1.Drug Induced Hepatitis Mimicking Alcoholic Hepatitis.
The Korean Journal of Hepatology 2006;12(4):574-578
2.The significance of anti-HBc and occult hepatitis B virus infection in the occurrence of hepatocellular carcinoma in patients with HBsAg and anti-HCV negative alcoholic cirrhosis.
Min Ju KIM ; Oh Sang KWON ; Nak So CHUNG ; Seo Young LEE ; Hyuk Sang JUNG ; Dong Kyun PARK ; Yang Suh KU ; Yu Kyung KIM ; Yun Soo KIM ; Ju Hyun KIM
The Korean Journal of Hepatology 2008;14(1):67-76
BACKGROUND/AIMS: Alcohol and the hepatitis B virus (HBV) exert synergistic effects in hepatocelluar carcinogenesis. We aimed to elucidate the clinical significance of the antibody to hepatitis B core antigen (anti-HBc) and occult HBV infection on the development of hepatocellular carcinoma (HCC) in patients with alcoholic liver cirrhosis (LC). METHODS: Patients with alcoholic LC alone (n=193) or combined with HCC (n=36), who did not have HBsAg or antibody to hepatitis C virus were enrolled. Clinical data and laboratory data including anti-HBc were investigated at enrollment. The polymerase chain reaction was applied to HBV DNA using sera of patients with HCC or LC after age and sex matching. RESULTS: Patients with HCC were older (60+/-11 years vs. 53+/-10 years, mean+/-SD, P<0.001), more likely to be male (100% vs. 89%, P=0.03), and had a higher positive rate of anti-HBc (91.2% vs. 77.3%, P=0.067), and a higher alcohol intake (739+/-448 kg vs. 603+/-409 kg, P=0.076) than those with LC. Age was the only significant risk factor for HCC revealed by multiple logistic regression analysis (odds ratio, 1.056; P=0.003). The positive rate of anti-HBc and alcohol intake did not differ in age- and sex-matched subjects between the LC (n=32) and HCC (n=31) groups. However, the detection rate of serum HBV DNA was higher in the HCC group (48.4%) than in the LC group (0%, P<0.001). CONCLUSIONS: Anti-HBc positivity is not a risk factor for HCC. However, occult HBV infection may be a risk factor for HCC in patients with alcoholic LC.
Adult
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Aged
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Antibodies, Viral/blood
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Carcinoma, Hepatocellular/diagnosis/epidemiology/*etiology
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DNA, Viral/analysis
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Female
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Hepatitis B/*complications/diagnosis
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Hepatitis B Core Antigens/*immunology
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Hepatitis B Surface Antigens/immunology
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Hepatitis B virus/genetics/immunology/isolation & purification
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Hepatitis C/complications/diagnosis
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Humans
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Liver Cirrhosis, Alcoholic/*complications/diagnosis/epidemiology
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Liver Neoplasms/diagnosis/epidemiology/*etiology
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Male
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Middle Aged
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Risk Factors
4.Type and cause of liver disease in Korea: single-center experience, 2005-2010.
Sang Soo LEE ; Young Sang BYOUN ; Sook Hyang JEONG ; Yeo Myung KIM ; Ho GIL ; Bo Young MIN ; Mun Hyuk SEONG ; Eun Sun JANG ; Jin Wook KIM
Clinical and Molecular Hepatology 2012;18(3):309-315
BACKGROUND/AIMS: The aim of this study was to describe the types and causes of liver disease in patients from a single community hospital in Korea between April 2005 and May 2010. METHODS: A cohort of patients who visited the liver clinic of the hospital during the aforementioned time period were consecutively enrolled (n=6,307). Consistent diagnostic criteria for each liver disease were set by a single, experienced hepatologist, and the diagnosis of all of the enrolled patients was confirmed by retrospective review of their medical records. RESULTS: Among the 6,307 patients, 528 (8.4%) were classified as acute hepatitis, 3,957 (62.7%) as chronic hepatitis, 767 (12.2%) as liver cirrhosis, 509 (8.1%) as primary liver cancer, and 546 (8.7%) as a benign liver mass or other diseases. The etiologies in the acute hepatitis group in decreasing order of prevalence were hepatitis A (44.3%), toxic hepatitis (32.4%), other hepatitis viruses (13.8%), and cryptogenic hepatitis (9.1%). In the chronic hepatitis group, 51.2% of cases were attributed to viral hepatitis, 33.3% to nonalcoholic fatty liver disease, and 13.0% to alcoholic liver disease (ALD). Of the cirrhoses, 73.4% were attributable to viral causes and 18.1% to alcohol. Of the hepatocellular carcinoma cases, 86.6% were attributed to viral hepatitis and 11.6% to ALD. Among the benign tumors, hemangioma comprised 52.2% and cystic liver disease comprised 33.7%. CONCLUSIONS: Knowledge of the current status of the type and cause of liver disease in Korea may be valuable as a basis for evaluating changing trends in liver disease in that country.
