• 제목/요약/키워드: Left main bronchus

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원발성 폐평활근육종 - 수술 치험 1례 - (Primary Pulmonary Leiomyosarcoma - A Case Report -)

  • 정태열;김태균;박문향;전석철
    • Journal of Chest Surgery
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    • 제33권7호
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    • pp.590-593
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    • 2000
  • 원발성 페평활근육종은 원발성 폐종양으로써 매우 드문 질환으로 대부분 기관지나 혈관들의 평활근에서 기시하나 드물게는 말초부에서도 생긴다고 한다. 이 드문 종양은 기관지종양과 유사하며, 국소적 혹은 전신적인 증상을 보인다고 하며, 관례적인 흉부방사선검사상 우연히 발견되기도 한다. 본원의 경우 61세의 남자환자에서 우연히 흉부방사선 검사상에 좌측 폐 말초부에서 발견된 큰 종괴가 발견되어 좌 전폐절제술을 시행하였으며, 이의 조직검사상 원발성 폐 평활근육종으로 술후 경과는 양호하였다.

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기관지성 낭종[3례 보고] (Bronchogenic Cyst: report of 3 cases)

  • 이종태;한승세;이성행
    • Journal of Chest Surgery
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    • 제14권3호
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    • pp.210-214
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    • 1981
  • The bronchogenic cysts result from an abnormal budding or branching of the tracheo-bronchial tree from the primitive foregut. Bronchogenic cysts may be pulmonary or mediastinal. The most common location for a mediastinal bronchogenic cyst is in relation to the carina. They are usually solitary. They usually are thin walled and contain fluid that is most often clear. The cyst is lined by ciliated columnar epithelium. The bronchogenic cyst i~ usually asymptomatic. They can cause pressure symptoms. When they become infected, symptoms do occur. We report 3 cases of bronchogenic cysts experienced at the Department of Thoracic and Cardiovascular Surgery, Kyungpook National University Hospital. Case I, a man of 20 year-old, had a cyst at the site between aortic arch and left pulmonary artery. He complained cough and dyspnea. The cyst wasn`t communicated with tracheobronchial tree. Case II was 55-year-old male who had had hemoptysis. A huge cyst was located within the lower lobe of left lung and removed by pulmonary lobectomy. There were not any symptoms in Case III that was 6-year old girl. That cyst was located just next to the right main bronchus.

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식도중간부 식도게실: 1 수술 치험례 (One case report of mid-thoracic esophageal diverticulum)

  • 선경;최영호;채성수;김학제;김형묵
    • Journal of Chest Surgery
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    • 제15권4호
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    • pp.447-450
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    • 1982
  • A 45 year old male officer was admitted due to upper substernal pain for 1 month, which was aggravated by swallowing. On past and family history, there was no specific history except heavy drinking. Simple chest x-ray revealed no specific abnormal findings. Preoperative esophagofiberscopy and Barium study showed midesophageal diverticulum, pulsion type, at about 2 cm below the left main bronchus. The opening of the diverticulum was located at the left posterolateral aspect of esophagus. Midesophageal false diverticulum, measuring 2 x 2 x 1 .S cm in size, was noted at about 5 cm under the aortic arch protruding through a slit-like muscular defect. After inversion of diverticular sac, interrupted sutures with 3-0 silks were done on muscular defect site, and mediastinal pleura was reinforced on the lesion with interrupted sutures. On 4th postoperative day, esophagography revealed no diverticulum or stenosis. Also esophagofiberscopy showed smooth mucosal tag without disturbance of passage. On 14th postoperative day, the patient was discharged uneventfully, and follow-up for 3 months after discharge revealed nothing abnormal symptoms. The authors report one case of midesophageal, pulsion type, false diverticulum.

