No abstract available.
Fathers* ; Humans

No abstract available.
Teratoma*

No abstract available.
Diagnosis* ; Ultrasonography*

No abstract available.
Diagnosis* ; Ultrasonography*

The authors experienced a case of juvenile type cervical arteriovenous malformation. It was apoplectic in onset and represented spastic quadriparesis, sensory impairment and voiding difficulty. The authors treated with total excision of voluminous malformed vessels with good results.
Arteriovenous Malformations* ; Muscle Spasticity ; Quadriplegia

No abstract available.

No abstract available.
Nausea* ; Ondansetron* ; Vomiting*

Eleven cases of paragonimus brain abscess which were surgically treated from 1975 to 1978 were reviewed. All patients received supplementary bithionol therapy. Ten patient's clinical condition improved. Only one patient died due to post operative wound infections.
Bithionol ; Brain Abscess* ; Brain* ; Humans ; Paragonimus* ; Wound Infection

Budd-Chiari syndrome (BCS) is a rare disease caused by the obstruction of the hepatic venous outflow or the inferior vena cava above the hepatic vein. It has been attributed to various etiologic factors. Including intrinsic vascular thrombosis, hepatic tumor invasion/compression, or associated with an idiopathic obstructing membrane. However, in most cases no definitive etiologic factors have been identified. Recently, we experienced a case of 21-year-old man who had Budd-Chiari syndrome associated with diaphragmatic hernia. Venous flow returned to normal on reintroduction of the liver into the abdominal cavity and closure of the defect in the diaphragm. To our knowledge, this is the rare report in our country. Here, we report this case with review of literatures.
Abdominal Cavity ; Budd-Chiari Syndrome* ; Diaphragm ; Hepatic Veins ; Hernia ; Hernia, Diaphragmatic* ; Humans ; Liver ; Membranes ; Rare Diseases ; Thrombosis ; Vena Cava, Inferior ; Young Adult

Liposarcoma is a mesenchymal malignant tumor which occurs most frequently in the limbs, retroperitoneum, and trunk: Although primary liposarcoma may occur anywhere adipose tissue is found, visceral locations are only rarely represented. Moreover, primary gastric liposarcoma is extremely rare. So, only a few cases of primary gastric liposarcoma have been reported in English literature. We describe the case of a 43-year-old woman presenting with melena, epigastric pain, general weakness. Esophagogastroduodenoscopy (EGD) showed a 6x4x3 cm sized-mass which was located on the posterior gastric wall. By endoscopic ultrasonography and abdominal CT scan, we suspected gastric lipoma and performed the laparoscopic transgastric tumor resection by eversion method. Finally, it was confirmed as a gastric liposarcoma pathologically. Herein, we present a case of gastric liposarcoma which was resected by laparoscopic transgastric wedge resection.
Adipose Tissue ; Adult ; Endoscopy, Digestive System ; Endosonography ; Extremities ; Female ; Humans ; Lipoma ; Liposarcoma* ; Melena ; Tomography, X-Ray Computed