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1.
J Viral Hepat ; 10(4): 241-8, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12823589

ABSTRACT

Hepatitis C virus (HCV) infection is the most common cause of chronic hepatitis, which frequently progresses to hepatocellular carcinoma. The pathogenesis of its persistent infection and tumour progression has not been fully characterized yet. The RCK gene was previously cloned at the breakpoint of the t(11;14)(q23;q32) chromosome translocation observed in human B-cell lymphoma cell line RC-K8. The RCK protein, rck/p54, which is a 54-kDa cytoplasmic protein belonging to the DEAD box/RNA helicase family, is considered to facilitate the translation of mRNA(s) of genes for cell proliferation and malignant transformation not only in B-cell lymphomas having the t(11;14) translocation but also in other solid tumours. The aim of this work was to examine the involvement of rck/p54 in carcinogenesis of hepatocellular carcinoma from HCV-related chronic hepatitis. We examined the expression of rck/p54 in 29 cases of HCV-related chronic hepatitis and eight cases of hepatocellular carcinoma by immunohistochemistry and Western blot analysis. Twenty-six of 29 cases with HCV-related chronic hepatitis and all cases with hepatocellular carcinoma tested overexpressed rck/p54 protein. The expression of rck/p54 was lowered by treatment with IFN-alpha in two cases who showed the decrease in HCV RNA levels. These findings suggest that rck/p54 protein is possibly involved in the replication of HCV genomes in hepatocytes and in tumourigenesis of hepatocellular carcinomas.


Subject(s)
Carcinoma, Hepatocellular/genetics , Cell Transformation, Neoplastic/pathology , Genetic Predisposition to Disease , Hepatitis C, Chronic/genetics , Liver Neoplasms/genetics , Proto-Oncogene Proteins/genetics , RNA Nucleotidyltransferases/genetics , Adult , Aged , Biopsy, Needle , Blotting, Western , Carcinoma, Hepatocellular/pathology , Cohort Studies , DEAD-box RNA Helicases , Female , Gene Expression Regulation, Neoplastic , Genome , Hepatitis C, Chronic/pathology , Hepatocytes/pathology , Humans , Immunohistochemistry , Liver Neoplasms/pathology , Male , Middle Aged , RNA Helicases/genetics , Reverse Transcriptase Polymerase Chain Reaction , Sensitivity and Specificity
2.
Am J Gastroenterol ; 94(3): 643-9, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10086645

ABSTRACT

OBJECTIVE: Balloon-occluded retrograde transvenous obliteration is an effective new method for treating gastric fundal varices, but subsequent occurrence of esophageal varices creates a problem. The relationship between portal hemodynamics and the occurrence of esophageal varices after prophylactic balloon-occluded retrograde transvenous obliteration was investigated. METHODS: Ten cirrhotic patients considered to have high risk gastric fundal varices underwent angiography. Six patients showed a communication between blood flow in gastric wall vessels and that in the gastrorenal shunt (type I), whereas the others (type II) did not. Depending on the flow direction in the left gastric vein, the two groups were further divided into hepatopetal (a) and hepatofugal (b) subgroups. The therapeutic effect on portal hemodynamics and the relationship between pretreatment portal hemodynamics and posttreatment occurrence of esophageal varices were investigated. RESULTS: Fundal varices disappeared endoscopically in all 10 patients and the gastrorenal shunt was also occluded after the procedure. No patient showed worsening of liver function or systemic complications during follow-up. The increase in portal blood flow was more significant in type Ib patients than in the others. Esophageal varices occurred in all type I patients, and as to those in type Ib, high risk varices developed within 6 months after treatment. On the other hand, esophageal varices did not occur in type II patients. CONCLUSIONS: This procedure was effective for treating gastric fundal varices. However, type Ib patients are likely to develop high risk esophageal varices after occlusion of the gastrorenal shunt.