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Sino-Bronchiectasis 에 대한 임상적 고찰 (Clinical and Pathological Study of Sino-bronchiectasis)

  • 김종원;서정회;최인환
    • Journal of Chest Surgery
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    • 제6권2호
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    • pp.151-158
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    • 1973
  • Author studied the pathogenesis of Sino-bronchiectasis with review of clincal and pathological findings of resected lungs in 24 eases of bronchiectasis,and the results were as follows: 1. Of the 24 eases of bronchiectasis, Sino-bronchiectasis were found in 11 cases and these cases most commonly, developed in first and second decade of life. In a majority of these cases,the main symptoms were the signs of wet bronchiectasis. 2. The typical roentgenograrn changes of plain chest x rays were increase in size and loss of definition of the markings and bronchographically revealed the cylindrical or tubular form in majority of these cases. 3. Pathologically Sino-bronchiectasis involved specific segmental areas of the lungs such as left basal and S4+5 segments and revealed commonly tubular dilatation. The most common findings of bronchial wall of dilated bronchus were the inflammatory cellular infiltration and cylindrical hyperplasia of mucus epithelial layers. 4. It was suspected that there were some causal relations in pathogenesis between chronic sinusitis and bronchiectasis.

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선양 낭포암에 의한 다발성 폐농양의 외과적 치료 - 1례 보고 - (Surgical Treatment of Multiple Lung Abscesses with Adenoid Cystic Carcinoma - A Case Report -)

  • 김도형;조현민;정은규;강두영;손국희;이두연
    • Journal of Chest Surgery
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    • 제35권1호
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    • pp.73-76
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    • 2002
  • 선양 낭포암은 종양의 진행 속도가 느리며 직접 국소 침범을 잘하는 종양이다. 종양의 특성 상 완전 종양 절제가 불가능한 경우 합병증을 해결하는 치료만으로도 장기간의 생존이 가능하다. 본 교실에서는 간에 전이된 선양 낭포암 환자에서 좌측 주기관지 폐쇄로 발생한 다발성 폐농양에 의한 악성 발열 증상을 좌측 전폐 절제술을 통해 치료하여 경과 양호하였기에 문헌고찰과 함께 보고하는 바이다.

Endobronchial Schwannoma Treated by Rigid Bronchoscopy with Argon Plasma Coagulation

  • Lee, Bo Ram;Choi, Yoo Duk;Kim, Yu Il;Lim, Sung Chul;Kwon, Yong Soo
    • Tuberculosis and Respiratory Diseases
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    • 제73권3호
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    • pp.174-177
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    • 2012
  • Primary endobronchial schwannomas are extremely rare tumors that originate from Schwann cells. We report a case of primary endobronchial schwannoma. A 44-year-old woman, without respiratory symptoms, was presented with a nodule in the left main bronchus on her chest computed tomography scan. The nodule was removed by a rigid bronchoscopy with argon plasma coagulation. Biopsy confirmed the diagnosis of schwannoma. There was no recurrence during her 4-month follow-up.

기흉을 동반한 기도이물 1예 (A Case of Bronchial Foreign Body With Contralateral Pneumothorax)

  • 나기상;김무명;김광현;박찬일
    • 대한기관식도과학회:학술대회논문집
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    • 대한기관식도과학회 1982년도 제16차 학술대회연제순서 및 초록
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    • pp.5.3-6
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    • 1982
  • 기도이물은 이비후과영역에서 드물지 않은 질환으로 이물의 種類도 다양하지만 그 개재부위도 다양하여 때로 이물제거에 수술적 방법을 요할 때도 있다. 저자들은 최근 볼펜뚜껑을 흡인한 15세의 여자환자에서 흉부X-선상좌측 폐하엽의 무기폐가 나타나고 우측에 기흉을 동반하고 있으며 기관지조영도상 좌측 하엽기관지의 완전폐새을 관찰하였다. 전신마취하에서 기관지경술에 의한 이물제거를 시도하였으나 이물이 좌측 주기관지하부에 꽉 박혀 있어 실패하였고 흉부외과에서 개흉술을 통한 기관지절개술로 이물을 제거한 1예를 체험하였기에 보고하는 바이다.

