Focal Liver Lesions MRI

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    Focal liver lesions

    MR imaging

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    MRI TechniquesSequences

    Coronal ultrafast spin-echo sequence(single breath-hold).

    Axial fast spin-echo (T2-weighted)images.

    Fat-saturated (frequency selective)

    images increase the conspicuity ofliver lesions.

    Axial 2D dual spoiled gradient-

    recalled echo sequence (SPGR) (bothout-of- hase and in hase ima in

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    Sequences

    T1-weighted imaging

    Diffusion-weighted imaging.

    Dynamic contrast materialenhancedimaging at 20 (arterial phase), 60(portal venous phase), and 120

    (equilibrium phase) seconds after theinjection of Gd-BOPTA and again at 1hour after injection

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    Contrast agents

    Extracellular fluid agents.

    Hepatobiliary-specific agents.

    Combined agents. Reticuloendothelial agents,

    Blood-pool agents

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    Hepatobiliary-specific Agents(Gd-BOPTA)

    These hepatobiliary-specific agentsare taken up to varying degrees byfunctioning hepatocytes and are

    excreted in the bile.

    Gadolinium-based hepatobiliary-specific agents initially distribute in

    the extracellular fluid compartment,just as extracellular fluid agents do,and are subsequently taken up by

    hepatocytes.

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    Focal liver lesions in MRI

    Classification based on vascularizationpatterns

    1.

    Hypervascular lesions.2. Hypovascular lesions.

    3. Lesions presenting delayed

    persistent enhancement.

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    Hypervascular lesions

    Characterized by strong contrastenhancement in the arterial phasescan.

    May be sharply demarcated or morediffuse appearance.

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    Hemangioma

    well-circumscribed mass of blood-filled spaces lined by endothelium ona thin fibrous stroma.

    On T2-weighted images, they aremarkedly hyperintense and havecystlike signal intensity.

    On T1-weighted images, hypointenserelative to the liver.

    Three distinct enhancement patterns:

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    Capillary Hemangioma

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    Focal Nodular Hyperplasia

    Represent a hyperplastic response ofthe hepatic parenchyma to apreexisting arterial malformation.

    After hemangiomas, most incidentalhypervascular liver lesions innoncirrhotic livers represent FNH and

    not adenoma. FNH - margin of the lesion, is

    typically ill-defined or lobulated.

    Adenomas - mar in is usuall smooth

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    T1-weighted images - isointenserelative to the liver

    T2-weighted images - isointense toslightly hyperintense.

    Central scar is T1 hypointense and

    T2 hyperintense.

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    Hepatic Adenoma

    Hepatic adenoma is a very rarebenign neoplasm.

    Multiple in about 20% of cases,especially in patients with glycogenstorage disease.

    Composed of benign hepatocytesthat are arranged in large plates orcords without acinar architecture.

    T1-weighted images - variable signalintensit .

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    Hepatic adenoma

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    HepatocellularCarcinoma

    Cirrhotic nodules range frombenign regenerative topremalignant dysplastic and frankly

    malignant HCC. T1-weighted MR imaging, HCC

    lesions less than 1.5 cm are often

    isointense, whereas larger lesionsmay be hyperintense secondary tolipid, copper, or glycogen.

    Fatty metamorphosis in a cirrhotic

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    HepatocellularCarcinoma

    In cirrhotic patients, a hypervascularmass with increased T2 signal similarto that of the spleen is suspicious for

    HCC. DWI - Well-differentiated tumors are

    often isointense, whereas moderately

    to poorly differentiated tumors aremore often hyperintense.

    Arterial phase -heterogeneous

    enhancement, portal venous and

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    HepatocellularCarcinoma

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    HypervascularMetastases

    Hypovascular metastases showdecreased enhancement relative tonormal liver and are most

    conspicuous on portal venous phaseimages.

    Hypervascular metastases enhance

    earlier, are best seen on arterialphase images, and show washout ondelayed images.

    These metastases typically arise

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    Hypervascular lesions -arterial phase

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    Hypervascular lesions -arterial phase

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    Hypovascular lesions

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    Delayed persistentenhancement

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