver. Amyloidosis and Wilson disease mainly have nonspecific liver imaging features. Amyloidosis, abnormal deposition of amyloid fibrils, can have a nonspecific liver imaging manifestation like diffuse hepatomegaly, diffuse or focal areas of hypoattenuation, heterogeneous appearance, or periportal involvement.[38] Wilson disease is an autosomal recessive disorder that causes the accumulation of copper in different organs, such as the basal ganglia, cornea, and liver. The CT manifestation of Wilson disease in the liver can be nodular areas of hyperattenuation due to fatty infiltration and copper accumulation in the liver.[39]
The presence of gas in the portal vein can have various etiologies, and it should be differentiated from pneumobilia. Portal venous gas is peripheral in location, while pneumobilia is central.[40] It manifests as echogenic foci in the portal vein lumen in the ultrasound and foci of low density in the liver, portal vein, and its branches in CT. Pneumobillia is the presence of gas in the biliary tree, which is more central. Portal venous gas can be caused by umbilical vein catheterization, necrotizing enterocolitis, or postoperative findings in corrective bowel surgery in children. It can be related to ischemic bowel, inflammatory bowel disease, upper and lower endoscopic procedures, and intra-abdominal sepsis in adults.[41] Pneumobillia can be seen in the setting of recent biliary instrumentation, an incompetent sphincter of Oddi, biliary-enteric surgical anastomosis, and spontaneous biliary-enteric fistula.[42]
The hepatic abscess, often a cystic-appearing lesion, usually arises from an infectious process in the gastrointestinal system that carries the infection to the liver via the portal venous system. Escherichia coli is the most common microorganism.[43] The imaging characteristic of a hepatic abscess is a double target sign, a central area of low attenuation surrounded by 2 layers of rings.[44] The inner layer can appear as a high attenuation rim, with early and persistent delayed contrast enhancement, and the outer layer enhances only in the delayed phase. Hepatic abscess imaging features on T2-weighted MRI can demonstrate an irregular wall with late enhancement and central area of T2 hyperintensity.[45] Due to disseminated candidiasis, fungemia is another infection process that can occur in immunocompromised patients. Liver and spleen involvement is visible in CT as multiple small hypoattenuating lesions, which may have ring-enhancing and look like microabscesses. Although MRI has better sensitivity and specificity, CT has been used more frequently because it is less expensive and more accessible.[46]
Magnetic Resonance
MRI has advantages and disadvantages compared to ultrasound and CT. Lack of ionizing radiation, higher cross-sectional resolution, presence of extracellular and hepatocyte-specific contrast agents, and the ability to give better and more accurate information about the diffuse liver lesion and characterization of focal liver lesions make MRI the best imaging modality in liver imaging. However, it costs more, takes longer to acquire images, and requires patient cooperation, such as breath-holding, to have better and fewer motion artifacts (see Image. Aliasing Artifact).[47]
The liver MRI protocol consists of multiple sequences before and post-contrast. Post-contrast phases include the arterial phase, portal venous phase, equilibrium phase, hepatobiliary delayed phase, and later delayed phase.[48] Hepatobiliary-specific contrast agents that are used in liver MRI are mangafodipir trisodium (Mn-DPDP), gadobenate dimeglumine (Gd-BOPTA), and gadoxetic acid (Gd-EOB-DTPA). These contrast agents have specific characteristics such as specific receptors and transporters for uptake, different excretion percentages via the biliary and renal systems, method of administration, and side effects. These hepatocyte-specific contrasts can better help identify and characterize small liver lesions, especially well-differentiated HCC. It can be used to distinguish FNH from hepatic adenoma. Hepatic adenoma is visible in the hepatobiliary phase as a hypointense lesion versus FNH that is iso or hyperintense when evaluating hepatic disease during HCC surveillance and post-liver transplant evaluation. It can also differentiate tumors with a hepatocellular origin from nonhepatocellular ones.[49] Contrast agents secreted into bile can differentiate hepatocellular adenoma (HCA) by early heterogeneous enhancement in T1-weighted fat-suppressed arterial phase MRI and subsequent contrast washout in the portal venous phase. Because HCA has no bile ducts, uptake of biliary-specific contrast is minimal in the delayed phase.[50]
