• 제목/요약/키워드: lung lobectomy

검색결과 429건 처리시간 0.021초

폐절제후 농흉에 합병한 견인성 중부식도게실의 치험례 (A Traction Diverticulum of the Esophagus Complicated with Empyema After Pneumonectomy)

  • 권중혁
    • Journal of Chest Surgery
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    • 제11권3호
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    • pp.359-363
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    • 1978
  • This is a case report of surgically treated esophageal traction diverticulum which was resulted from postpneumonectomy empyema. In March, 1976, left lower lobectomy and thoracoplasty were performed at a hospital to treat long standing lung abscess, after operation it developed into empyema. One year later [April, 1977], We did decortication and left upper lobectomy[ultimate pneumonectomy], which was followed by empyema again, 3 months later it developed esophagopleurocutaneous fistula. Esophagograms bowed an adult thumb tip sized traction diverticulum in the midportion of the esophagus. Finally in January, 1978, after 6 months of gastrostomy feeding, fistulectomy and diverticulectomy were performed The funnel shaped diverticulum was in midesophagus and retracted by surrounding inflammatory scar tissue. Now the postoperative course was uneventful.

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Lobectomy due to Pulmonary Vein Occlusion after Radiofrequency Ablation for Atrial Fibrillation

  • Papakonstantinou, Nikolaos A.;Zisis, Charalambos;Kouvidou, Charikleia;Stratakos, Grigoris
    • Journal of Chest Surgery
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    • 제51권4호
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    • pp.290-292
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    • 2018
  • Radiofrequency ablation is an effective treatment for atrial fibrillation. Pulmonary vein stenosis/occlusion is one of its rare complications. Herein, the case of a 50-year-old man with hemoptysis and migratory pulmonary infiltrations after transcatheter radiofrequency ablation for atrial fibrillation is presented. Initially, pneumonia, interstitial pulmonary disease, or lung cancer was suspected, but wedge resection revealed hemorrhagic infiltrations. Chest computed tomography pulmonary angiography detected no left superior pulmonary vein due to its total occlusion, and left upper lobectomy was performed. Post-ablation pulmonary vein occlusion must be strongly suspected in cases of migratory pulmonary infiltrations and/or hemoptysis.

장기역위증을 동반한 폐의 선천성낭포성 유선종기형 -치험 1례- (Congenital Cystic Adenomatoid Malformation of the Lung Associated with Situs Inversus Totalis (Report of A Case))

  • 김광호
    • Journal of Chest Surgery
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    • 제13권3호
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    • pp.292-297
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    • 1980
  • The congenital cystic adenomatoid malformation of the lung consists of an enlarged, meaty, multicystic lobe with smooth-walled cysts of varying sizes, which can communicate with major bronchi through malformed air passages that usually lacks cartilage. This abnormality is usually symptomatic in infancy with signs of respiratory distress such as tachypnea, substernal retraction and cyanosis. Prompt surgical resection is choice of treatment in life-threatening respiratory distress patients. We recently experienced a case of congenital cystic adenomatoid malformation of the lung in a patient with situs inversus totalis. The patient was 40 days old female who showed severe respiratory difficulty. Emergency left middle lobectomy was undergone successfully. Her postoperative course was uneventful. She was discharged from hospital on the postoperative eighth day in good condition.

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폐의 대세포 신경내분비암 -1례 보고- (Pulmonary Large Cell Neuroendocrine Carcinoma -One Case Report-)

  • 이석열;송철민;조현득;박형주;이철세;이길노
    • Journal of Chest Surgery
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    • 제35권12호
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    • pp.906-908
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    • 2002
  • 전신쇄약을 주소로 내원한 60세 남자환자가 흉부 방사선 사진상 좌폐하엽에서 폐종양이 발견되었다. 좌폐하엽절제술과 종격동 임파선 절제를 시행후 병리조직검사상 폐의 대세포 신경내분비암으로 진단되었다. 폐의 대세포 신경내분비암은 드문 질환으로 저자들은 이를 치험하였기에 보고하는 바이다.

전이성 폐암에 대한 외과적 요법 (Surgical Treatment of Metastatic Lung Cancer)

  • 김응중
    • Journal of Chest Surgery
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    • 제18권1호
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    • pp.86-91
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    • 1985
  • A clinical analysis was performed on 11 cases of metastatic lung cancer experienced at Department of Thoracic and Cardiovascular Surgery, Seoul National University Hospital during the 15 year period from 1970 to 1984. Of the 1lpatients of metastatic lung cancer, 4 patients were male and 7 patients were female and the age ranged from 27 years to 60 years old with the average of 38.8 years old. The sites of primary tumor were uterus and ovary in 5 patients, breast in 2, sarcoma in 2, rectum in 1 and testis in l.\ulcorner Tumor free intervals in each patients were as followed; unrecognition of primary site in 2 patients, simultaneous discovery of primary tumor and metastasis in 3, 14 months in 1, 4 years in 4 and 5 years in Twelve thoracotomies were performed in 11 patients and performed procedures were as followed; pneumonectomy in 1 patient, lobectomy in 7, wedge resection in 2, decortication and wedge resection in 1 and biopsy only in 1. Of the 11 patients, 4 patients died within one year after operation, 2 patients died within 2 years and 2 patients are alive over 5 years after operations. Other 3 patients are alive 2 months, 4 months and 9 months after operation at present.