Acute Disease
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Adolescent
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Adult
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Aged
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Aged, 80 and over
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Alcohol Drinking/adverse effects
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Carcinoma, Hepatocellular/epidemiology/etiology/pathology
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Chronic Disease
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Cohort Studies
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Fatty Liver/epidemiology
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Female
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Hepatitis/epidemiology
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Hepatitis, Viral, Human/complications/epidemiology
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Humans
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Liver Cirrhosis/epidemiology/etiology
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Liver Diseases/*diagnosis/epidemiology
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Liver Diseases, Alcoholic/complications/epidemiology
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Liver Neoplasms/epidemiology/etiology/pathology
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Male
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Middle Aged
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Prevalence
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Republic of Korea/epidemiology
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Retrospective Studies
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Young Adult
5.Clinical Features of Non-alcoholic Fatty Liver Disease in Cryptogenic Hepatocellular Carcinoma.
Min Young RIM ; Oh Sang KWON ; Minsu HA ; Ju Seung KIM ; Kwang Il KO ; Dong Kyu KIM ; Pil Kyu JANG ; Jung Yoon HAN ; Pyung Hwa PARK ; Young Kul JUNG ; Duck Joo CHOI ; Yun Soo KIM ; Ju Hyun KIM
The Korean Journal of Gastroenterology 2014;63(5):292-298
BACKGROUND/AIMS: Nonalcoholic fatty liver disease (NAFLD) may be one of the important causes of cryptogenic hepatocellular carcinoma (HCC). The aim of this study was to evaluate whether patients with cryptogenic HCC share clinical features similar to that of NAFLD. METHODS: Cryptogenic HCC was defined as HCC that occurs in patients with the following conditions: HBsAg(-), anti-HCV(-), and alcohol ingestion of less than 20 g/day. All patients diagnosed with cryptogenic HCC from 2005 to 2012 (cryptogenic HCC group), and all patients diagnosed with HBV associated HCC between 2008 and 2012 (HBV-HCC group) were enrolled in the present study. Clinical features, BMI, lipid profiles, presence of diabetes mellitus, hypertension, and metabolic syndrome were compared between the two groups. RESULTS: Cryptogenic HCC group was composed of 35 patients (19 males and 16 females) with a mean age of 70+/-11 years. HBV-HCC group was composed of 406 patients (318 males and 88 females) with a mean age of 56+/-7 years. Patients in the cryptogenic HCC group were older (p=0.001) and female dominant (p=0.042) than those in the HBV-HCC group. There were no differences in the laboratory test results including lipid profiles and Child-Turcotte-Pugh class between the two groups. Patients in the cryptogenic HCC group had higher prevalence of diabetes (37% vs. 17%, p=0.015), hypertension (49% vs. 27%, p=0.051), metabolic syndrome (37% vs. 16%, p=0.001), and higher BMI (25.3 kg/m2 vs. 24.1 kg/m2, p=0.042) than those in the HBV-HCC group. The tumor stage was more advanced (stage III and IV) at diagnosis in the cryptogenic HCC group than in the HBV-HCC group (60% vs. 37%, p=0.007). CONCLUSIONS: Cryptogenic HCC has clinical features similar to that of NAFLD and is diagnosed at a more advanced tumor stage.
Age Factors
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Aged
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Body Mass Index
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Carcinoma, Hepatocellular/*diagnosis/etiology/pathology
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Diabetes Complications
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Diabetes Mellitus/pathology
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Female
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Hepatitis B/complications
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Humans
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Hypertension/complications
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Lipids/blood
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Liver Neoplasms/*diagnosis/etiology/pathology
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Male
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Metabolic Syndrome X/complications
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Middle Aged
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Neoplasm Staging
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Non-alcoholic Fatty Liver Disease/*diagnosis/pathology
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Risk Factors
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Severity of Illness Index
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Sex Factors