Home The T1W Hyperintense Signal on the Surface of Distal Segment of Bile Duct Tumor Thrombi and Its Significance
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The T1W Hyperintense Signal on the Surface of Distal Segment of Bile Duct Tumor Thrombi and Its Significance

Rationale and Objectives

To evaluate the magnetic resonance (MR) findings of bile duct tumor thrombi (BDTT) and intraductal growing-type cholangiocarcinoma (IDG-type CC), especially focusing on the distal segment of intrabiliary tumors.

Materials and Methods

Twenty-nine cases of hepatocellular carcinoma with BDTT and 17 cases of IDG-type CC were available for retrospective review. The following MR findings were evaluated: presence of necrosis and T1-weighted (T1W) hyperintense signal on the surface of the distal segment of intrabiliary tumors, bile duct wall thickening adjacent to the tumor, dilation of bile duct of the tumor-bearing segment, location and maximum diameter of intraductal mass, and presence of a hepatic parenchymal mass.

Results

There was significant difference in T1W hyperintense signal on the surface of the distal segment of intrabiliary tumors between BDTT and IDG-type CC ( P < .05). The T1W hyperintense signal detected in BDTT was identified as bile layering (9/25) or hemobilia (16/25) pathologically. For the diagnosis of BDTT, the sensitivity and specificity of T1W hyperintense signal was 86.2% and 100%, respectively. There was significant difference in necrosis at the distal end of intrabiliary tumors and presence of hepatic parenchymal mass between BDTT and IDG-type CC ( P < .05). However, no statistical significance was found in bile duct dilation, the absence of wall thickening, the location of intraductal mass, or the maximum diameter of intrabiliary mass between the two groups ( P > .05).

Conclusions

The T1W hyperintense signal on the distal segment of intrabiliary mass was because of concentrated bile deposits or hemobilia. The sign of T1W hyper signal on the distal segment is valuable to differentiate BDTT and IDG-type CC.

Hepatocellular carcinoma (HCC) is one of the most common types of malignant abdominal tumors. Jaundice is common in HCC and the incidence is approximately 19% to 40% . The etiology of jaundice is primarily from diffuse tumor infiltration of the liver parenchyma, hilar invasion accompanied by compression of the bile duct, or progressive terminal liver failure . HCC can invade the bile duct and form intrabiliary tumor thrombi . Patients with this type of HCC normally have obstructive jaundice as their initial complaint. Bile duct tumor thrombi (BDTT) formation is presented in 0.8% to 12.9% of surgically resected HCC . Magnetic resonance (MR) imaging is a commonly used diagnostic imaging modality for the detection of hepatic and biliary tumors. The MR manifestation of HCC with BDTT has been reported in the literature . BDTT presents as an intrabiliary cordlike or castlike soft-tissue mass with dilated distal bile duct. However, bile duct wall thickening or tumor invasion beyond bile duct wall is not accompanied in most of the BDTT . On the dynamic-enhanced MR images, early enhancement of BDTT can be detected in the arterial phase . These MR features are very similar to those of intraductal growing-type cholangiocarcinoma (IDG-type CC), which also known as early bile duct carcinoma . These two entities (BDTT and IDG-type CC) are distinct in terms of treatment strategies and prognosis. The prognosis of patients with BDTT is generally poor even with aggressive operative approach, whereas good surgical outcomes can be obtained in IDG-type CC patients after complete resection . For an intrabiliary mass with small hepatic tumor or undetectable liver parenchyma tumor, special emphasis should be placed on discriminating BDTT and IDG-type CC .

Although the MR manifestation of BDTT has been described in detail in the literature, the pathologic change and MR findings of distal segment of BDTT have been rarely reported in the literature. T1-weighted (T1W) hyperintense signal on the surface of distal segment of BDTT has been reported in the literature and is believed to be caused by hemobilia . However, to the best of our knowledge, the pathologic changes and the implications of T1W hyperintense signal on the surface of distal segment of BDTT have not been reported in the literature. To evaluate its significance in the diagnosis of BDTT, we retrospectively reviewed 29 cases of HCC with BDTT and compared the pathologic changes and MR findings of the distal segment of BDTT with those of 17 cases of IDG-type CC. This study mainly focused on the distal segment of BDTT and IDG-type CC.