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원발성 악성 폐 임파종 -수술 치험 1례- (Primary Malignant Lymphoma of Lung -A Case Report-)

  • 전홍주;김병훈;류지윤
    • Journal of Chest Surgery
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    • 제31권8호
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    • pp.820-822
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    • 1998
  • 원발성 악성 폐 임파종은 매우 드문 질환으로, 전체 악성 임파종의 0.34%에 불과하다. 인제 대학교 부산 백병원 흉부외과학 교실에서 경험한 증례는 76세된 남자환자로 흉부전산화 단층촬영상 임파절 종대를 동반 하지 않은 단일 종괴를 발견하고 개흉술을 통한 폐엽절제술후 병리조직학적으로 악성 임파종으로 확진되었 으며 항암화학요법을 시행하였기에 문헌 고찰과 함께 보고하고자 한다.

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폐격리증-5례 보고- (Pulmonary Sequestration: Report of 5 Cases)

  • 조대윤
    • Journal of Chest Surgery
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    • 제15권1호
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    • pp.27-34
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    • 1982
  • Pulmonary sequestration Is an unusual congenital malformation characterized by the presence of nonfunctioning lung tissue which usually has no communication with the normal bronchial tree and which receives its blood supply from an anomalous systemic artery instead of a pulmonary arterial branch. Two forms of pulmonary sequestration occur: Intralobar sequestration, in which the abnormal pulmonary tissue is incorporated within the normal lung and shares a common covering of visceral pleura, and extralobar sequestration, in which the abnormal pulmonary tissue is separated from the normal lung and has its own pleural investment. Since 1970, five cases of pulmonary sequestration were operated at the Department of Thoracic and Cardiovascular Surgery, College of Medicine, Seoul National University. 1. Among five cues, one was male and the others were female. 2. All were intralobar type and involved left lower lobe. 3. There was no operative mortality following left lower lobectomy and ligation of the aberrant artery.

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폐 평활근종;1례 보고 (Leiomyoma of the Lung - 1 Case Report -)

  • 선현;안병희;김상형;정상우
    • Journal of Chest Surgery
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    • 제25권12호
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    • pp.1444-1447
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    • 1992
  • Leiomyoma, one of the primry benign tumors of the lung, is extremely rare. Few cases reported in the literature suggest that this tumor occurs most commoly in the fourth decade and that over 90 percent of the pulmonary parenchymal leiomyomas occur in women and almost all lesions are found incidentally on chest radiographs. Treatment has been conservative surgery and 65 percent of the reported cases have been managed by lobectomy or pneumonectomy for advanced irreversible lung diseases or unw-areness of the benign nature of the lesion. This report is a case of pulmonary parenchymal leiomyoma in a 46-year-old female patient. She underwent surgical resection and the postoperative result was good.

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원발성 폐암의 외과적 고찰 (Surgical Evaluation of Bronchogenic Carcinoma)

  • 박재길
    • Journal of Chest Surgery
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    • 제27권3호
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    • pp.209-214
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    • 1994
  • Lung cancer is one of the most disastrous of all the current cancers in Korea. In 1990 it was projected that there would be 5, 500 new lung cancer patients in Korea and that 5, 000 would die of their disease. This is a mortality rate of 91 percent. We reviewed the surgically treated 153 bronchogenic cancer patients from January 1987 to December 1991 in St. Mary`s Hospital of Catholic University Medical College. There were 121 men and 32 women ranging in age from 18 to 83 years, with a mean of 56 years. Of the 153 patients, resection was possible in 138 patients and the resectability was 90.1 percent. Squamous cell carcinoma was present in 48 percent of patients, adenocarcinoma in 29 percent, adenosquamous carcinoma in 7 percent, large cell carcinoma in 6 percent, salivary gland tumor in 5 percent, and small cell carcinoma and carcinoid in 3 percent respectively. Postoperative cancer staging was grouped stage I 33 percent, stage II 21 percent, stage IIIa 35 percent, and stage IIIb 10 percent. Lobectomy was performed in 70 percent, pneumonectomy in 17 percent, and segmentectomy in 14 percent. Three and 5-year postoperative survival in resectable 138 patients were 47 and 29 percent respectively.

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폐에 발생한 점막 표피양 종양 - 1예 보고 - (Mucoepidermoid Carcinoma of the lung -A case report -)

  • 윤경찬;박이태
    • Journal of Chest Surgery
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    • 제37권1호
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    • pp.92-94
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    • 2004
  • 폐에 발생하는 점막 표피양 종양은 매우 드물며, 대부분 주로 주기관지에서 발생한다. 증상은 주로 기관 자극이나 폐쇄에 의해 발생된다. 점막 표피양 종양이 원격전이 되는 경우는 흔하지 않다. 치료는 수술적 제거가 원칙이며 예후는 종양의 조직학적 소견과 밀접한 관계가 있다. 저자의 경우 우중엽에 발생한 점막 표피양 종양을 우중엽절제술로 치험하여 양호한 결과를 보였기에 이에 보고하는 바이다.