• Journal of Chest Surgery
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• 제23권6호
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• pp.1270-1274
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• 1990

In mediastinum, teratoma frequently occur in anterior mediastinal compartment. Rarely discovered in pericardium, posterior mediastinum and lung parenchyme. The incidence of posterior mediastinal teratoma was 3%~8%. A young male patient was treated with posterior mediastinal teratoma. So we describe the rare disease.

• Journal of Chest Surgery
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• 제33권6호
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• pp.521-524
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• 2000

The benign teratoma is usually slow growing tumor, but we expirienced a case of primary huge mediastinal benign teratoma that had grown very rapidly, maximally during 3 years. The 14-year-old female patient was admitted to our hospital because of abnormal chest X-ray that showed 10$\times$10cm sized well definded mass with multiple calcificactions. but the mass was not present in chest X-ray perfomed on 3 years prior to admission. Under the diagnosis of teratoma, complete surgical resection was done by the left thoracotomy. The result of pathology was benign teratoma.

• Journal of Chest Surgery
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• 제13권2호
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• pp.138-142
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• 1980

mediastinal teratomas are encountered commonly in adult life, and rarely in childhood. Characteristically, these mediastinal teratomas are located anteriorly with only rare examples in the posterior mediastinum. The cystic teratoma usually behaves as a benign neoplasm, but the solid [non-cystic] teratoma is frequently malignant. We experienced a case of large anterior mediastinal cystic teratoma in a two-years old boy, which was treated by complete surgical excision with good result.

• Journal of Chest Surgery
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• 제10권1호
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• pp.59-64
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• 1977

Mediastinal tumor are frequently encountered in clinical practice. Hanten, in 1955, reported-2 adult patients with spontaneous rupture of mediastinal dermoid cysts into the pleural cavity and also, Thompson, in 1963, reported 2 child patients with spontaneous rupture of mediastinal teratoma into the pleural cavity. Mediastinal teratomas have also been reported rupture into other contiguous structures, such as the bronchus, aorta, pericardium, SVC and esophagus. This report presents an instance of spontaneous rupture of an anterior mediastinal teratoma into the right pleural cavity of a 43 year old female. Despite variable diagnostic procedures, the true nature of the lesion was not determined until a thoracotomy and window formation was performed for adequate drainage of empyema thoracis. Removal of the teratoma and mediastinal window formation resulted in complete cure.

• Journal of Chest Surgery
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• 제46권4호
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• pp.305-308
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• 2013

We report a rare case of rhabdomyosarcoma spontaneously arising in an anterior mediastinal teratoma in a 47-year-old male. The patient was found to have an anterior mediastinal mass on a chest X-ray, which was taken two months before his presentation to Asan Medical Center. A subsequent computed tomography scan revealed an $8.9{\times}7.1{\times}8.0$ cm heterogeneous mass in the anterior mediastinum. He underwent an excision via median sternotomy. The histopathologic study identified a mature teratoma with embryonal rhabdomyosarcoma.

• Journal of Chest Surgery
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• 제17권2호
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• pp.299-304
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• 1984

Tumors of the mediastinum are usually classified according to their location in the anterior, middle, or posterior mediastinum. Mediastinal teratomas are characteristically located at anterior mediastinum with only rare incidence in the posterior mediastinum. Two cases of posterior mediastinal teratoma were experienced recently, in the department of thoracic surgery, Seoul National University Hospital. The incidence of posterior mediastinal teratoma was 4.2% among 48 mediastinal teratomas in our experience. Two cases are all benign teratoma located at right posterior costophrenic angle, and histologically showed tissues from three germ layers including bone and fat.

• Journal of Chest Surgery
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• 제15권2호
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• pp.169-173
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• 1982

We have experienced two cases of complicated teratoma in anterior mediastinum. One case, 1-year-old female, has a huge anterior mediastinal teratoma involving almost all of the left pleural cavity with atelectasis of the left lung. The other case, 12-year-old female, has a anterior mediastinal teratoma with fistula between the teratoma and the bronchus of anteromedial basal segment of left lung. The bronchus has a bronchiectatic change with cell infiltration. We performed exploratory thoracotomy with complete excision of tumor mass in both cases and with additional resection of anteromedial basal segment of the left lung due to inflammation and necrosis in latter case. The patients had uneventful postoperative courses and were discharged in good condition. Histopathologic diagnosis of these were benign teratoma consist of skin, skin appendages, cartilage, connective tissue, and gut.

• Journal of Chest Surgery
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• 제28권6호
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• pp.644-648
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• 1995

Intrapulmonary teratoma is rare : only 30 cases have been reported in the world literature. We had experienced a case of benign intrapulmonary teratoma originated from anterior mediastinum associated with broncho-tumorous fistula, which was treated with En bloc removal of tumor and right middle lobectomy. Post-operative course was not eventful.

• Journal of Chest Surgery
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• 제39권9호
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• pp.729-732
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• 2006

외상에 의하여 심장눌림증을 유발한 종격동 양성낭기형종 종격동 기형종은 전체 종격동 종양의 $8\sim13%$ 빈도로 발생하며, 대부분 우연히 발견되지만 드물게 심낭 천공이 발생하여 심장눌림증을 유발하거나, 흉막삼출액을 고이게 한다. 본 증례에서는 전흉벽 타박상을 받은 여자 환자에게서 심장눌림증이 발생하였고, 응급 방사선검사에서 종격전부 종양이 확인되었으며 심장막천자술을 받은 후 활력징후가 회복되어 추후 수술적 절제술로 종양을 적출하였다. 조직검사에서 피지선, 성숙 지방종, 위장관점막, 호흡기도 점막 및 췌장의 조직 등으로 구성된 낭포성 구조물로 관찰되어 양성 낭기형종으로 판정되었다.

• Tuberculosis and Respiratory Diseases
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• 제47권3호
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• pp.400-405
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• 1999

저자들은 간헐적으로 객혈을 하였던 18세 여자 환자에서 종격동 기형종의 자연파열에 의해 발현될 수 있는 심낭삼출 및 흉막삼출, 폐렴, 객혈 등의 소견이 동시에 발현된 증례를 경험하였기에 문헌고찰과 함께 보고하는 바이다.