2.Development of prognostic models of liver diseases.
Jun-yong ZHANG ; Fu-kui ZHANG ; Ji-dong JIA ; Bao-en WANG
Chinese Journal of Hepatology 2005;13(11):876-877
5.A Case of Idiopathic Hypereosinophilic Syndrome with Hepatic Involvement in a 5-Year-Old Boy.
Young Mi KIM ; Yoon Jin LEE ; Jae Hong PARK ; Jun Woo LEE ; Chang Hun LEE
The Korean Journal of Hepatology 2002;8(3):321-326
Idiopathic hypereosinophilic syndrome is defined as the presence of prolonged eosinophilia without an identifiable underlying cause and with evidence of end-organ dysfunction. The organs involved are the heart, bone marrow, nervous system, lungs, liver, skin, and gastrointestinal tract. Hepatic involvement is found in about 30% of patients of idiopathic hypereosinophilic syndrome. It occurs rarely in infants and children. In this report, we experienced one case of idiopathic hypereosinophilic syndrome with hepatic involvement in a 5-year-old boy who complained of intermittent fever and right upper quadrant abdominal pain. An abdominal ultrasound examination revealed an ill-defined low-echoic lesion in the liver. Pathologic findings of a biopsy specimen clearly showed the infiltration of eosinophils in the liver. Laboratory data disclosed absolute eosinophilia. There was no evidence of allergic disease or parasitic infestation.
Child, Preschool
;
English Abstract
;
Eosinophils/pathology
;
Human
;
Hypereosinophilic Syndrome/*complications/diagnosis
;
Liver/pathology
;
Liver Diseases/*complications/diagnosis/pathology
;
Male
6.Irreformable hyponatremia: a case report of pituitary dysfunction with liver cirrhosis.
Jing ZHONG ; Yan CHEN ; Liang-jing WANG
Chinese Medical Journal 2011;124(14):2234-2236
The diagnosis of pituitary dysfunction is very difficult in inpatients with liver cirrhosis, because the symptoms are intricate and similar. We here report a case of a male patient complaining of fatigue and anorexia for more than two years. On duration of hospital stay, hyponatremia was irreformable. Magnetic resonance imaging of the pituitary revealed the presence of cystic pituitary and abnormal signal in the left frontal lobe. The patient was also suspected to be infective endocarditis. Recognition of this unusual complication of this condition is important for the patients with chronic liver disease.
Endocarditis
;
diagnosis
;
Humans
;
Hyponatremia
;
diagnosis
;
Liver Cirrhosis
;
complications
;
Male
;
Middle Aged
;
Pituitary Diseases
;
diagnosis
7.Current status of liver diseases in Korea: Toxic and alcoholic liver diseases.
The Korean Journal of Hepatology 2009;15(Suppl 6):S29-S33
The study of the epidemiology of toxic liver injury has been limited in Korea. The number of hospitalizations for toxic liver injury has been estimated to be 2,400 persons per year. About 30~40% of fulminant hepatitis was attributed to toxic hepatitis. The frequent causative agents of toxic hepatitis in Korea are herbal medicines (34~40%), folk remedies (23~34%), and prescribed medicines (24~55%). However, the most common agents causing severe liver injury including fulminant hepatitis are herbal medicine and folk remedies. Antituberculosis drugs and acetaminophen are two common causes of fulminant hepatitis among prescribed drugs. Alcohol is one of the leading causes of chronic liver disease in Korea. No nationwide study on the epidemiology of alcoholic liver disease (ALD) has been carried out, but 7~31% of cirrhosis has been reported to be alcoholic in a few single-center studies. Alcohol could be a risk factor for the development of hepatocellular carcinoma (HCC) in chronic viral hepatitis. Several studies have shown that alcohol increased the risk of HCC in liver cirrhosis with HBsAg or anti-HCV. Furthermore, alcoholic cirrhosis with occult hepatitis B virus infection increased the risk of HCC.
Drug-Induced Liver Injury/diagnosis/*epidemiology/etiology
;
Humans
;
Korea/epidemiology
;
Liver Cirrhosis, Alcoholic/complications/epidemiology
;
Liver Diseases, Alcoholic/complications/*epidemiology
;
Liver Neoplasms/etiology
;
Risk Factors
8.Clinical features of different clinical forms of childhood congenital hepatic fibrosis.
Xin WU ; Xiao-Rang DU ; Jin-Fang DING ; Meng-Jin WU ; Sheng-Qiang LUO ; Xing-Zhong FENG
Chinese Journal of Contemporary Pediatrics 2016;18(4):335-339
OBJECTIVETo compare the clinical features of children with different clinical forms of congenital hepatic fibrosis (CHF), and provides a description of the characteristics of childhood CHF.
