• Journal of Chest Surgery
• /
• 제35권3호
• /
• pp.244-247
• /
• 2002

횡격막하 후복막강에 발생한 폐격리증은 매우 드문 선천성 기형으로 증상없이 우연히 발견되는 경우가 많으며 호발부위 위치상 다른 부신옆 종양들과 감별을 요하며 외과적 절제술로 치료된다. 저자들은 국내에서 아직 보고되지 않은 횡격막하 후복막강 폐격리증을 1례 경험하였기에 보고하는 바이다.

• Journal of Chest Surgery
• /
• 제23권2호
• /
• pp.357-361
• /
• 1990

The pulmonary sequestration is rare congenital pulmonary disease with nonfunctioning lung tissue supplied by aberrant arteries arising from systemic arteries-thoracic aorta, subclavian artery, innominate artery, internal mammary artery, etc. In our country, only 23 cases were reported previously and the majority was intralobar pulmonary sequestration except 2 cases. The patient was 17 year-old man and admitted due to intermittent cough, productive sputum and fever for 8 years. On simple chest P \ulcornerA view, multiple cysts with air-fluid levels were located at left lower lobe area. Aortogram revealed two aberrant arteries arising from thoracic aorta just above the diaphragm. On the operative field, the arteries were 0.7 and 0.3 cm in diameter. Left lower lobectomy was done with ligation of aberrant arteries. The patient was recovered and discharged uneventfully.

• Journal of Chest Surgery
• /
• 제53권2호
• /
• pp.89-91
• /
• 2020

Bronchopulmonary sequestration (BPS) is a rare congenital abnormality of the lower airway, generally characterized by blood supply received from the systemic circulation. We present a rare case of a 19-year-old man with incidentally detected BPS supplied by a branch of a pulmonary artery, rather than a systemic artery. Computed tomography showed a sequestered segment supplied by a branch of the left pulmonary artery and containing an ectopic bronchus. As chest computed tomography revealed necrosis in the sequestered tissue, infection was presumed, and the tissue was surgically removed. This may represent a very unusual occurrence, as such cases have yet to be reported in the literature.

• Journal of Chest Surgery
• /
• 제22권3호
• /
• pp.478-482
• /
• 1989

Pulmonary sequestration is applied to the congenital malformation characterized by an area of embryonic lung tissue that derives its blood supply from an anomalous systemic artery. Two cases of pulmonary sequestration were treated at the department of thoracic and cardiovascular surgery, college of medicine, Hallym University. One case was extralobar type, associated with the pneumothorax due to rupture of bulla. The other was intralobar type with symptom of massive and recurrent hemoptysis. The supplying arteries of both cases arose from the thoracic aorta. The venous return of the extralobar type was systemic into the hemiazygos vein, and that of the intralobar type was normal into the inferior pulmonary vein. Treatment for the former was resection of the sequestrated lung, and that for the latter was lobectomy of the left lower lobe. With the brief review of literature, we report the cases.

• Journal of Chest Surgery
• /
• 제27권11호
• /
• pp.930-937
• /
• 1994

Pulmonary sequestration, congenital cystic adenomatoid malformation[CCAM], infantile lobar emphysema[ILE], and bronchogenic cysts are four congenital lesions that show abnormal cystic areas within the lung field in early life. They share similar embryologic and clinical characteristics, Therefore they are sometimes difficult to make differential diagnosis each other, and all require surgical treatment. From 1984 to 1993, 20 patients underwent surgical corrections under these diagnostic categories[10 bronchogenic cyst, 4 pulmonary sequestration, 4 CCAM, and 2 ILE] in the department of thoracic & cardiovascular surgery, Inje University, Pusan Paik Hospital. There were 9 females and 11 males, Ages ranged from 26 days after birth to 69 years. Among them 5 cases of bronchogenic cyst were found out incidentally, but remained all 15 cases were noted as symptomatic cases. Recurrent pulmonary infections, respiratory distress and cough with cystic lesions in chest film were the main characteristics of them. Computed tomography and aortography were available for diagnostic conformation. For all the cases surgical resection were performed: 1 pneumonectomy, 2 bilobectomy, 9 lobectomy, 7 cyst resection and 1 mass[extralobar pulmonary sequestration] resection. All surgical treatments were well tolerated with no physical limitation. There was no operative mortality, and only one postoperative complication[empyema thoracis]. All patients were followed up ranging from 4 months to 9 years. A clinical awareness of these related lesions is important for prompt diagnosis and effective surgical treatment.

• Journal of Chest Surgery
• /
• 제30권2호
• /
• pp.226-230
• /
• 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
• /
• 제28권8호
• /
• pp.792-796
• /
• 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.

• Journal of Chest Surgery
• /
• 제4권1호
• /
• pp.55-58
• /
• 1971

Intralobar pulmonary sequestration is rare congenital lung disease, in which systemic artery supplies a congenitally cystic portion of the lung. Patient was 19 years old male whose complaints were fever, chest pain and sputum. Chest film showed a round homogenous density and air-fluid level at the left lower lung field and on bronchogram, contrast materials did not enter the abscess pocket. By operation multiple lung abscess pockets at the lower lobe were noted. An aberrant artery, measuring 0.4cm. in diameter and 2 cm. in length, arised from the aorta just above the diaphragm and entered the pusterior basal segment of left lower lobe. After division of the artery, left lower lobectomy was done ana postoperative hospital course was uneventful. Pathologic findings were multiple lung cysts which were not connected to the left lower lobe bronchi and an aberrant artery which showed elastic lamillation and mild sclerotic change.

• Journal of Chest Surgery
• /
• 제40권10호
• /
• pp.708-710
• /
• 2007

60세 여자환자가 객혈을 주소로 응급실에 내원하였다. 환자는 내원 후 시행한 흉부 컴퓨터 촬영상 가성낭종의 파열로 인한 혈흉을 동반한 내엽성 폐분리증으로 진단되었다. 수술 시 좌하엽 절제술과 기형동맥 일차 봉합술을 시행하였고, 환자는 수술 후 1주일째 합병증 없이 퇴원하였다.

• Journal of Chest Surgery
• /
• 제21권4호
• /
• pp.793-796
• /
• 1988

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 receives its blood supply from an anomalous systemic artery. We present a case of extralobar pulmonary sequestration experienced recently. The patient was 13 month old female with a complaint of fever, coughing and tachypnea. Chest film showed large homogeneous opacity in left lower lung field. At operation, a homogeneous mass was located between the left upper lobe and lower lobe, measuring 4X6X5cm in dimension. The aberrant artery was originated from the descending thoracic aorta, 1 cm in length and 3 mm in diameter. After division and ligation of the aberrant artery, sequestrectomy and lingular segmentectomy was done due to abscess formation. The postoperative course was smooth. She was discharged on postoperative thirteenth day.