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주기관지내 전이에 의해 호흡곤란을 일으킨 직장암 1예 (A Case of Dyspnea due to Endobronchial Metastasis from Rectal Cancer)

  • 이정익;신성준;손장원;양석철;윤호주;신동호;박성수;장세진
    • 대한기관식도과학회지
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    • 제6권2호
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    • pp.204-208
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    • 2000
  • Endobronchial metastases from extrathoracic primary malignancies are uncommon. Breast, renal, and colonic carcinomas are primary sites most likely to give rise to endobronchial metastases. A number of other tumours have been reported as being complicated by endobronchial metastasis, including ovarian, thyroid, uterine, adrenal, testicular and prostatic carcinomas. The incidence of endobronchial metastasis has been estimated at 2% in patients who died of metastatic disease. Lung parenchymal metastases are common manifestations in patients with rectal cancer, however spread to the major airway is extremely rare. We herein report a case of endobronchial metastasis from rectal adenocarcinoma. A 69-year-old male patient who had been previously treated with surgical resection with rectal cancer presented with a 8-month history of gradually increasing dyspnea and non-productive cough. Clinical and radiological investigations revealed endobronchial metastasis involving, and penetrating, the lower carina and the left main bronchus. We confirmed endobronchial metastasis from the rectal carcinoma by bronchoscopic biopsy.

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Bronchial compression in an infant with isolated secundum atrial septal defect associated with severe pulmonary arterial hypertension

  • Park, Sung-Hee;Park, So-Young;Kim, Nam-Kyun;Park, Su-Jin;Park, Han-Ki;Park, Young-Hwan;Choi, Jae-Young
    • Clinical and Experimental Pediatrics
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    • 제55권8호
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    • pp.297-300
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    • 2012
  • Symptomatic pulmonary arterial hypertension (PAH) in patients with isolated atrial septal defect (ASD) is rare during infancy. We report a case of isolated ASD with severe PAH in an infant who developed airway obstruction as cardiomegaly progressed. The patient presented with recurrent severe respiratory insufficiency and failure to thrive before the repair of the ASD. Echocardiography confirmed volume overload on the right side of heart and severe PAH (tricuspid regurgitation [TR] with a peak pressure gradient of 55 to 60 mmHg). The chest radiographs demonstrated severe collapse of both lung fields, and a computed tomography scan showed narrowing of the main bronchus because of an intrinsic cause, as well as a dilated pulmonary artery compressing the main bronchus on the left and the intermediate bronchus on the right. ASD patch closure was performed when the infant was 8 months old. After the repair of the ASD, echocardiography showed improvement of PAH (TR with a peak pressure gradient of 22 to 26 mmHg), and the patient has not developed recurrent respiratory infections while showing successful catch-up growth. In infants with symptomatic isolated ASD, especially in those with respiratory insufficiency associated with severe PAH, extrinsic airway compression should be considered. Correcting any congenital heart diseases in these patients may improve their symptoms.

원발성 기관지내 평활근종 1예 (A Case of Primary Endobronchial Leiomyoma)

  • 이희경;이재형;김상헌;김태형;손장원;윤호주;신동호;박성수;민경환;백승삼;강정호
    • Tuberculosis and Respiratory Diseases
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    • 제61권3호
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    • pp.273-278
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    • 2006
  • 기관지 평활근종은 기관지에 발생하는 양성 종양으로 드문 질환이다. 기도를 폐쇄하여 호흡기계 증상을 유발할 수 있고, 원위부의 비가역적인 폐실질의 손상을 초래할 수 있으므로, 본 증례처럼 비교적 젊은 나이에서 만성 기침이나 반복되는 폐렴 등의 기관지 폐쇄의 징후가 있을 시에는, 드물지만 평활근종이 다른 기관지내의 종양과의 감별진단에 고려되어야 하고, 기관지경검사에 의한 조기 진단으로 이차적인 폐실질의 손상을 막는 것이 중요하다고 여겨진다. 이에 기관지 평활근종 1예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.