METHODSSixty children with CHF between January 2002 and June 2015 were enrolled, including 26 children with portal hypertensive CHF (PH CHF), 3 children with cholangitic CHF, 30 children with combined portal hypertensive and cholangitic CHF (mixed CHF), and 1 child with latent forms of CHF. The medical data of 26 children with PH CHF and 30 children with mixed CHF, including gender, age, clinical manifestations, physical signs, laboratory tests and imaging characteristics, were retrospectively studied.
RESULTSFever, jaundice and hepatomegaly were more frequently noted in children with mixed CHF than in those with PH CHF (P<0.05). Splenomegaly and liver cirrhosis occurred more often in children with CHF, but there was no significant difference in the incidences of splenomegaly and liver cirrhosis between the children with PH CHF and mixed CHF. The plasma prothrombin activity, white blood cell counts, platelet counts, mean platelet volume, serum levels of alanine transaminase, aspartate transaminase, alkaline phosphatase, γ-glutamyl transferase, leucine aminopeptidase, and total bile acids in children with mixed CHF were higher than in those with PH CHF (P<0.05). The decreased international normalized ratio and lower serum albumin levels were more frequently observed in children with mixed CHF than in those with PH CHF (P<0.05).
CONCLUSIONSPH and mixed CHF are common forms in childhood CHF. The children with the two forms of PH usually manifest portal hypertension such as cirrhosis and hepatosplenomegaly. The liver damage may be common in children with mixed CHF.
Adolescent ; Alkaline Phosphatase ; blood ; Child ; Female ; Genetic Diseases, Inborn ; complications ; diagnosis ; Humans ; Liver Cirrhosis ; complications ; diagnosis ; Male ; Splenomegaly ; etiology
9.Multiple Pyogenic Liver Abscesses Caused by Microperforation of an Idiopathic Cecal Ulcer.
Dong Han YEOM ; Ki Chang SOHN ; Min Su CHU ; Dong Ho JO ; Eun Young CHO ; Haak Cheoul KIM
The Korean Journal of Gastroenterology 2016;67(1):44-48
Idiopathic cecal ulcer is a rare disease entity of unknown cause diagnosed by ruling out other known causes of cecal ulceration. The most common complication of an idiopathic cecal ulcer is bleeding; perforation, peritonitis, abscess, and stricture formation have been noted. The authors treated a 53-year-old woman who presented with fever and intermittent right upper quadrant abdominal pain. Multiple pyogenic liver abscess and a solitary cecal ulcer were diagnosed by radiologic, endoscopic, and pathologic examination, followed by laparoscopic cecectomy. After extensive study, we concluded that this patient's liver abscesses were a complication of the idiopathic cecal ulcer. Herein, we report a case of multiple pyogenic liver abscess caused by microperforation of idiopathic cecal ulcer.
Cecal Diseases/complications/*diagnosis/surgery
;
Colonoscopy
;
Female
;
Humans
;
Laparoscopy
;
Liver/pathology
;
Liver Abscess, Pyogenic/*diagnosis/etiology
;
Middle Aged
;
Tomography, X-Ray Computed
;
Ulcer/complications/*diagnosis/surgery
10.Development of a Rating System for Digestive System Impairments: Korean Academy of Medical Sciences Guideline.
Seung Hyuk BAIK ; Kyung Suk LEE ; Seung Yong JEONG ; Young Kyu PARK ; Hong Soo KIM ; Dong Ho LEE ; Han Jin OH ; Byung Chun KIM
Journal of Korean Medical Science 2009;24(Suppl 2):S271-S276
A systematic and effective welfare system for people with digestive system impairments is required. In Korea, an objective and scientific rating guideline does not exist to judge the digestive system impairments. Whether the impairments exist or not and the degree of it need to be examined. Thus, with these considerations we need a scientific rating guideline for digestive system impairments to fit our cultural and social background. In 2007, a research team, for the development of rating impairment guidelines, was organized under the supervision of Korean Academy of Medical Sciences. The rating guidelines for digestive system impairments was classified into upper and lower gastrointestinal tracts impairments and liver impairment. We developed objective rating guidelines for the upper gastrointestinal tract, the impairment generated after surgery for the stomach, duodenum, esophagus, and for the lower gastrointestinal tract, the impairment generated after construction and surgery for colon, rectum, anus, and intestinal stomas. We tried to make the rating impairment guidelines to include science, objectivity, convenience, rationality, and actuality. We especially emphasized objectivity as the most important value. We worked to make it easy and convenient to use for both the subjects who received the impairment ratings and the doctors who will give the ratings.
Digestive System Diseases/classification/*diagnosis
;
*Disability Evaluation
;
Duodenal Diseases/classification/diagnosis
;
Esophageal Diseases/classification/diagnosis
;
Humans
;
Inflammatory Bowel Diseases/classification/diagnosis
;
Korea
;
Liver Diseases/classification/diagnosis
;
Postoperative Complications/classification/diagnosis
;
Program Development
;
Severity of Illness Index
;
Stomach Diseases/classification/diagnosis