Magnetic Resonance Imaging Features of Uncomplicated Hepatic Adenoma: a case report

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1 Chin J Radiol 2003; 28: Magnetic Resonance Imaging Features of Uncomplicated Hepatic Adenoma: a case report MING-MING WU 1 CHEN-CHU CHANG 1 SONG-SHEI LIN 3 JEN-I HWANG 2 TAIN LEE 2 YEU-SHENG TYAN 2,3 SAN-KAN LEE 2 Department of Radiology 1, Army Taichung General Hospital Department of Radiology 2, Taichung Veterans General Hospital Department of Radiological Technology 3, Chung Tai Institute of Health Sciences and Technology Hepatic adenomas (HAs) are incidentally detected with increasing frequency after imaging the abdomen for unrelated pathology. We report the radiological findings in an asymptomatic 47-yearold female with an uncomplicated HA, who received the subcutaneous implant of contraceptive Norplan six years ago. MRI showed a well-defined mass in the liver, which was isointense in the T1-weighted and fat-suppressed T2-weighted images, but became hypointense in the fat-suppressed T1-weighted images. Enhanced dynamic scan showed minimal enhancement in the arterial phase. Recognition of such MRI features will help us to suggest the possibility of uncomplicated HAs in the appropriate clinical setting. Key words: Adenoma; Contraceptive; Computed tomography; Magnetic resonance imaging Hepatic adenoma (HA) is a rare benign lesion that is most often seen in young women with a history of oral contraceptive usage [1, 2]. It is typically solitary, although multiple lesions have been reported, particularly in patients with glycogen storage disease and liver adenomatosis [3-5]. Because of the risk of hemorrhage [6] and malignant transformation [7], HAs must be identified and treated promptly. Most HAs are not specifically diagnosed by ultrasonography and are usually further evaluated with CT or other imaging modalities. Multiphasic helical CT and MRI allow more accurate detection and characterization of focal hepatic lesions. Herein we report the radiological features of a case of HA not complicated with intratumoral hemorrhage or infarction. The MRI findings are stressed because of its interesting tissue characterization features. Understanding the imaging appearance of HA can help us to avoid misdiagnosis and facilitate prompt, effective treatment. CASE REPORT Reprint requests to: Dr. Yeu-Sheng Tyan Department of Radiology, Taichung Veterans General Hospital. No. 160, Sec. 3, Taichung Kang Road, Taichung 407, Taiwan, R.O.C. A homogeneous hyperechoic nodular lesion about 2 cm in size was incidentally noted in the S5 of liver in a 47-year-old female during the routine physical check-up with sonography. This nodule showed no definite calcification, cystic change or capsule formation. Subsequent CT (Picker 5000, USA) examination revealed a low attenuation nodule in the S5 region in the nonenhanced scan (Fig 1a), and mild enhancement in the arterial (Fig.1b) phase of the enhanced dynamic scans. Additionally, a small hypervascular nodule at the S8 region showed typical appearance of hemangioma with high attenuation in the arterial phase and persistent enhancement in the delayed phase. In MRI (GE Signa 1.5T, USA), the nodule in S5 was barely visible in the Fast Spoiled Gradient Echo (FSPGR) T1- weighted images (Fig. 2a), but was clearly identified in

2 110 MRI of hepatic adenoma the fat-suppressed FSPGR T1-weighted images (Fig.2b). In the Single Shot Fast Spin Echo (SSFSE) T2-weighted images with fat suppression, the lesion was almost isodensity compared with surrounding liver parenchyma (Fig 2c). The dynamic studies were performed with fat-suppressed FSPGR T1-weighted 2a 1a 2b 1b 2c 1c Figure 1. Triphasic CT for the liver: a. is the precontrast scan, b. and c. represent arterial and delayed phases respectively. Note mild homogeneous enhancement (arrow) in the arterial phase b. Figure 2. a. Axial FSPGR T1-weighted image (TR/TE= 220/4.2 ms, flip angle=80 ) and c. SSFSE fat-suppressed T2-weighted image (29232/67.7 ms) barely showed the tumor. The lesion was easily identified in the b. fatsuppressed FSPGR T1-weighted image (220/1.5 ms, flip angle=80 ) (arrow)

