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Hepatic MRI Using the Double-Echo Chemical Shift Phase-Selective Gradient-Echo Technique

Jeong-Sik Yu1, Jun-Gyun Park1, Eun-Kee Jeong1,2, Mi-Suk Park1 and Ki Whang Kim1

1 Department of Radiology and Research Institute of Radiological Science, Yonsei University College of Medicine, YongDong Severance Hospital, 146-92 Dogok-Dong, Gangnam-Gu, Seoul 135-720, South Korea.
2 Present address: Department of Radiology, Utah Center for Advanced Imaging Research, University of Utah, Salt Lake City, UT 84108.


Figure 1
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Fig. 1A 43-year-old man with diffuse and geographic hepatic steatosis. Signal of hepatic parenchyma is homogeneous on transverse in-phase spoiled gradient-echo MR image (TR/TE, 140/5.3; flip angle, 90°).

 

Figure 2
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Fig. 1B 43-year-old man with diffuse and geographic hepatic steatosis. Out-of-phase image (TE, 2.7 msec) corresponding to A shows signal loss from hepatic parenchyma with geographic pattern.

 

Figure 3
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Fig. 1C 43-year-old man with diffuse and geographic hepatic steatosis. Subtracted image of out of phase (B) from in phase (A) shows high signal intensities of fatty deposition that correspond to the findings in A and B and that can be distinguished from dark signal fat-spared areas (arrowheads).

 

Figure 4
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Fig. 2A 36-year-old woman with diffuse hepatic steatosis and metastases from pancreatic cancer. Transverse in-phase spoiled gradient-echo MR image (TR/TE, 140/5.3; flip angle, 90°) shows multifocal hypointense lesions (arrows).

 

Figure 5
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Fig. 2B 36-year-old woman with diffuse hepatic steatosis and metastases from pancreatic cancer. Out-of-phase image (TE, 2.7 msec) shows perilesional hyperintense rims (arrowheads) distinguished from decreased signal of background fatty liver.

 

Figure 6
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Fig. 2C 36-year-old woman with diffuse hepatic steatosis and metastases from pancreatic cancer. Areas (arrowheads) of dark signal on subtracted image of out of phase (B) from in phase (A) imaging includes lesions and perilesional fat-spared areas. Decreased portal venous perfusion around metastases prevented perilesional fat deposition.

 

Figure 7
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Fig. 3A 50-year-old man with cirrhosis from chronic hepatitis B virus and dysplastic nodule containing intracellular fat. Transverse out-of-phase image (TR/TE, 140/2.7) shows small hypointense nodule (arrow) in left lobe of liver. Corresponding in-phase image (not shown) (TE, 5.3 msec) showed relatively high-signal-intensity nodule at same site.

 

Figure 8
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Fig. 3B 50-year-old man with cirrhosis from chronic hepatitis B virus and dysplastic nodule containing intracellular fat. Nodular hyperintensity (arrow) on subtracted image of out of phase from in phase suggests presence of fatty component within lesion.

 

Figure 9
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Fig. 4A 55-year-old woman with cirrhosis from chronic hepatitis B virus and small hepatocellular carcinoma containing small amount of fat. Transverse in-phase spoiled gradient-echo MR image (TR/TE, 140/5.3 msec; flip angle, 90°) shows hypointense nodule (arrow). Out-of-phase image (not shown) (TE, 2.7 msec) also showed hypointensity for same nodular lesion.

 

Figure 10
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Fig. 4B 55-year-old woman with cirrhosis from chronic hepatitis B virus and small hepatocellular carcinoma containing small amount of fat. Hyperintense area (arrow) on subtracted image of out of phase from in phase suggests intralesional fatty content, which was difficult to identify by direct comparison of in-phase and out-of-phase images.

 

Figure 11
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Fig. 4C 55-year-old woman with cirrhosis from chronic hepatitis B virus and small hepatocellular carcinoma containing small amount of fat. Transverse in-phase dynamic MR image during arterial phase shows lesional enhancement (arrow) of hypervascular tumor.

 

Figure 12
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Fig. 5A 50-year-old man with cirrhosis and hepatocellular carcinoma treated by transarterial chemoembolization 3 months earlier. Transverse in-phase spoiled gradient-echo MR image (TR/TE, 140/5.3; flip angle, 90°) shows hyperintense nodule (arrow). Profound signal loss was observed on out-of-phase images (not shown), and subtracted images (not shown) showed hyperintensity for same lesion due to lipid content of intralesional iodized oil mixed with necrotic tissue after chemoembolization.

 

Figure 13
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Fig. 5B 50-year-old man with cirrhosis and hepatocellular carcinoma treated by transarterial chemoembolization 3 months earlier. During arterial dominant phase of dynamic MRI, signal intensity of nodule (arrow, B) is still higher than that of surrounding liver on in-phase image, mimicking hypervascular lesion; however, opposed-phase image shows low signal intensity corresponding to nonenhancement (arrow, C) of necrotic tumor.

 

Figure 14
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Fig. 5C 50-year-old man with cirrhosis and hepatocellular carcinoma treated by transarterial chemoembolization 3 months earlier. During arterial dominant phase of dynamic MRI, signal intensity of nodule (arrow, B) is still higher than that of surrounding liver on in-phase image, mimicking hypervascular lesion; however, opposed-phase image shows low signal intensity corresponding to nonenhancement (arrow, C) of necrotic tumor.

