• 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.

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

• Tuberculosis and Respiratory Diseases
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• 제68권2호
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• pp.101-104
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• 2010

Bronchopulmonary sequestration (BPS) is a rare congenital malformation of the lower respiratory tract. Most intralobar BPSs are provided with an arterial blood via the thoracic or abdominal aorta but such a supply is rarely found in patients older than 50 years. We report a case of an intralobar BPS with a dual arterial supply from the celiac artery and thoracic aorta in a 50-year-old man presenting with a respiratory tract infection and haemoptysis. To our knowledge, this is the first case report of a BPS supplied by the celiac artery and thoracic aorta in a 50-year-old man.

• Journal of Chest Surgery
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• 제22권3호
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• pp.478-482
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• 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
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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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• 제22권2호
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• pp.308-314
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• 1989

Pulmonary sequestration is a congenital malformation characterized by an area of embryonic lung tissue that derives its blood supply from an anomalous systemic artery. Two forms recognized: extralobar and intralobar. Extralobar form is a very rare congenital malformation, usually located in the lower chest, and may be found in newborn infants at the time a congenital diaphragmatic hernia is repaired. Large sequestrated segments may be cause acute respiratory distress in the neonate. The condition is asymptomatic in 15 per cent of patients. This report presents two cases of pulmonary sequestration which misdiagnosed a superior mediastinal tumor and a benign lung tumor. First case was 30-year-old male patient and chief complaints were dyspnea, dry cough and right chest pain. Chest X-ray showed a homogenous increased density of smooth margin at the right superior mediastinal area and suggested a benign mediastinal tumor. And so explothoracotomy was made without other special studies. Second case was 28-year-old male patient. One month ago, he had tracheostomy and right closed thoracostomy due to massive hemoptysis and spontaneous hemothorax. Chest X-ray showed a benign cystic lesion at RLL area. At the time of operation, in first case, a mass of adult fist size was placed medial to the right upper lobe and densely adhesive to trachea, SVC and esophagus. Blood supply of the mass was bronchial arteries of trachea and RUL bronchus and drained to SVC and azygos vein through anomalous systemic veins. There was no bronchial communication on Frozen biopsy. In 2nd case, large cystic lesion contained old blood hematoma was located in RLL and anomalous blood vessel from thoracic aorta was drained to posterior segment of RLL. In operation field, intralobar pulmonary sequestration was diagnosed, and RLL lobectomy was carried out.

• Journal of Chest Surgery
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• 제14권4호
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• pp.350-353
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• 1981

The pulmonary sequestration is an uncommon congenital anomaly characterized by the presence of a part of lung tissue which is supplied by an aberrant artery from the aorta or its branch and usually has no communication with the normal bronchial tree. It was first presented by Hubber in 1777 and presented in details by Pryce in 1946. We present a case of extralobar pulmonary sequestration experienced recently with a case of intralobar type experienced in 1962. The patient was 11 year old male with the complaint of chronic productive cough. Serial chest films showed a large cyst with or without the air-fluid level on the posterobasal segment area of the left lower lobe. Bronchography showed no definite communication between the cyst and bronchial tree. On operation, the cystic lesion was supplied by an aberrant artery from the descending thoracic aorta 5 cm above the aortic hiatus and was sited at the posterobasal segment area of the left lower lobe. We performed the sequestrectomy and the sequestration was surrounded by its own pleura, 6.8x3.9x3.2 cm in size, contained the pale brown mucoid secretion in a large cyst and showed the primitive alveolar structure of the wall. The aberrant artery was 1 -5 cm long, 0.3 mm in internal diameter and arterio-sclerotic. We also compared 6 cases of collection, 5 intralobar and 1 extralobar type, presented in Korea.

• Journal of Chest Surgery
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• 제20권4호
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• pp.829-838
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• 1987

Bronchopulmonary sequestration is a rare congenital malformation of the lung, concerning about the abnormal feeding systemic artery, may happen a serious complication of heeding during operation if not recognized before operation. High index of suspicion of sequestration is the key to successful operative procedure with the aid of characteristic recurrent and long-standing symptoms, its location, and invasive or non-invasive diagnostic tools. We report 2 cases of intralobar type of bronchopulmonary sequestration and review 10 articles about the subject, totaling of 21 cases.

• Journal of Chest Surgery
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• 제24권3호
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• pp.292-295
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• 1991

Pulmonary sequestration is a rare congenital malformation of the lung and occasionally accompanied with upper gastrointestinal anomalies. Based on the embryologic development, they are grouped as broncho-pulmonary foregut malformation. We present one the case of the intralobar pulmonary sequestration with gastric duplication. The sequestrated pulmonary tissue was 9x7x8cm in dimension, multiseptated and multiloculated, and supplied by a systemic artery of 7mm diameter from the abdominal aorta. The gastric duplication was 8cm in diameter located at the posterior wall of the stomach without communication with the gastric lumen.

• Journal of Chest Surgery
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• 제39권7호
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• pp.556-560
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• 2006

호흡곤란을 주소로 내원한 42세 여자환자가 단순 흉부 촬영상 좌측 폐의 무기폐 소견을 보였다. 기관지 내시경과 흉부 컴퓨터 단층촬영상 좌측 주기관지에 종괴가 발견되었다. 조직검사상 종괴는 기관지 평활근종으로 진단되었다. 개흉술을 실시하여 좌측 주기관지절개를 하고 종괴를 제거하자 중엽은 정상적으로 환기가 되었다. 또한 하행대동맥에서 좌폐하엽으로 공급되는 이상동맥이 발견되어 좌폐하엽 절제수술을 동시에 실시하였다. 병리검사상 좌폐하엽은 내엽형 폐격리증으로 진단되었다. 저자들은 기관지 평활근종과 내엽형 폐격리증이 공존하는 드문 질환을 치험하였기에 보고하는 바이다.