3 MRI of hepatic adenoma 111 3a 3b 3c 3d Figure 3. Enhanced dynamic studies with axial fat-suppressed FSPGR T1-weighted image (220/1.5 ms, flip angle=80 ) at b. 20-s, c. 90-s and d. 3-min phases showed only minimal enhancement of the S5 nodule in the arterial phase b. The pre-contrast image is shown in a.. imaging sequences with intravenous administration of Gd-DTPA 10 ml at the rate of 3 ml/sec. The hepatic arterial phase, portal venous phase and delayed phase were taken at 20 seconds, 90 seconds, and 3 minutes respectively after intravenous contrast medium injection. As in CT, this nodule showed only slightly enhancement in the arterial phase (Fig.3). Angiography of the common hepatic artery showed no definite tumor vessel or tumor stain in S5 region, while a small hypervascular nodule with dense and prolonged stain was identified in S8 region, typical for hemangioma. The laboratory data was not contributory, including the liver function test, markers for the HBV and HCV infections, and tumor markers (carcinoembryonic antigen and alpha fetal protein). Tracing the past history, this patient received the subcutaneous implant of contraceptive Norplant 6 years ago, which was removed 1 year before admission. Subsequently, the patient received exploratory laparotomy and wedge resection for the liver nodule in the S5. The pathological report was a HA with abundant microvesicular steatosis. No definite tumor capsule, intratumoral hemorrhage or infarction was seen. The post-operative course was smooth and the patient was discharged 4 days later. DISCUSSION HAs are benign, rare tumors that occur primarily in women with a history of oral contraceptive use [1, 2]. Surgical treatment is recommended to reduce the risk of sudden, unpredictable hemorrhage or malignant transformation [8, 9]. The diagnostic difficulty in distinguishing HA from a well-differentiated hepatoma is another reason for an aggressive treatment [10]. The relationship between HA and oral contraceptives has been well documented and there have been several reports of tumor regression after the withdraw-

4 112 MRI of hepatic adenoma al of hormonal agents [11]. However, not all HAs regress in this manner, like what happened in our patient, who had removed the subcutaneous contraceptive one year before the admission after a six-year implantation. Moreover, in some cases of tumor regression, malignant degeneration was reported in the area of the previous HA [12, 13]. The unpopularity of contraceptive in the childbearing women may possibly explain the rarity of HA in Taiwan. The appearance of HAs on different imaging modalities is highly variable because of their varied histopathology, and images of HAs are at times indistinguishable from those of other hepatic tumors, such as well-differentiated hepatocellular carcinoma or focal nodular hyperplasia [14]. The MRI features of the uncomplicated HA varies, but are typically only mildly hyper- or hypointense in the T1- or T2-weighted images [15], reflecting its similarity to the normal parenchyma. In the previous report (8), over half (59%) HA showed mild hyperintense in the T1- weighted images, and the degree of hyperintensity is related to the quantity of fat or the presence of hemorrhage [15]. In the T1- weighted images of our case (Fig.2a), the tumor is almost iso-intense with surrounding liver parenchyma. While less common, isointensity in the T1- weighted images did occur in 6% cases in previous reported series of HA [15]. In spite of the fact that intracellular steatosis is thought to have a shorter T1 relaxation time than normal liver, recent report has noted that different ultrastructural alterations in the subcellular organelles of hepatocytes can alter the MR tissue parameters as well [16], which may explain the diversity of signal intensities of HAs in the T1WI. Typically, the signal intensity of HA will decrease in the out-ofphase or fat-suppressed sequences due to its abundant fat [15, 17]. In our case, the lesion became hypointense in the fat-suppressed T1- weighted images (Fig 2b). The substantial fat content was confirmed in the histological specimen (Fig.4). In the T2- weighted images, HA could be either mildly hyperintense or hypointense [8, 15, 17]. The lesion of our case showed almost isointensity in the fat-suppressed T2- weighted imaging (Fig.2c), supposedly would be hyperintense in the T2- weighted image without fatsuppression, which was not included in our routine imaging protocols for the liver. On the other hand, heterogeneous intensity of HA is not uncommon, reflecting the frequent occurrence of intratumoral hemorrhage and necrosis. This feature sometimes makes the diagnosis easier if it occurs in the correct clinical context (contraceptive usage). However, the histological specimen in our case (Fig.4) confirmed Figure 4. Photomicrograpy (PAS, x100) of the specimen showed abundant intracellular fat in the HA (arrow), in contrast to the adjacent normal liver parenchyma (arrowheads) the absence of any intratumoral bleeding or necrosis, which was reflected in the homogeneity of the tumor in MRI. In the dynamic study, HA characteristically exhibits an immediate faint blush in the arterial phase, which rapidly fades in the venous phase [17], as shown in our case (Fig 1,3). The intratumoral fat is not specific for HA [18]. Hepatic angiomyolipoma, lipoma, hepatoma and focal nodular hyperplasia are examples of the list that might contain fat. According to Paulson [15], 68% (15/22) histologically examined HA specimen contained fat of grade 2 or 3 (defined as fat present in over one third of the cells of the HA). However, a homogeneous drop of signal intensity in the out-of-phase or fat-suppressed images rarely occurred in other tumors [19]. The differentiation of HA from focal fatty infiltration of liver is also important, which is easily accomplished by the transient enhancement after gadolinium administration in HA. REFERRENCE 1. Edmonson H, Henderson B, Benton B. Liver cell adenomas associated with use of cotraceptives. N Engl J Med. 1976; 249: Rooks J, Ory H, Ishak K, et al. Epidemiology of hepatocellular adenoma. JAMA. 1979; 242: Grossman H, Ram PC, Coleman RA, et al. Hepatic ultrasonography in type I glycogen storage disease (von Gierke disease). Detection of hepatic adenoma and carcinoma. Radiology 1981; 141: Horton WA, Calli LJ, Jr. Multiple endocrine adenomatosis presenting as Zollinger-Ellison syndrome, nonbeta islet cell adenoma, parathyroid adenoma, renal calculi, bronchial carcinoid, insulinoma, hepatic hamartoma, etc. Birth Defects Orig Artic Ser 1971; 7: Flejou JF, Barge J, Menu Y, et al. Liver adenomatosis: an entity distinct from liver adenoma? Gastroenterology