Materials and methods

Study Population

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MR Imaging

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Table 1

Parameters for MR Imaging

MRI Scanner and Sequence TR/TE (ms) Flip Angle Section Thickness Section Spacing Field of View FST Matrix Size Breath-hold NA 1.5T Gyroscan Intera Axial T1W FFE 260.0/5.0 80° 4.0–6.0 mm 2 mm 360 mm Proset 264 × 207 Yes 1 Axial T2W TSE 1600.0/70.0 90° 4.0–6.0 mm 2 mm 360 mm SPIR 292 × 209 No 3 Coronal T1W FFE 192.0/5.0 80° 5.0 mm 1 mm 400 mm Proset 256 × 204 Yes 1 1.5T Signa HDxt Axial T1W FSPGR 90.0/1.2 80° 6.0 mm 1 mm 350 mm CHESS 320 × 224 Yes 1 Axial T2W FSE 6000.0/86.0 90° 6.0 mm 1 mm 350 mm CHESS 288 × 224 No 2 Coronal T1W FSPGR 75.0/1.3 80° 7.0 mm 1 mm 380 mm CHESS 384 × 224 Yes 1

CHESS, chemical shift selective; FFE, fast field echo; FSE, fast spin echo; FSPGR, fast spoiled gradient echo; FST, fat suppression technique; Proset, principle of selective excitation technique; NA, number of acquisition; SPIR, spectral presaturation inversion recovery; TE, echo time; TR, repetition time; TSE, turbo spin echo.

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Image Evaluation and Pathologic Analysis

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Statistical Analysis

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Results

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Table 2

MRI Findings at the Distal Segment of Intrabiliary Mass in BDTT and IDG-type CC Patients

Findings BDTT ( n = 29) IDG-type CC ( n = 17)P Value T1W hyperintense signal ∗ <.001 Present 25 0 Absent 4 17 Necrosis at the distal end of intrabiliary mass ∗ .001 Present 14 0 Absent 15 17 Bile duct wall thickening adjacent to the tumor † .343 Present 2 3 Absent 27 14 Dilation of bile duct of the tumor-bearing segment † .131 Present 29 15 Absent 0 2 Location of intraductal mass ∗ .885 Extrahepatic duct 22 14 Intrahepatic duct 7 3 Hepatic parenchymal mass ∗ <.001 Present 24 3 Absent 5 14 Maximum diameter of intrabiliary mass ‡ 2.0 ± 0.7 cm 2.2 ± 0.5 cm .366

BDTT, bile duct tumor thrombi; IDG-type CC, intraductal growing-type cholangiocarcinoma.

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Figure 1, Hepatocellular carcinoma with bile duct tumor thrombi (BDTT) in a 56-year-old male. Hyperintense signal on the surface of the distal segment of BDTT ( arrows ) was noted on unenhanced coronal (a) and axial (b) T1-weighted (T1W) images. (c) Hyperintense signal ( arrows ) on the surface of BDTT was detected on the axial T2-weighted (T2W) images, and bile duct dilation can be seen without wall thickening in the tumor-bearing segment. (d) No enhancement was noted in distal segment of the BDTT on the contrast-enhanced T1W images. The resected BDTT specimen (e) and hematoxylin and eosin (HE) staining section (f) showed macroscopic necrotic tissue at the distal end of BDTT and a concentrated bile layer deposited on the surface ( arrows ).

Figure 2, Hepatocellular carcinoma with bile duct tumor thrombi (BDTT) in a 48-year-old male. Hyperintense signal on the surface of the distal segment of BDTT ( arrows ) was noted on unenhanced coronal (a) and axial (b) T1-weighted (T1W) images. (c) Hypointense signal ( arrows ) on the surface of BDTT was demonstrated on the axial T2-weighted (T2W) images, and bile duct dilation can be seen without wall thickening in the tumor-bearing segment. (d) No bile duct wall thickening ( arrows ) was noted in the tumor-bearing segment on the contrast-enhanced T1W images. (e) The hematoxylin and eosin (HE) staining section revealed hemorrhagic layer on the distal end of the BDTT ( arrows ).

Figure 3, Hepatocellular carcinoma with bile duct tumor thrombi (BDTT) in a 60-year-old male. Hyperintense signal on the surface of the distal segment of BDTT ( arrows ) was noted on unenhanced coronal (a) and axial (b) T1-weighted (T1W) images. (c) Homogeneous enhancement ( arrow ) was noted in the distal segment of BDTT on contrast-enhancement T1W images. The resected BDTT specimen (d) and hematoxylin and eosin (HE) staining section (e) showed a hemorrhagic layer on the distal end of the BDTT ( arrows ), and the distal segment of BDTT was with viable tumor without macroscopic necrosis.

Figure 4, A 73-year-old female with intraductal growing-type cholangiocarcinoma (IDG-type CC). No hyperintense signal on the surface of the distal segment of bile duct tumor ( arrows ) was noted on unenhanced coronal (a) and axial (b) T1-weighted (T1W) images. (c) The axial T2-weighted (T2W) images revealed a well-circumscribed intrabiliary tumor, and bile duct dilation can be seen without wall thickening in the tumor-bearing segment ( arrows ). (d) Homogeneous enhancement was noted in the distal segment of the IDG-type CC on the contrast-enhancement T1W images ( arrows ). The resected BDTT specimen (e) and hematoxylin and eosin (HE) staining section (f) showed viable tumor tissue at the distal segment of the IDG-type CC, and no concentrated bile layer or hemorrhage was observed.

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Discussion

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