• 대한관절경학회지
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• 제7권1호
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• pp.87-91
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• 2003

건막 거대세포종은 관절내에 드물게 발생하는 병변으로 이를 보고하는 문헌도 제한되어 있으며 특히 후방십자인 대에 발생한 거대세포종의 국내 보고는 없었다. 저자들은 슬관절 후방십자인대에 발생한 거대세포종 2례를 관절경하에서 절제 후 병리학적으로 확진 하였으며 임상적으로 좋은 결과를 보였기에 문헌고찰과 항께 보고하고자 한다.

• 동의신경정신과학회지
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• 제15권1호
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• pp.127-141
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• 2004

This is 63 cases report of neurotic patient which have gone to Dep. of Neuropsychiatry of Dongshin University sunchun oriental hospital from October, 2002 to October, 2003. Objective : To find out distributional characteristics of neurotic patient Result : 1. The distribution of sex is Female and of age is thirty, fourty is large. 2. The distribution of a history of case is chronic patient is large. 3. The distributional ratio of psychosomatic : musculoskeletal : gastrointestine symptom of chief complain was 48.7: 25.3: 14.9. 4. The distribution of yanghyulansin ondam: soganhaewul gudam : bohyulansin description was 41.3: 15.9: 9.5. Conclusion : This 63 cases report is relatively small cases about analysis and comparison of neurotic patient. So, it's needed to abundant study of this, afterwards.

• Journal of Korean Neurosurgical Society
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• 제38권6호
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• pp.465-467
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• 2005

Anterior cerebral artery[ACA] dissecting aneurysms are extremely rare and optimal treatment remains unclear. The majority of cases manifest as cerebral infarction or as intracranial bleeding. The authors report two cases of ACA dissecting aneurysm, one with a large partially thrombosed gradually growing aneurysm and one with a cerebral infarction in the ACA territory. The patient with a large aneurysm was treated by trapping the aneurysm, and the patient with infarction by conservative management. We report on two cases of dissecting aneurysm of the ACA and include a review of pertinent literature.

• Journal of Chest Surgery
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• 제25권6호
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• pp.573-576
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• 1992

The pulmonary carcinosarcoma is a rare malignant tumor, which composed of an admixture of histologically malignant epithelial and mesenchymal tissues. Carcinosarcomas comprise 0.2% of all pulmonary neoplasms and are most often found in a proximal bronchus. We report two cases of the pulmonary carcinosarcoma with a rewiew of the literatures.

• Journal of Chest Surgery
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• 제5권1호
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• pp.41-44
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• 1972

Thymic cyst is a relatively uncommon,usually asymptomatic benign lesion situated in the anterior mediastinum or in the neck,and sometimes in both regions. This is a report of two cases of congenital thymlc cyst in a 18 year old girl and a 43 tear old man. Those were treated with extirpation of the cystic lesion by thoracotomy successfully and had good postoperative results.

• Journal of Chest Surgery
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• 제18권4호
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• pp.844-848
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• 1985

Mediastinal tumors which are originated in mediastinum or probably metastasized from other organs have long fascinated the surgeon because of difficulty of diagnosis and treatment. This report is the analysis of the 26 cases of mediastinal tumors, experienced in the Department of the Thoracic and Cardiovascular Surgery, Chosun University Hospital from January 1978 to January 1985. The result are as follows; 1. The age distribution was 10 months to 68 years old and the average mean age was 34.7 years old. 2. Subjective symptom were as follows: Dyspnea [69.2%], Coughing [42.3%], Chest pain [30.8%], Back pain [15.4%] and Numbness of extremities [15.4%]. Objective signs were as follows: Decreased breathing sound [53.3%], Pleural effusion and hemothorax [34.6%], Palpable neck mass [34.6%], SVC Syndrome [19.4%] and Bloody sputum [15.4%]. But, there were no definitive symptoms in 2 cases. 3. The malignant tumors were 19 cases [73.1%]. 4. The germ cell tumors were 2 cases [7.7%], the neurogenic tumor were 3 cases [11.5%], lymphoma were 8 cases [30.8%], thymoma were 2 cases [7.7%], mesenchymal tumor was 1 case [3.8%], cyst was 1 case [3.8%] and carcinoma were 5 cases [19.2%] among the 23 cases, histologically analyzed. 5. The successful complete removal was done in 5 cases among 7 cases of benign tumors. In malignant cases, the surgical removal had been 7 cases and inoperable cases were treated to radiation and chemotherapy.

• Journal of Chest Surgery
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• 제32권10호
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• pp.962-965
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• 1999

Carcinosarcoma of the esophagus have an interesting pathologic feature of admixture of carcinomatous and sarcomatous lesion and accounts for 0.5∼1.5% of all esophageal neoplasm. Generally, it has been reported that these have better prognosis than the squamous cell carcinoma. We have experienced two cases of carcinosarcoma occurring at the mid-esophagus. In both two cases, Ivor Lewis operation was performed and lymph node metastasis was absent. The pathologic diagnosis was confirmed as carcinosarcoma. Postoperative course was uneventful and the patients have been followed up for 3 months and 3 years, respectively, without any problems. We report these cases with a brief review of the literatures.

• Journal of Chest Surgery
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• 제16권3호
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• pp.391-398
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• 1983

This is a report of 6 cases of esophageal diverticulum at the mid-thoracic esophagus treated surgically at the Department of Thoracic and Cardiovascular Surgery, Hanyang University Hospital during the 10 years. Five patients were female and one was male and the age distribution was between 31 and 61 years, Various subjective symptoms were noticed preoperatively. Diagnosis was confirmed by esophagography. The type of esophageal diverticulum were pulsion type in five cases and traction type in one case. After diverticulectomy, subjective symptoms disappeared and there were no operative complications and mortality. Recurrence of symptoms was not noticed during follow-up.

• Journal of Chest Surgery
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• 제5권2호
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• pp.147-152
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• 1972

This is a report on the 4 cases of benign mediastinal teratoid tumor in the Department of Thoracic Surgery Chonnam University Hospital during the period from August, 1961 to August ,1972. All the tumors were teratomas which had three germinal layers and located in the anterior mediastinum. All the cases had symptoms such as Pancoast syndrome. exertional dyspnea, middle lobe syndrome with fistulous Connection to the cyst and retrosternal discomfort. X-ray studies are essential to recognize the tumor and its location. It`s believed that a exploratory thoracotomy is recommended because of the complications of the tumors and a possibility of malignancy.

• Journal of Chest Surgery
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• 제27권8호
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• pp.700-704
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• 1994

Congenital coronary arteriovenous fistula is relatively rare congenital heart disease which has formation of fistula between coronary artery and cardiac ventricle, atrium, or pulmonary artery, but that can be repaired with simple surgical procedure. We experienced three cases of congenital coronary arteriovenous fistula, which were repaired surgically under cardiopulmonary bypass, so we report these cases with review of the literatures.