 

Figure 15
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Fig. 6A 43-year-old woman with benign lipomatous tumor in fatty liver. Transverse in-phase spoiled gradient-echo MR image (TR/TE, 140/5.3; flip angle, 90°) shows lobulated hyperintense lesion (arrow) in right lobe of liver.

 

Figure 16
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Fig. 6B 43-year-old woman with benign lipomatous tumor in fatty liver. Out-of-phase image (TE, 2.7 msec) shows dark rind of intravoxel phase cancellation at periphery of lesion and at interface between fatty mass and surrounding hepatic parenchyma (arrow). Centrally preserved hyperintensity originates from excessive proportion of fatty content, which is comparable to subcutaneous fat. Geographically decreased signal on background of hepatic parenchyma is due to hepatic steatosis.

 

Figure 17
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Fig. 6C 43-year-old woman with benign lipomatous tumor in fatty liver. High-signal-intensity rind (arrow) on subtraction image reflects intravoxel cancellation area on B.

 

Figure 18
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Fig. 6D 43-year-old woman with benign lipomatous tumor in fatty liver. In-phase arterial phase dynamic MR image shows homogeneously high signal intensity (arrow), suggesting diffuse contrast enhancement of lesion.

 

Figure 19
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Fig. 6E 43-year-old woman with benign lipomatous tumor in fatty liver. Homogeneously decreased signal of lesion (arrow) on out-of-phase arterial phase image suggests paradoxical decrease in signal intensity for enhancing lesions containing excessive fatty component. Intralesional attenuation was approximately -50 H on CT scan (not shown), and nonmalignant cellular fibrosis with abundant fat globules was verified by percutaneous gun needle biopsy.

 

Figure 20
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Fig. 7A 38-year-old man with advanced cirrhosis containing innumerable siderotic nodules. Transverse out-of-phase spoiled gradient-echo MR image (TR/TE, 140/2.7; flip angle, 90°) shows contracted hepatic parenchyma with surface nodularity (arrowheads) surrounded by massive ascites (asterisk) and subcapsular slightly hyperintense lesion (arrow).

 

Figure 21
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Fig. 7B 38-year-old man with advanced cirrhosis containing innumerable siderotic nodules. In-phase image (TE, 5.3 msec) shows high-signal-intensity lesion (arrow) well distinguished from background parenchyma containing innumerable dark-signal-intensity nodules. Darkened signal of siderotic nodules is due to T2* effect with longer TE of in-phase imaging.

 

Figure 22
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Fig. 7C 38-year-old man with advanced cirrhosis containing innumerable siderotic nodules. Subtracted image of out of phase from in phase (B - A) shows "blackout" of hepatic parenchymal signal (arrowheads) due to negative signal value after subtraction. In this situation, presence of fatty component in lesion or background hepatic parenchyma cannot be properly determined. Arrow = subcapsular focal lesion, asterisk = ascites.

 

Figure 23
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Fig. 8A 62-year-old man with chronic hepatitis B virus and diffuse hepatic steatosis complicated by small hepatocellular carcinoma. Transverse in-phase spoiled gradient-echo MR image (TR/TE, 140/5.3; flip angle, 90°) shows slightly hypointense nodule (arrow).

 

Figure 24
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Fig. 8B 62-year-old man with chronic hepatitis B virus and diffuse hepatic steatosis complicated by small hepatocellular carcinoma. Lesion is not well delineated on out-of-phase image (TE, 2.7 msec) because of signal loss from background liver as result of diffuse fat infiltration and consequently decreased lesion-to-liver contrast.

 

Figure 25
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Fig. 8C 62-year-old man with chronic hepatitis B virus and diffuse hepatic steatosis complicated by small hepatocellular carcinoma. Transverse in-phase (C) and out-of-phase (D) dynamic MR images during arterial phase show iso- and mild hyperintensity of lesion, respectively (arrows); these findings suggest hypervascular tumor when compared with unenhanced images. Lesion-to-liver contrast is greater on D than C due to signal loss from background hepatic parenchyma on D.

 

Figure 26
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Fig. 8D 62-year-old man with chronic hepatitis B virus and diffuse hepatic steatosis complicated by small hepatocellular carcinoma. Transverse in-phase (C) and out-of-phase (D) dynamic MR images during arterial phase show iso- and mild hyperintensity of lesion, respectively (arrows); these findings suggest hypervascular tumor when compared with unenhanced images. Lesion-to-liver contrast is greater on D than C due to signal loss from background hepatic parenchyma on D.

 

Figure 27
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Fig. 8E 62-year-old man with chronic hepatitis B virus and diffuse hepatic steatosis complicated by small hepatocellular carcinoma. Transverse in-phase (E) and out-of-phase (F) 5-minute delayed dynamic MR images show decreased signal due to washout of contrast agent (arrows) from lesion. Fibrotic pseudocapsule around lesion is better delineated on F due to signal loss of background parenchyma.

 

Figure 28
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Fig. 8F 62-year-old man with chronic hepatitis B virus and diffuse hepatic steatosis complicated by small hepatocellular carcinoma. Transverse in-phase (E) and out-of-phase (F) 5-minute delayed dynamic MR images show decreased signal due to washout of contrast agent (arrows) from lesion. Fibrotic pseudocapsule around lesion is better delineated on F due to signal loss of background parenchyma.

 

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