The most sensitive imaging technique to assess the presence and degree of hepatic steatosis is in and out gradient recalled echo (GRE) MRI. However, a liver biopsy is the gold standard method to evaluate the presence of inflammatory and early fibrotic changes.[50] Magnetic resonance elastography is a newer technique introduced originally as ultrasound elastography, which can measure liver stiffness and degree of fibrosis.[51] Magnetic resonance elastography does not have the possible sampling bias in liver biopsy. It has better sensitivity and specificity compared to ultrasound elastography, which has limitations in obese patients and patients with ascites. Iron overload and accumulation in hepatic and hepatic Kupffer cells can occur in hemochromatosis and hemosiderosis. The liver is the primary organ of deposition and can present as hepatomegaly as the first sign of disease.[52] It can be seen as hypointense compared to paraspinal muscle signal in T1 and T2 Weighted and GRE T2 weighting MRI.[53]
Hepatic hemangioma is the most common benign liver lesion that can be categorized into typical and atypical hemangiomas. A typical hepatic hemangioma can be appreciated on non-contrast CT as a hypo-attenuating lesion most of the time. In arterial phase contrast-enhanced CT, these neoplasms present as a lesion with nodular enhancement in the periphery. Portal venous and delayed phases show continuous enhancement of the periphery with contrast filling the central part.[54] Hemangioma is hypointense on T1 imaging and hyperintense on T2 imaging. Gadolinium-enhanced contrast T1 imaging often shows nodular enhancement of the periphery with a progressive enhancement of the central part and retaining the contrast in delayed imaging. Hepatobiliary contrast T1 imaging is non-specific and may not be helpful. Two main categories for atypical hemangiomas are giant hepatic hemangiomas and flash-filling hepatic hemangiomas. Giant hemangiomas are remarkably large but non-neoplastic vascular lesions with radiologic manifestations similar to hepatic hemangiomas.[55] Flash-filling hepatic hemangiomas/venous malformations are smaller (mostly less than 2 cm) and have a hyperechoic appearance in the ultrasound.[56] They are hypo- or iso-dense in noncontract imaging and demonstrate a fast and homogenous enhancement in the arterial phase while retaining the contrast in the late phase. Flash-filling hemangiomas have similar imaging manifestations in CEUS and gadolinium-enhanced contrast MRI with quick, homogenous enhancement and no washout in the late phase.
Focal nodular hyperplasia (FNH) is the second most common benign liver mass with a hepatocellular origin. It has a central scar with fat and fibrous tissue contents and an increased density of hepatocytes in about 80% of FNH.[57] MRI has better sensitivity and specificity in diagnosing FNH than CT and ultrasound. FNH consists of hepatocytes, bile ducts, and Kupffer cells in an abnormal alignment. The ultrasound appearance of FNH includes subtle changes in the liver contour or parenchymal echogenicity.[57] FNH is iso- or hypointense in nonenhanced T1 imaging and has a homogenous enhancement on the arterial phase. FNH can be appreciated in multiphasic MRI with hyperintense and delayed enhancement in T2 weighted images due to retaining contrast in hepatocytes because of a central scar.[57]
Hepatic adenomas are rare and benign liver tumors with a hepatocellular origin, most commonly related to long-term oral contraceptive use.[58] Other factors precipitating hepatic adenomas are anabolic steroids, glycogen storage diseases, obesity, and metabolic syndrome.[59] Although hepatic adenomas are benign liver tumors, they have a potential risk of bleeding and malignant degeneration.[60] Surgical resection is the recommended treatment for hepatic adenomas. For patients in which resection is not feasible or not preferable, modifying risk factors, serial imaging, and monitoring alpha-fetoprotein levels are possible management options. Hepatic arterial embolization can be considered in select cases.[61]
A hepatic cyst is a common hepatic lesion with a cholangiocellular origin. Benign hepatic cyst(s) can be found in around 5% of the general population.[62] Its size can vary from microscopic to sometimes greater than 20 cm in diameter.[63] Ultrasound can characterize hepatic cysts as anechoic lesions with thin walls and the presence of posterior acoustic enhancement, which confirms the fluid content of the cyst and very thin septa in some cases. CT imaging can be appreciated as an area of low internal attenuation with a thin wall and the possible presence of thin septa. Cysts can be appreciated in the MRI as an area of homogenous low signal in T1-weighted imaging, homogenous high internal signal in T2-weighted imaging, and absence of enhancement with contrast.[64] See Image. Hepatic Cysts.