5 MRI of hepatic adenoma ; 83: Sears HF, Smith G, Powell RD. Hepatic adenoma associated with oral contraceptive use: an unusual clinical presentation. Arch Surg 1976; 111: Pimparkar BD, Bhalerao RA, Deodhar KP, Nerurkar MG, Mehta JM. Hepatic adenoma with malignant change: a case report. J Assoc Physicians India 1972; 20: Arrive L, Flejou JF, Vilgrain V, et al. Hepatic adenoma: MR findings in 51 pathologically proved lesions. Radiology 1994; 193: Gyorffy EJ, Bredfeldt JE, Black WC. Transformation of hepatic cell adenoma to hepatocellular carcinoma due to oral contraceptive use. Ann Intern Med 1989; 110: Weil R, 3rd, Koep LJ, Starzl TE. Liver resection for hepatic adenoma. Arch Surg 1979; 114: Aseni P, Sansalone CV, Sammartino C, et al. Rapid disappearance of hepatic adenoma after contraceptive withdrawal. J Clin Gastroenterol 2001; 33: Leese T, Farges O, Bismuth H. Liver cell adenoma: a 12-year surgical experience from a special hepato-biliary unit. Ann Surg 1988; 208: Gordon SC, Reddy KR, Livingstone AS, Jeffers LJ, Schiff ER. Resolution of a contraceptive-steroidinduced hepatic adenoma with subsequent evolution into hepatocellular carcinoma. Ann Intern Med 1986; 105: Herman P, Pugliese V, Machado MA, et al. Hepatic adenoma and focal nodular hyperplasia: differential diagnosis and treatment. World J Surg 2000; 24: Paulson EK, McClellan JS, Washington K, Spritzer CE, Meyers WC, Baker ME. Hepatic adenoma: MR characteristics and correlation with pathologic findings. Am J Roentgenol 1994; 163: Chai JW, Lin YC, Chen JH, et al. In vivo magnetic resonance (MR) study of fatty liver: importance of intracellular ultrastructural alteration for MR tissue parameters change. J Magn Reson Imaging 2001; 14: Grazioli L, Federle MP, Brancatelli G, Ichikawa T, Olivetti L, Blachar A. Hepatic adenomas: imaging and pathologic findings. Radiographics 2001; 21: Itai Y, Ohtomo K, Kokubo T, et al. CT and MR imaging of fatty tumors of the liver. J Comput Assist Tomogr 1987; 11: Semelka RC, Braga L, Armao D, et al., ed. Liver. In: Semelka RC Abdominal-Pelvic MRI. 1st ed. New York, Wiley-Liss, Inc., 2002: 84-91

6 114 MRI of hepatic adenoma

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