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Lesions in the liver are often characterized based upon underlying histology. The most common benign lesions include simple cysts, hemangiomas, hepatocellular adenoma (HCA), focal nodular hyperplasia (FNH), regenerative nodules, and hepatic abscess.
Most benign hepatic lesions are asymptomatic and found incidentally ( Fig. 17.1 ). Symptoms, if present, are often related to mass effect including pain/discomfort, nausea, vomiting, or early satiety.
Hepatic abscess may present with signs of infection including fever and leukocytosis.
HCA can present with hemorrhage and possible rupture.
Multiphase computed tomography (CT) including hepatic arterial phase, portal venous phase, and delayed phase (equilibrium, 3 min) is the protocol of choice for evaluation of hepatic lesions.
Precontrast acquisition may be helpful in evaluation of cysts and areas of spontaneous hyperdensity.
In- and out-of-phase imaging and fat suppression techniques can demonstrate areas of microscopic and macroscopic fat, respectively.
Hepatocyte specific contrast agents are taken up by well differentiated/functional hepatocytes, which allows for evaluation for dedifferentiated masses or masses of nonhepatic origin using uptake characteristics. Commonly used agents include Eovist/Primovist (Gd-EOB-DTPA; 50% hepatocyte uptake) and MultiHance (Gd-BOPTA; 2%–4% hepatocyte uptake) ( Fig. 17.2 ).
Diffusion-weighted imaging (DWI) can evaluate impedance to the microscopic movement of water molecules often indicating areas of increased or disorganized cellularity.
Low cost, lack of ionizing radiation, and availability make ultrasound (US) a good modality for primary evaluation.
Decreased sensitivity because of body habitus and bowel gas, operator skill dependence, and limited field of view are all limitations to this modality.
Although some lesions, such as cysts (anechoic) and hemangiomas (hyperechoic) are often easily identified, others may be indistinguishable from background liver.
Elastography and microbubble contrast may provide additional diagnostic information.
Often incidental and asymptomatic, they are most common in middle aged women (5:1), although cysts can be seen at any age and may demonstrate mass effect if large enough.
They be complicated by hemorrhage, rupture, or secondary infection.
Lined by cuboid epithelium identical to bile ducts, indicating biliary origin.
May cause increased alkaline phosphatase or bilirubin if there is mass effect upon the bile ducts.
Cysts are thin walled well-defined fluid attenuating lesions that are often unilocular although septae or multiloculation may be present. Neither the cyst nor wall should show enhancement ( Fig. 17.3 ).
Prolongation of both T1 and T2 because of fluid content is present, which manifests as low T1 signal and high T2 signal. Internal hemorrhage may show variable signal intensities based upon age and amount of blood content. No enhancement or connection to the biliary tree should be present.
Well-defined anechoic lesion with posterior acoustic enhancement and no internal flow on Doppler.
Complex features or deviation from the aforementioned imaging characteristics should make one consider alternative diagnoses ( Fig. 17.4 ). These include abscess, hydatid cysts, peribiliary cysts ( Fig. 17.5 ), biliary hamartoma/cystadenoma/cystadenocarcinoma ( Figs. 17.6 and 17.7 ), choledochal cyst ( Fig. 17.8 ), or necrotic metastases.
Polycystic kidney disease, Von Hippel Lindau.
Conservative. Percutaneous drainage, sclerosis, or laparoscopic fenestration may be considered if symptomatic.
Most common benign hepatic lesion and more common in middle aged women.
Kasabach-Merritt syndrome can manifest with consumptive coagulopathy and thrombocytopenia in the setting of giant hemangiomas.
Decreased incidence and size is noted in cirrhotic livers.
Most often hypoattenuating on precontrast imaging although may be iso- or hyperattenuating in a fatty liver. Calcifications may be present in giant hemangiomas. Arterial peripheral discontinuous nodular enhancement with progressive centripetal filling on portal and delayed phase imaging is the classic presentation ( Fig. 17.9 ). Flash filling (capillary) hemangiomas may show rapid complete enhancement on arterial phase.
Long T1 and T2 values manifesting as low T1 signal and high T2 signal are common. Enhancement characteristics are similar to CT. There is often less uptake of hepatocyte specific agents, such as Gd-EOB-DTPA in comparison to the surrounding parenchyma. T2 weighted acquisitions may show low signal internal fibrous bands.
Typical presentation is a homogenous hyperechoic mass. Less than 10% may be hypoechoic with a hyperechoic rim.
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