Subject(s)
Catheterization , Esophageal and Gastric Varices/therapy , Sclerotherapy/methods , Adult , Aged , Aged, 80 and over , Blood Flow Velocity , Esophageal and Gastric Varices/complications , Esophageal and Gastric Varices/diagnostic imaging , Esophageal and Gastric Varices/physiopathology , Female , Humans , Liver Circulation , Liver Cirrhosis/complications , Male , Middle Aged , Portal Vein/physiopathology , Risk Factors , Stomach/blood supply , Ultrasonography, Doppler
3.
Gastrointest Endosc ; 45(6): 498-502, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9199908

ABSTRACT

BACKGROUND: A prospective randomized controlled study was performed to evaluate the usefulness of prophylactic endoscopic sclerotherapy in patients with hepatocellular carcinoma complicated by esophageal varices. METHODS: The subjects included 58 patients with esophageal varices negative for the red color sign and hepatocellular carcinoma without tumor emboli in the portal trunk or primary portal branches. Patients were randomly assigned to prophylactic sclerotherapy (n = 29) or control (n = 29) groups, and their bleeding and survival rates were compared. RESULTS: A mean of 3.0 sclerotherapy sessions was required for complete disappearance of varices in patients receiving prophylactic sclerotherapy. During the observation period, transcatheter arterial embolization for hepatocellular carcinoma was performed more often in patients with prophylactic sclerotherapy (mean 3.8 times) than in control patients (mean 2.0 times) (p < .05). Percutaneous ethanol injection therapy was performed more often in patients with prophylactic sclerotherapy than in controls (mean 8.1 times vs 5.0 times, respectively) (p < .05). The 3-year bleeding rates were 50% for the control group and 18% for the prophylactic sclerotherapy group (p < 0.05), and the 3-year survival rates were 16% for the control group and 37% for the therapy group (p < 0.05). CONCLUSIONS: Prophylactic sclerotherapy improves survival in patients with hepatocellular carcinoma complicated by red color sign-negative esophageal varices without tumor emboli in the portal trunk or primary portal branches.


Subject(s)
Carcinoma, Hepatocellular/complications , Esophageal and Gastric Varices/prevention & control , Gastrointestinal Hemorrhage/prevention & control , Liver Neoplasms/complications , Sclerotherapy/methods , Adult , Aged , Carcinoma, Hepatocellular/diagnosis , Carcinoma, Hepatocellular/therapy , Cause of Death , Color , Embolization, Therapeutic , Endoscopy, Digestive System/methods , Esophageal and Gastric Varices/complications , Esophageal and Gastric Varices/mortality , Follow-Up Studies , Gastrointestinal Hemorrhage/etiology , Gastrointestinal Hemorrhage/mortality , Hepatectomy , Humans , Liver Neoplasms/diagnosis , Liver Neoplasms/therapy , Middle Aged , Portography , Prospective Studies , Survival Rate , Treatment Outcome
4.
J Cutan Pathol ; 23(6): 566-70, 1996 Dec.
Article in English | MEDLINE | ID: mdl-9001989

ABSTRACT

An autopsy case of malignant eccrine poroma (MEP) with multiple visceral metastases is reported. A flat, dark tumor of 1 cm in diameter developed on a pre-existing pigmented spot at the left side of the waist of a 58-year-old male. The histopathology suggested the tumor to be malignant melanoma. Nine years later, a painless swelling occurred in the left lower leg, resulting from the obstruction of lymphatics at the left inguinal region. The swelling continued and spread with pain, reaching the inguinal region. Two years later, several papules appeared around the left knee, from which an extensive lymphorrhea occurred. The histopathology of the resected papules suggested epidermoid carcinoma or trichilemmal carcinoma, mainly localized within the lymphatics of the upper dermis. Re-examination of the first skin tumor and electron microscopy of the tumor obtained at autopsy revealed that both tumors were MEP. Although the metastases to the local cutaneous regions and lymph nodes via the lymphatics occur in 20% of MEP, cases with multiple visceral metastases are very few.


Subject(s)
Acrospiroma/pathology , Sweat Gland Neoplasms/pathology , Autopsy , Diagnosis, Differential , Humans , Male , Middle Aged , Neoplasm Metastasis , Viscera/pathology
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