• Tuberculosis and Respiratory Diseases
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• 제45권1호
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• pp.234-237
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• 1998

A 64-year-old male was admitted due to weight loss of 5kg during a month. Chest X-ray showed two large, lobulated masses on both lower lobe. Chest CT showed ill-defined, multilobulated mass on left lower lobe and irregular, relatively homogenous mass with air-bronchogram on right lower lobe. Left lower lobectomy and right lower lobectomy was performed sequentially with three months interval. Microscopic findings showed squamous cell carcinoma of both mass. It was thought that this patient had synchronous double primary lung cancer.

• Journal of Chest Surgery
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• 제15권1호
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• pp.15-20
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• 1982

During the past ten years from 1972 to 1981, a total of 100 cases of bronchiectasis were treated by pulmonary resection at C.A.F.G.H. Pulmonary tuberculosis and frequent U.R.I. were the most frequent associated disease and encountered in 54% in this series. Various types of pulmonary resection were performed on 100 patients; left lower lobectomy in 40 cases, left lower lobectomy and lingular segmentectomy In 29 cases, right lower lobectomy in 12 cases, right middle and lower lobectomy in 12 cases, lingular segmentectomy in 3 cases, left pneumonectomy in 3 cases and both lower lobectomy in 1 case. Complications developed in 9 cases and 1 case among them died of sepsis following secondary opera-tion. Among complications of 9 cases, postoperative atelectasis showed in 4 cases, hemorrhage in 2 cases, bronchopleural fistula in 2 cases, pulmonary edema in 1 case. Complications were treated by conservative and secondary operative management with satisfactory result except one death. Remainders without complication showed good result without symptom in postoperative and follow-up periods.

• Journal of Chest Surgery
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• 제12권3호
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• pp.159-164
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• 1979

Kartagener`s syndrome is a clinical entity comprising a combination of situs inversus, bronchiectasis, and sinusitis or nasal polyposis. This syndrome is rare and is usually seen in a young age group. The syndrome is punctated by recurrent upper respiratory tract infection and pneumonia. This is a report of Kartagener`s syndrome found in 18 years old male and 21 years old female patients who were received surgical treatment of bronchiectasis. The male patient was performed right transposed lingular segmentectomy and lower lobectomy and female patient was perforated left transposed middle lobectomy and lower lobectomy. Both patients were discharged with good results.

• 한국임상수의학회지
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• 제30권6호
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• pp.409-414
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• 2013

본 연구에서는 개에서 일반 개흉술을 통한 폐엽절제술과 흉강경을 이용한 폐엽절제술에서 심폐기능 및 생체 내 산화스트레스 상태에 미치는 영향을 비교 연구 하였다. 10 마리의 건강한 혼혈종을 사용하였고 일반 개흉술을 통한 폐엽절제술군 (group 1, n=5)과 흉강경을 이용한 폐엽절제술군 (group 2, n=5)으로 분류하였다. 심혈관계 측정 항목 및 superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx)의 농도를 측정하였다. 두 군에서 동맥혈액 가스의 유의적인 변화를 관찰 할 수 있었다. 총 마취 및 수술 시간은 개흉수술군에 비해 흉강경 폐엽 절제술군에서 유의하게 짧았다. 혈장 SOD와 CAT 수준의 증가, 그리고 GPX 수준의 감소는 수술 후 두 군 모두에서 관찰되었다. 두 군을 비교했을 때 GPX 수준에서 유의한 차이가 발견되었다. GPX 수준은 개흉 수술 군과 비교 흉강경 폐엽 절제술 군에서 유의하게 낮았다.

