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Page 8 of 16                                        Brunsing et al. Hepatoma Res 2020;6:59  I  http://dx.doi.org/10.20517/2394-5079.2020.50
















               Figure 4. Positive dynamic-AMRI examination: 80-year-old male with HCV cirrhosis, images show a 11 mm observation in segment 7.
               The lesion has major features of HCC including nonrim APHE, washout and enhancing capsule (arrows) indicating definite HCC (LI-
               RADS-5). AMRI: abbreviated magnetic resonance imaging; HCV: hepatitis C virus; HCC: hepatocellular carcinoma; LI-RADS: Liver
               Imaging Reporting and Data System; APHE: arterial phase hyperenhancement

               Advantages
               Dynamic-AMRI offers unique advantages. The defining imaging features of HCC (i.e., the LI-RADS major
               features of size, APHE, washout appearance, and enhancing capsule appearance) are determined from
               dynamic imaging. When a liver observation meets the required diagnostic criteria, dynamic AMRI alone
               suffices for definitive diagnosis of HCC per LI-RADS (i.e., LR-5). It also permits the diagnosis of tumor
               in vein (TIV). Additionally, it provides cost benefits, as the contrast agents used in dynamic AMRI are
                                                                                                  [52]
               typically less expensive than the contrast agent (gadoxetate disodium) required for HBP-AMRI . Some
               investigators have used coronal T2 imaging for localizer sequences, which can aid in characterizing benign
               lesions such as simple cysts and hemangiomas.

               Disadvantages
               The disadvantages of dynamic-AMRI relate to the lack of additional non-contrast sequences, which may
                                                                                         [53]
               provide ancillary imaging features otherwise not available from the dynamic images . The inability of
               dynamic-AMRI to evaluate these features may cause miscategorization of observations. In particular,
               dynamic-AMRI might over-categorize some vascular pseudolesions (e.g., arterio-portal shunts) as
               indeterminate (LR-3), potentially leading to unnecessarily close follow up. In theory, dynamic-AMRI
               also might under-categorize some early or small HCCs as LR-3, potentially delaying diagnosis, but the
               frequency with which this occurs is thought to be low. HCC detection by dynamic-AMRI depends on the
               timing and quality of arterial-phase imaging, which cannot be repeated if these images are mistimed or
               degraded by motion artifact or other problems. Finally, dynamic-AMRI requires a power injector for bolus
               intravenous administration of GBCA, which may not be available at all facilities and introduces complexity.

               Studies to date
               A few studies to date have retrospectively assessed the performance of a simulated dynamic-AMRI (derived
               by extracting only the dynamic sequences from a complete MRI) for HCC detection in patients with
               cirrhosis [Table 2]. These studies have shown that dynamic AMRI is diagnostically similar to complete MRI
               for HCC detection [26,27] , with per-patient reported sensitivity and specificity of 94% and 88%, respectively .
                                                                                                       [26]
               However, these studies were conducted in diagnostic cohorts, in whom complete MRIs were indicated for
               known or clinically suspected liver lesions, which may have caused inflation in the sensitivity estimates.
               Dynamic-AMRI has yet to be tested prospectively in an HCC surveillance population.


               Summary Statement
               Dynamic-AMRI can characterize the defining imaging features of HCC and allows the detection and
               diagnosis of HCCs in a single surveillance exam. The absence of T2 weighted and DWI sequences, however,
               may cause diagnostic uncertainty, particularly for benign vascular pseudolesions, and lead to unnecessary
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