Hepatocellular carcinoma (HCC) is the most common primary liver tumor. Cirrhosis and chronic hepatitis are the major risk factors for the development of HCC. Alpha-fetoprotein becomes elevated in two-thirds of HCC. Elevated alpha-fetoprotein in the presence of cirrhosis is suggestive of HCC and can be seen in 70% of patients with HCC.[65][66] HCC can appear on ultrasound from focal hypoechoic, hyperechoic, and heterogeneous lesions. Most HCCs are hypervascular on color Doppler. In contrast-enhanced ultrasound, HCC can be appreciated with enhancement in the arterial phase and washout on the portal venous phase.[67] MRI and CT have 82% and 56% sensitivity in detecting HCC, respectively.[68][69] In CT, the enhancement pattern is similar to contrast-enhanced ultrasound. Because of the possible arterioportal shunt in HCC, focal fatty changes might be seen as focal fat deposition in the normal liver or focal fat sparing around the HCC in diffuse hepatic steatosis. HCC results from a regenerative nodule’s progression to dysplastic nodules and high-grade dysplastic nodules to low-grade HCC. The portal vein feeds regenerative and dysplastic nodules, which are indistinguishable from each other on imaging, although dysplastic nodules are premalignant, and regenerative nodules are not. Most regenerative and dysplastic nodules are hypo-intense in T2- T2-weighted images and have variable intensity in T1- T1-weighted images. Regenerative nodules and low-grade dysplastic nodules are isointense in contrast-enhanced MRI.[70] [71]
Hepatocellular carcinoma (HCC) receives blood from the hepatic artery compared to healthy hepatic tissue that gets supply from the portal vein. Because of this characteristic, HCC can be appreciated in multiphasic, contrast-enhanced MRI by increasing contrast enhancement in the arterial phase and contrast washout in the portal phase with peripheral rim enhancement. HCC appears slightly hyperintense T2-weighted unenhanced MRI. The hepatic artery and portal vein feed cholangiocarcinoma, so there is an increasing contrast enhancement in both arterial and venous phases.[50][70]
Fibrolamellar carcinoma is a subtype of HCC and has a better prognosis than the typical HCC. These generally occur in younger patients and do not demonstrate elevated alpha-fetoprotein levels. Fibrolamellar HCC on imaging is usually large at diagnosis and does not have a capsule. Fibrolamellar carcinoma appears on T1- and T2-weighted MRI as a large, heterogeneous mass with central hypointensity due to central fibrotic scar.[72]
Metastatic liver lesions are usually hypointense on T1-weighted imaging and hyperintense on T2-weighted images. Most metastatic liver tumors are hypovascular, and the portal venous phase is the phase for visualization. Some metastatic tumors, including renal cell carcinoma, melanoma, and sarcoma, are hypervascular. These liver metastases can be appreciated best in the arterial phase.[73]
Ultrasonography
Ultrasonography is often the first imaging modality in evaluating and screening for focal and diffuse liver pathologies due to its availability, low cost, and noninvasive.[74] Liver pathology on ultrasound can present with different patterns such as generalized hypoechogenicity, as seen in acute hepatitis and diffuse malignant lesions, generalized hyperechogenicity, as seen in diffuse hepatic steatosis, and anechoic/hyperechoic lesions as seen in various benign and malignant lesions. Benign hyperechoic lesions include hemangioma, hepatic adenoma, focal nodular hyperplasia, and focal fatty changes. Malignant hyperechoic lesions include hepatic metastases from colorectal, renal cell carcinoma, melanoma, cholangiocarcinoma, and HCC.[75] Ultrasonography has limitations, including interobserver variability and decreased accuracy in patients with large body habitus.[49]
Ultrasonography, in combination with techniques and tools, has a significant role in diagnosing and treating different liver pathologies, for example:
A cirrhotic liver can appear hyperechoic on ultrasound. The sensitivity of diagnosing cirrhosis by ultrasound can vary and be as high as 91%.[84] The presence of signs and symptoms of portal hypertension, such as increased spleen or portal vein diameter, can increase the sensitivity of ultrasound in later stages of cirrhosis.[3] A hypervascular nodule in CEUS has a higher specificity for small HCC, less than 2 cm, than CT and MRI studies. Liver metastasis appearance mainly depends on the primary source of the tumor. It can appear as hypoechoic or hyperechoic lesions. The presence of a hyperechoic halo sign is suggestive of a malignant lesion.[85] In CEUS, metastasis has variable echogenicity in the arterial phase, but the washout appearance on the portal phase can help detect malignant lesions.[86]
One of the important applications of the Doppler ultrasound is in post-transplant patients. Hepatic arterial thrombosis is the most common vascular complication after a liver transplant. The resistive index (RI) is a Doppler parameter to evaluate it, measured by subtraction of peak systolic velocity from end-diastolic velocity, divided by peak systolic velocity.[87] The RI normal range is between 0.55 to 0.8. Low RI is more specific in patients with a liver transplant, which can be related to partial arterial obstruction in the proximal part of the artery, peripheral vascular shunts, and portal hypertension. In comparison, high RI can be related to microvascular compression, disease, or physiologic.[88]
Hemangioma is the most common benign liver lesion. It is usually an incidental finding in asymptomatic patients as the most common hyperechoic liver lesion.[54] It can appear on ultrasound as a hyperechoic lesion with a distinct border and peripheral feeding vessel on color Doppler.[56][89] A hemangioma appears in the arterial phase of CEUS with peripheral nodular enhancement, portal venous phase, and late phase with continuous contrast filling and changing to a hyperechoic lesion. In asymptomatic patients without any history of malignancy, diagnosis of hemangioma can be made solely based on imaging manifestation of a single, well-defined, homogenously hyperechoic lesion in the ultrasound; no further workup is necessary.[90]
The imaging manifestation of viral hepatitis in ultrasound can range from normal to nonspecific findings of hepatomegaly, gallbladder wall thickening, fluid accumulation around the portal vein, or generalized hypoechogenicity.[91] The diagnosis is mainly made based on clinical features and serology testing.
