• Journal of Chest Surgery
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• v.15 no.3
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• pp.290-294
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• 1982

Diaphragmatic eventration is a rare disease, congenital or acquired, high or elevated position of one leaf of the diaphragm muscle, as a result of paralysis, aplasia or atrophy of varying degree of the muscle fibers of the affected side but with no break in the continuity of the muscle. We experienced 3 cases of the diaphragmetic eventration at the department of thoracic surgery, C.A.F.G.H., from 1980 to 1982, which were treated successfully. Among three cases, one case combinded with hamartoma of the ipsilateral lung. Specific complications were not noticed after surgical repair of diaphramatic eventration with good result.

• Journal of Korean Academy of Oral and Maxillofacial Radiology
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• v.27 no.1
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• pp.251-262
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• 1997

The authors reported 3 cases of cherubism which included easily diagnosable cases with typical clinical and radiologic features and a difficult case in which a through study of familial factor contributed to final correct diagnosis.

• Journal of Chest Surgery
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• v.25 no.11
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• pp.1221-1224
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• 1992

There is collected cases report of esophagus diverticulum treated at the dept. of Thoracic & Cariovascular surgery of Pusan National University Hospital during the past 13 years from 1980 to 1992. The total number were 6 cases. In consideration of their sites, the cervical esophageal diverticulum one, the mid-thoracic diverticulum were five. And their pathogenetic analysis revealed 5 in traction type, and 1 in pulsion type. The investigation and analysis have been done in comparision with current concept of esophageal diverticulum.

• Journal of Chest Surgery
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• v.25 no.11
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• pp.1265-1268
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• 1992

Primary tumors of the heart are extremely rare, and about 25 per cent of all primary cardiac tumors are malignant. Recently We experinced three cases of primary malignant tumor; malignant fibrous histiwytoma, carcinosarcoma, and synovial sarcoma, These three cases involved 2 men and 1 woman. There was one operative death, and two operative survivors died of metastatic disease at 12 months postoperatively in spite of chemotherapy and radiotherapy. We report these three cases of primary malignant cardiac tumors with review of the literatures.

• Journal of Chest Surgery
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• v.11 no.4
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• pp.476-480
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• 1978

Bronchogenic cysts are congenital and uncommon lesions which are derived from primitive forgut and usually found within the lung or mediastinum. The increased use of roentgenograms of the thorax and the widening scope of thoracic surgery, many more cases of bronchogenic cysts are being observed. Three cases of bronchogenic cysts operated in the department of thoracic surgery, C.A.F.G.H., are reported and the related literatures are reviewed.

• Journal of Chest Surgery
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• v.16 no.4
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• pp.518-525
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• 1983

Hydatid cystic disease of the lung is rare in Korea. Recently, the authors encountered 2 patients with this disease who were treated surgically with a successful outcome in both. The first patient, a 27 year old housewife never traveled outside Korea and the second, 25 year old man had a history of spending a year in Kuwait. These 2 cases are the first documented cases of pulmonary hydatoidosis among Koreans reported in the literature.

• Journal of Chest Surgery
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• v.21 no.1
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• pp.196-199
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• 1988

The bronchogenic cyst, one of rare congenital cystic disease, was reported occasionally since the first description of Bartholinus in 1678. The increased use of roentgenograms of the thorax and the widening scope of thoracic surgery was made, and much more cases of bronchogenic cysts has been observed. The most common location of a mediastinal bronchogenic cyst was the hilum. The treatment for bronchogenic cyst is surgical resection. Forty eight cases of bronchogenic cysts which were pathologically confirmed, are reported and the related literatures are reviewed.

• Journal of Chest Surgery
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• v.16 no.3
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• pp.381-385
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• 1983

Congenital bronchoesophageal fistula without esophageal atresia is very rare and often has an insidious clinical course that occasionally persists into adult life. Here are presented five cases of congenital bronchoesophageal fistula without esophageal atresia in adults treated successfully in the Seoul National University Hospital. The patients included two women and three men in the range of 16 and 45 years old. [mean age: 32 years old] Three of five cases could be diagnosed preoperatively by esophagogram and bronchogram but two of them could only be found in operative field. Cineesophagogram is recommended, on review of the literature, to be the most rewarding diagnostic procedure.

• Journal of Chest Surgery
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• v.14 no.4
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• pp.364-368
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• 1981

There is collected cases report of esophagus diverticulum .treated at the dept. of Thoracic & Cardiovascular surgery of National Medical Center During the past 21 years from 1960 to 1981 . The total number were l0 cases in consideration of their sites, the pharyngoesophageal diverticulum was only one, the cervical esophageal diverticulum one, the mid thoracic diverticulum were Six, and the epiphrenic diverticulum were two. And their pathogenetic analysis revealed 6 in traction type, and 4 in pulsion type. The investigation and analysis have been done in comparison with current concept of esophageal diverticulum.

• Journal of Chest Surgery
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• v.5 no.2
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• pp.141-146
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• 1972

The intrapulmonary teratoma is an extremely rare tumor. Since the orlginaI description by Black in 1981. about 19 cases have been reported in the would literature. We wish to describe the two cases of another patients with this extremely rare tumor.