• Proceedings of the KOR-BRONCHOESO Conference
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• 2001.12a
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• pp.29-30
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• 2001

• Journal of Chest Surgery
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• v.18 no.3
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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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• v.16 no.1
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• pp.146-152
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• 1983

Hamartoma has been considered rare disease as a congenital malformation of a tumorous lesion since the original description by Albrecht in 1904. Pulmonary hamartoma is interesting to chest surgeon because of good result by surgical procedures and of slightly high incidence then another organs. It is characterized as lesion of very slow growing mass as peak incidence of age of 50 years age group and as sex ratio is 2:1. Especially endobronchial hamartoma is rarer than peripheral type. We had experienced a case of endobronchial hamartoma who has 53 years old male patient at right main bronchus and then treated by excision of tumor mass through right bronchotomy and preserving right lung except any lobectomy and pneumonectomy.

• Journal of Chest Surgery
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• v.2 no.1
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• pp.19-24
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• 1969

A bronchial adenoma. being one of rare neoplastic diseases in children, was reported in a 4 year-old-male child. The tumor was located entirely intraluminal in the left main bronchus and was treated with left pneumonectomy because of the irreversible cystic changes were revealed throughout the left lung on open thoracotomy. The tumor was histologically confirmed to be a muco-epidermoid type of bronchial adenoma.

• Journal of Chest Surgery
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• v.25 no.10
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• pp.1066-1069
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• 1992

The bronchogenic cyst is not so rare in incidence, but it is rare for this cyst to cause compression of trachea and main bronchi. A 6-year old female child was evaluated for coughing, fever and left total atelectasis. This patient had a history of frequent upper respiratory symptom like bronchial asthma since 6month after birth. Fiberoptic bronchoscopy revealed external compression at distal trachea and both main bronchi. Computed Tomography revealed well demarcated homogeneous mass compressing distal trachea and main bronchi. The pathological examination showed bronchogenic cyst and this patient had uneventful recovery.

• Journal of Chest Surgery
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• v.28 no.4
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• pp.423-425
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• 1995

Endobronchial hamartoma is a extremely rare lesion. The patient was 47 years old female and complained of cough and dyspnea for several years. On bronchoscopy, a finger tip size mass, nearly occluding the left main bronchus and located 4cm from the carina, was found. Bronchoscopic biopsy showed the chronic inflammatory findings.We performed bronchotomy and removed the mass through left thoracotomy. The endobronchial tumor was confirmed hamartoma histopathologically.

• Journal of Chest Surgery
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• v.19 no.4
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• pp.731-735
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• 1986

Atelectasis with chronic pneumonitis affecting the right middle lobe secondary to compression of the middle lobe bronchus by enlarged indurated or calcified peribronchial nodes is defined as middle lobe syndrome clinicopathologically. The lesion in this series of case reports including tuberculous lymphadenitis, lung cancer, atelectasis and lung abscess with organizing pneumonitis, had been treated by lobectomy. Postoperative courses were uneventful in all patients. Herewith, we report these four experiences with review of literature.

• Journal of Chest Surgery
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• v.33 no.4
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• pp.324-328
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• 2000

Multiple primary lung cancer is not common and classified as a synchronous primary lung cancer and a metachronous primary lung cancer. We experienced one case of the triple synchronous primary lung cancer of different cell types. We conducted right pneumonectomy for preoperative diagnosed neuronendocrine tumor of the RUL and adenocarcinoma of the RLL. Pathologic examination revealed the carcinoid tumor of RUL bronchus, the squamous carcinoma of the RML and the adenocarcinoma of the RLL.

• Journal of Chest Surgery
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• v.19 no.3
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• pp.433-437
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• 1986

Authors experienced a case of typical carcinoid in a patient of 46 year-old female who has been suffered from hemoptysis intermittently for 13 years. Exploratory thoracotomy and middle and lower lobectomy was carried out. The tumor was located in the right intermediate bronchus. Tissue pathology shows a glandular tumor with focal proliferation of Kulchitzky cells in the bronchial epithelium by H&E stain and membrane-bounded neurosecretory granules in the cytoplasm by electron microscope. Authors report the case with a literature reviews.

• Korean Journal of Bronchoesophagology
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• v.8 no.1
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• pp.66-70
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• 2002

In patient with lung cancer, the resection margin of right main bronchus was invaded by tumor intraoperatively. So we performed tracheal reconstruction with autologous pericardium after resection of lower trachea including carina. Postoperatively, the patient discharged well and followed up for 5 months without any evidence of tumor recurrence or restenosis.