Nuclear Medicine
Positron emission tomography (PET) and single-photon emission computed tomography (SPECT) are the nuclear imaging techniques used more frequently to diagnose liver malignancy and evaluate response to treatment metastasis, recurrence, and prognosis. F-fluorodeoxyglucose (FDG)-PET and C-acetate PET are more common nuclear imaging modalities in diagnosing liver malignancy.[92] Although it has high sensitivity, the false positive rate is high due to detecting any focal hypermetabolism area. The sensitivity is low in the detection of lesions smaller than 1 cm. Transarterial radioembolization and selective internal radiotherapy are theragnosis methods in the nuclear medicine field, and PET or SPECT is used simultaneously for diagnosis and treatment.[93]
Angiography
Multidetector computed tomography angiography (MDCT) is an imaging method to assess liver neoplasm for staging and surgical planning by providing information about hepatic vascular anatomy and parenchymal pathology. Biphasic hepatic CT with arterial and portal venous phases can appreciate hypervascular tumors with increased sensitivity than the portal phase alone. MDCT angiography has been the imaging modality of choice for living donor liver transplantation and evaluating any arterial complications after the transplant.[94]
Transarterial chemoembolization therapy (TACE) is a method in which chemotherapy is administered directly into the hepatic artery, feeding the tumor and resulting in necrosis. Its primary use is treating HCC and specific liver metastasis, such as colorectal metastases and cholangiocarcinoma. It can also be useful for unresectable HCC.[95]
Patient Positioning
Ultrasound is the main liver imaging technique, and patient positioning and operator expertise are important factors in optimizing the study.[96]
Clinical Significance
The first imaging modality to evaluate liver pathology depends on the patient’s clinical situation, the availability of different modalities, the technician’s familiarity with the test, and the physician’s familiarity with the test. Ultrasound and CT remain the first imaging modality to assess the diffuse and focal liver lesion for screening and characterization. Based on the findings of ultrasound and CT, further workup and imaging can occur.
Hepatic steatosis or fatty liver is the most common abnormal imaging finding in liver imaging, which can be related to alcoholic liver disease and nonalcoholic liver disease, including obesity, insulin resistance, diabetes, hyperlipidemia, and hypertension. Nonalcoholic fatty liver disease can progress from simple fatty liver disease to nonalcoholic steatohepatitis (NASH) and cirrhosis. Regardless of etiology, ultrasound findings of fatty liver disease include increased echogenicity of the liver compared to the renal cortex, loss of normal echogenicity of the portal triad in the periphery of the liver, and poor visualization of the diaphragm. Transient elastography is the most validated technique with more sensitivity and specificity (87% and 91%, respectively) in diagnosing cirrhosis than diagnosing significant fibrosis (70% and 84%, respectively).[97]
Risk stratification is essential in patients with liver cirrhosis to estimate complications risks such as portal hypertension consequences and liver cancer. Liver serology and elastography are noninvasive methods to determine patients with advanced liver cirrhosis. A liver biopsy can provide information about the stages of fibrosis. Elastography is a method that can show the increased stiffness of the parenchyma. Among the different approaches to elastography, vibration-controlled transient elastography is the most common type used worldwide.[3]
Liver Imaging Reporting and Data System (LI-RADS)* is a comprehensive and standardized system for reporting and classifying liver lesions at an increased risk of developing into HCC.[98] LIRAD categorizes lesions into definitely benign, probably benign, probably or malignant, but not HCC specific, intermediate probability of malignancy, probably HCC, and HCC. It guides radiologists, clinicians, and surgeons for surveillance guidelines and recommendations if a biopsy is necessary.
LI-RADS®
Liver Imaging Reporting and Data System from American College Of Radiology