• Journal of Chest Surgery
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• 제30권2호
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• pp.226-230
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• 1997

본 증례는 잦은 상기도 감염을 보였던 마제상폐를 동반한 양측성 엽내형 폐격리증의 성공적 치료에 대한 보고이다. 단순 흉부X-선상 양측 폐하엽 에 폐렴정 경화와 침윤을 보였으며 흉부전산화단층촬영상 폐격리증에 합당한 다발성 낭성병변을 보였다. 대동맥조영술에서 횡격막 상부에서 시작되어 양측 격리 폐로 유입되는 2개의 기 형체동맥을 관찰할 수 있었다. 좌측 개흉술을 통하여 좌측과 우측의 격리폐로 유입되는 체동맥을 결찰후 분리하고 좌하엽의 폐엽절제술을 시행한 다음 마제상폐의 협소부를 분리절 제후 우측 격리폐는 남겨두었다. 환자는 수술후 10일째 퇴원하였으며 잔류 우측 곁리폐의 합병증이나 증상없이 추적관찰중이다. 수술후 5개월깨 시행한 흉부전산화단층촬영상 남겨두었던 잔류 우측 격 리폐 는 자연 소실되었음을 관찰할수 있었다 본 증례로 보아 합병증이 없는 엽내형 격리폐에서 폐엽절제술 을 시행하지 않고 기형체동맥을 결찰분리만하는 새로운 치료방법을 제안해 보는 바이다.

• Journal of Chest Surgery
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• 제18권3호
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• pp.487-491
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• 1985

Two cases of plasma cell granuloma of the lung, whose incidence is 0.7% in the tumor of the lung and bronchus, are managed at department of thoracic and cardiovascular surgery, College of Medicine, Choong Nam national University Hospital from March, 1983 to July, 1984. The plasma cell granuloma of the lung, which is usually asymptomatic, is most commonly detected in routine chest films. The prognosis of the plasma cell granuloma is good after surgical resection. One case [female] was undertaken right pneumonectomy, the other, left lower lobectomy. Both cases had uneventful postoperative courses and are well being now.

• Journal of Chest Surgery
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• 제20권3호
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• pp.578-581
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• 1987

A very rare form of intrapulmonary cyst is an enterogenous cyst two examples of which were described by Ward and Krahl [1942]. Microscopically, the cyst wall is lined by gastric or intestinal type of mucous membrane which may include islets of pancreatic tissue; their walls contain muscle but no cartilage. We recently experienced a case of intrapulmonary enterogenous cyst. The patient was 30-year-old-male who showed chest pain and tightness after chest trauma. Chest X-ray revealed pneumothorax in both lung field with giant bullae in left upper lung field, right 6th and 7th rib fracture. Left lower lobectomy including cyst was done and the postoperative course was uneventful.

• Journal of Chest Surgery
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• 제22권3호
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• pp.498-502
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• 1989

Carcinosarcoma is the group of neoplasms possessing both carcinomatous parenchyma and sarcomatous stroma. These tumors are relatively uncommon and may arise in variable organs. In this case, a 62-year-old male patient was admitted to our department due to left chest pain and general weakness of three months duration. The chest x-ray revealed egg-sized, relatively well defined lobulated soft tissue mass in left paracardiac area. Left lower lobectomy was performed under the preoperative impression of lung cancer. Pathologic examination of the resected lung revealed carcinosarcoma without regional lymph node metastasis. Patient is doing well at present without any chemotherapy.

• Journal of Chest Surgery
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• 제46권6호
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• pp.475-477
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• 2013

In this article, we report a rare case of a 22-year-old male with bilateral pulmonary sequestration, treated with embolization and surgical resection. The initial plan involved staged bilateral lobectomy for both lungs and prophylactic embolization of feeding vessels for preventing unexpected hemorrhage during operation. Symptomatic right lower lobe was resected with video-assisted thoracic surgery after embolization, and the patient refused surgery of left lower lobe upon symptomatic relief. The two-year follow-up examination revealed that the patient was healthy and had no relevant discomfort.

• Journal of Chest Surgery
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• 제28권8호
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• pp.792-796
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• 1995

The pulmonary sequestration is a rare congenital malformation of the lung, concerning about the abnormal feeding systemic artery, may happen a serious complication of bleeding during operation if not recognized before operation. We experienced a case of bilateral intralobar pulmonary sequestration preoperatively confirmed by aortogram. An Aortogram demonstrated a anomalous systemic artery arising from thoracic aorta just above the diaphragm. The artery bifurcated and supplied areas of both right and left lower lobes. On the operative field, left lower lobectomy was done with devision and ligation of left branch of anomalous artery and triple ligation of remained branch of anomalous artery was done. Postoperative course was uneventful. She was discharged on postoperative seventeenth day.