1.Some trends in liver fibrosis research.
Chinese Journal of Hepatology 2006;14(3):167-168
Humans
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Liver Cirrhosis
;
diagnosis
;
pathology
;
therapy
2.Points in pathological diagnosis of chronic hepatitis.
Chinese Journal of Hepatology 2007;15(5):383-384
Biopsy
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Hepatitis, Chronic
;
diagnosis
;
pathology
;
Humans
;
Liver Cirrhosis
;
diagnosis
;
pathology
4.A Case of Primary Biliary Cirrhosis.
Se Woo PARK ; Hang Lak LEE ; Ho Soon CHOI
The Korean Journal of Gastroenterology 2006;48(6):375-377
No abstract available.
Female
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Humans
;
Liver Cirrhosis, Biliary/*diagnosis/pathology/radiography
;
Middle Aged
5.Hepatocarcinogenesis in liver cirrhosis: imaging diagnosis.
Journal of Korean Medical Science 1998;13(2):103-116
Hepatocellular carcinoma (HCC) frequently occurs in association with liver cirrhosis, as chronic liver disease is one of the most important factors in carcinogenesis. In addition to HCCs, recent reports of pathologic studies of resected specimens from cirrhotic liver describe associated small nodular lesions such as regenerative nodule, dysplastic nodule (adenomatous hyperplasia), and dysplastic nodule with subfocus of HCC (early HCC). In hepatocarcinogenesis of the cirrhotic liver, a regenerative nodule might be the first step in the development of HCC, going through phases of dysplastic nodule, early HCC and early advanced HCC in a multistep fashion. Fortunately, recent advances in various imaging techniques have facilitated the verification of these nodules. In this review, new nomenclature of small hepatocellular nodules, and detection and characterization of hepatic nodules in carcinogenesis with various imaging techniques are described with focus on the premalignant lesions and early stage of HCC. In addition, the efficacy of various imaging techniques for diagnosing them is discussed. Although the terms and definitions of these nodules are still variable and controversial, familiarity with the concept of these borderline lesions is important.
Carcinoma, Hepatocellular/pathology
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Carcinoma, Hepatocellular/diagnosis*
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Carcinoma, Hepatocellular/complications
;
Diagnostic Imaging*/methods
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Human
;
Liver Cirrhosis/pathology
;
Liver Cirrhosis/diagnosis*
;
Liver Cirrhosis/complications
;
Patient Care Management
;
Terminology
7.Progress in non-invasive diagnostic model of hepatic fibrosis.
Bao-En WANG ; Ji-Dong JIA ; Wen-Sheng ZHANG
Chinese Journal of Integrated Traditional and Western Medicine 2006;26(1):5-7
Biomarkers
;
blood
;
Biopsy, Needle
;
utilization
;
Hepatitis C
;
complications
;
Humans
;
Liver
;
pathology
;
Liver Cirrhosis
;
diagnosis
;
pathology
8.A Case of Nodular Regenerative Hyperplasia of Liver that mimicked Primary Biliary Cirrhosis.
Sung Gon SHIM ; Joo Hyun SOHN ; Jae Woong LEE ; Young Woo CHUNG ; Chang Hee PAIK ; Jong Pyo KIM ; Yong Chul JEON ; Dong Soo HAN ; Joon Soo HAHM ; Dong Hoo LEE ; Choon Suhk KEE ; Young Ha OH
The Korean Journal of Hepatology 2004;10(4):313-318
Nodular regenerative hyperplasia (NRH) of the liver is a rare disease that is characterized by multiple regenerative nodules in the hepatic parenchyma without fibrosis. The exact pathogenesis of NRH has not been established, but it's been suggested that obliteration of portal veins may initiate the nodular transformation. It is also known that this disease is associated with autoimmune disease, myeloproliferative disease, lymphoproliferative disease, primary biliary cirrhosis, and some chemotherapy agents. The patients with NRH are usually asymptomatic, yet if they have symptoms, the most common clinical manifestations are those of portal hypertension, including splenomegaly and esophageal varices with or without bleeding. We report a case of nodular regenerative hyperplasia that presented with clinical manifestations similar to those of primary biliary cirrhosis.
Aged
;
Diagnosis, Differential
;
English Abstract
;
Female
;
Focal Nodular Hyperplasia/*diagnosis/pathology
;
Humans
;
Hyperplasia
;
Liver/*pathology
;
Liver Cirrhosis, Biliary/*diagnosis
9.Primary Sclerosing Cholangitis.
The Korean Journal of Hepatology 2004;10(2):154-157
No abstract available.
Adult
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Cholangitis, Sclerosing/*diagnosis/pathology
;
Diagnosis, Differential
;
Humans
;
Liver Cirrhosis, Biliary/diagnosis
;
Male
10.Comparison of magnetic resonance elastography and diffusion-weighted imaging for staging hepatic fibrosis.
Li-Qiu ZOU ; Jie CHEN ; Liang PAN ; Jin-Zhao JIANG ; Wei XING
Chinese Medical Journal 2015;128(5):620-625
BACKGROUNDTo compare the diagnostic values of magnetic resonance elastography (MRE) and diffusion-weighted imaging (DWI) in staging hepatic fibrosis (HF) in an animal model.
METHODSThis study consisted of 44 rabbits served as HF group and 9 normal rabbits. HF group was divided into two subgroups: Group A (n = 32) and Group B (n = 12). Rabbits in Group B were served as a complementary group when rabbits in Group A suddenly died during the study. Rabbits from control and Group A underwent abdominal MR imaging (MRI), MRE, and DWI. In Group A, random eight rabbits underwent MRI examinations at 4, 5, 6, 10 weeks after carbon tetrachloride oil subcutaneous injection. Liver stiffness (LS) and apparent diffusion coefficient (ADC) values of liver parenchyma were measured. The diagnostic performance of MRE and DWI for staging HF was compared using the receiver operating characteristic curve analysis on the basis of the histopathological analysis of HF.
RESULTSSignificant differences of LS and DWI values were present among HF stages (P < 0.005). The LS values measured on MRE (r = 0.838, P < 0.001) were more strongly correlated with the HF stages than with ADC values (r = -0.527, P < 0.001). The area under the receiver operating characteristic curve values of LS were significantly larger than those of DWI were for discriminating two stages of HF (0.979 vs. 0.712 for ≥ S1, 0.922 vs. 0.699 for ≥ S2). MRE showed higher specificity for predicting all stages of HF compared to DWI.
CONCLUSIONSMRE more strongly correlated with the HF stages than DWI and is more specific in predicting all HF stages.
Animals ; Diffusion Magnetic Resonance Imaging ; methods ; Elasticity Imaging Techniques ; methods ; Liver ; pathology ; Liver Cirrhosis ; diagnosis ; Rabbits