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1.
The Korean Journal of Gastroenterology ; : 229-235, 2015.
Article in English | WPRIM | ID: wpr-194206

ABSTRACT

BACKGROUND/AIMS: Hepatic angiosarcoma, a rare and aggressive liver malignancy, is difficult to diagnose because of a lack of specific clinical features. The clinical and radiological features of patients with histologically confirmed hepatic angiosarcoma were examined. METHODS: Among 2,336 patients diagnosed with primary hepatic carcinoma at Keimyung University Dongsan Medical Center (Daegu, Korea) between May 2002 and February 2012, eight (0.03%) with histologically confirmed primary hepatic angiosarcoma were included. The patterns of disease diagnosis, tumor characteristics, treatment responses, and prognoses were reviewed retrospectively. RESULTS: Median age was 66 years-old (range, 41-80 years). Four patients were male. Five patients were compulsive drinkers. All patients had no HBsAg and anti-HCV. Initial radiologic diagnoses revealed primary hepatic angiosarcoma (n=2), hepatocellular carcinoma (n=2), hemangioma (n=2), and hepatic metastatic carcinoma (n=2). Definitive diagnoses were made by percutaneous needle biopsies in seven patients and surgical resection in one patient. At the time of the initial diagnosis, extrahepatic metastases were detected in three patients (37.5%). Metastatic sites included the spleen and lung, pericardium, and bone, in one patient each. Two patients underwent conservative treatments. The remaining patients underwent surgical resection (n=1), transcatheter arterial chemoembolization (n=1), and systemic chemotherapy (n=4). The median survival period was 214 days (range, 21-431 days). CONCLUSIONS: Hepatic angiosarcoma is a highly progressive disease with a poor prognosis. Detailed studies including histological examinations are essential to facilitate early diagnosis of the disease.


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Antineoplastic Agents/therapeutic use , Embolization, Therapeutic , Hemangiosarcoma/diagnosis , Immunohistochemistry , Liver Neoplasms/diagnosis , Neoplasm Metastasis , Prognosis , Retrospective Studies , Survival Rate , Tomography, X-Ray Computed
2.
The Korean Journal of Gastroenterology ; : 441-444, 2012.
Article in English | WPRIM | ID: wpr-155641

ABSTRACT

Sweet's syndrome (SS), also known as acute febrile neutrophilic dermatosis, is characterized by the sudden onset of painful erythematous skin lesions together with fever and neutrophilia. SS can be associated with several disorders, such as malignancy, autoimmune disease, and infections. However, SS associated with liver cirrhosis is uncommon. We report a case of SS in a patient who was diagnosed with liver cirrhosis caused by chronic hepatitis B.


Subject(s)
Humans , Male , Middle Aged , Hepatitis B, Chronic/complications , Liver Cirrhosis/diagnosis , Neutrophils/immunology , Skin Diseases/diagnosis , Sweet Syndrome/diagnosis , Tomography Scanners, X-Ray Computed
3.
The Korean Journal of Hepatology ; : 157-163, 2005.
Article in Korean | WPRIM | ID: wpr-19442

ABSTRACT

BACKGROUND/AIMS: Transjugular Intrahepatic Portosystemic Shunt (TIPS) is commonly used in patients with variceal bleeding. However, this procedure is contraindicated in hepatocellular carcinoma patients with portal vein thrombosis. This study was done to evaluate the effect of TIPS in those patients with variceal bleeding. METHODS: Between 1997 and 2004, six hepatocellular carcinoma (HCC) patients with portal vein thrombosis were enrolled in this study due to their variceal bleeding. All the patients underwent TIPS placement to treat the variceal bleeding that had not responded to endoscopic treatment. Effective shunt creation was assessed by the decrease of the portal pressure gradient (less than 12 mmHg) or if good patency and flow were seen on a doppler examination. RESULTS: Shunts were successfully created in all the patients and the bleeding was immediately controlled in the active bleeding cases. The bleeding was caused by esophageal varices in one patient and, by gastric varices in five patients. The HCC types were diffuse or massive in five patients, and a single nodule was present in one patient. All the patients had portal vein thrombosis. Rebleeding was noted in two patients at 10 days and 3 months, respectively, due to the shunt occlusion. Hepatic encephalopathy was noted in two patients. The causes of death were hepatorenal syndrome after 2 weeks in one patient, bleeding due to portal hypertensive gastropathy after 3 weeks in another, and cancer progression after 4 months in third patient. CONCLUSIONS: For HCC patients with portal vein thrombosis, TIPS can be an effective treatment modality if uncontrolled variceal bleeding presents when using endoscopic hemostasis or pharmacologic therapy. However, further studies are needed.


Subject(s)
Adult , Humans , Male , Middle Aged , Carcinoma, Hepatocellular/complications , English Abstract , Esophageal and Gastric Varices/complications , Gastrointestinal Hemorrhage/therapy , Liver Neoplasms/complications , Portal Vein , Portasystemic Shunt, Transjugular Intrahepatic , Venous Thrombosis/complications
4.
Korean Journal of Gastrointestinal Endoscopy ; : 131-135, 2004.
Article in Korean | WPRIM | ID: wpr-34273

ABSTRACT

Intestinal hemorrhage, fistula formation, and intestinal obstruction are the common complications associated with intestinal tuberculosis. However, duodenal fistula due to intestinal tuberculosis is very rare. We experienced a case of 26-year-old woman with a fistula in the duodenum referred to our hospital due to abdominal pain. Esophagogastroduodenoscopy showed a fistula at the duodenum with lymph node. After 2 months of anti-tuberculous medication, abdominal pain was improved and fistula size decreased. We report a case of fistula caused by duodenal tuberculosis.


Subject(s)
Adult , Female , Humans , Abdominal Pain , Duodenum , Endoscopy, Digestive System , Fistula , Hemorrhage , Intestinal Obstruction , Lymph Nodes , Tuberculosis
5.
Korean Journal of Gastrointestinal Endoscopy ; : 895-899, 1998.
Article in Korean | WPRIM | ID: wpr-198481

ABSTRACT

Menetrier's disease is a rare, characterized by the presence of large rugal folds involving part or all of the stomach. Patients with hypertrophic gastropathy often have distressing abdominal symptoms, weight loss, and edema due to gastric protem loss. A 64 year old male patient was admitted with the chief complaint of epigastric discomfort. Endoscopic, radiologic and histologic examination, revealed characteristic findings of Menetrier's disease. A case of Menetrier's disease is reported with a brief review of literature.


Subject(s)
Humans , Male , Middle Aged , Edema , Gastritis, Hypertrophic , Stomach , Weight Loss
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