• Korean Journal of Radiology
• /
• 제22권10호
• /
• pp.1690-1696
• /
• 2021

Objective: To describe the anatomic locations and imaging features of posterior lung herniation in unilateral pulmonary agenesis and aplasia, focusing on radiograph-CT/MRI correlation. Materials and Methods: A total of 10 patients (seven with pulmonary agenesis and three with pulmonary aplasia, male: female = 1:9, mean age 7.3 years, age range from 1 month to 20 years) were included. Chest radiographs (n = 9), CT (n = 9), and MRI (n = 1) were reviewed to assess the type of lung underdevelopment, presence of anterior and posterior lung herniation, bronchus origin, supplying artery, and draining vein of the herniated lung. Results: Pulmonary agenesis/aplasia more commonly affected the left lung (n = 7) than the right lung (n = 3). Anterior lung herniation was observed in nine of the 10 patients. Posterior lung herniation was observed in seven patients with left pulmonary agenesis/aplasia. Two patients showed posterior lung herniation crossing the midline but not beyond the aorta, and five patients showed the posteriorly herniated right lower lobe crossing the midline to extend into the left hemithorax farther beyond the descending thoracic aorta through the space between the esophagus and the aorta. This anatomical configuration resulted in a characteristic radiographic finding of a radiolucent area with a convex lateral border and a vertical medial border in the left lower lung zone, revealing a tongue-like projection on CT and MRI. Conclusion: Posterior lung herniation occurs in unilateral left lung agenesis/aplasia. Approximately 70% of the cases of posterior lung herniation reveal a unique radiolucent tongue-like projection in the left lower lung zone on imaging studies, which is caused by the extension of the posteriorly herniated right lung farther beyond the descending aorta.

• Journal of Chest Surgery
• /
• 제31권6호
• /
• pp.624-628
• /
• 1998

전폐 절제술후 증후군은 드문질환이지만 종격동내 혈관의 정상적인 해부학적인 구조를 가진 대부분의 환자에서 전폐 절제술후에 지연 합병증으로 올수 있다. 이증후군의 임상증상으로는 대개 수술후 1년 이내에 나타나는 호흡곤란과 남아 있는 우측폐의 반복되는 감염이다. 전폐절제술후 이차적인 변화로 종격동이 좌측으로 끌려가면서 심장과 대혈관이 시계방향으로 회전하고 우측폐가 좌측 흉부 전방까지 확장되면서 나타나는 것으로 믿어지고 있다. 이와 같은 변화로 우측 폐동맥과 흉추사이에 끼이면서 기관과 우측 주기관지가 눌려지게 된다. 본 영동세브란스병원 흉부외과에서는 21세 여자환자에서 6년전에 기관지확장증으로 좌측 전폐절제술후 발생한 전폐절제술후 증후군을 좌측 개흉술후 종격동의 박리와 확장 보조물을 삽입하여 종격동 정복(mediastinal repositioning)을 시행하였고 환자의 증상은 수술후 소실되었으며 수술후 별다른 합병증 없이 퇴원하여 외래 추적관찰 중이다.

• Journal of Chest Surgery
• /
• 제15권4호
• /
• pp.432-439
• /
• 1982

Congenital posterolateral diaphragmatic hernia [Bochdalek hernia] is the result of a congenital diaphragmatic defect in the posterior costal part of the diaphragm in the region of the tenth and eleventh ribs. There is usually free communication between the thoracic and abdominal cavities. The defect is most commonly found on the left [90%], but may occurs on the right, where the liver often prevents detection. The male to female ratio is 2:1. Owing to the negative intrathoracic pressure, herniation of abdominal contents through the defects occurs, with resultant collapse of the lung. Shifting of mediastinum to the opposite side and compression of the opposite lung occurs. Most often these hernias are manifestated by acute respiratory distress in the newborn. A second, but less well recognized, group of patient with Bochdalek hernia survive beyond the neonatal period, usually present at a later time with "failure of thrive, intermittent vomiting, or progressive respiratory difficulty. " The diagnosis can often be made on clinical ground from the presence of respiratory distress, absence of breath sounds on the chest presence of bowel sounds over the chest . Roentgenogram of the chest confirm the diagnosis. Obstruction and strangulation have been reported but are rare. Treatment consists of early reliable identification of these congenital diaphragmatic hernia with high risk and surgical repairment. and postoperative pharmacological management with extracorporeal membranous oxygenation [=ECMO] support in the period of intensive care. On the surgical approach, for defects on left side, an abdominal incision is preferred, because of the high incidence of malrotation and obstructing duodenal bands. In the neonate, the operative mortality may be appreciable, but, later repair almost always is successful. During the period from 1972 to 1982, 4 cases of congenital Bochdalek hernia were experienced at the Kyung-Hee University Hospital.