scholarly journals Thoracoscopic Lobectomy for Congenital Cystic Lung Disease in Infants

2020 ◽  
Author(s):  
Jinxi Huang ◽  
Chaoming Zhou ◽  
Qiang Chen ◽  
Dianming Wu ◽  
Junjie Hong ◽  
...  

Abstract Background: Congenital cystic lung disease is a congenital disease with abnormal development of the trachea, pulmonary parenchyma and pulmonary vessels. Congenital cystic adenomatoid malformation and pulmonary sequestration are the two main types. With the development of endoscopic technology, congenital pulmonary dysplasia has been alleviated in an increasing number of infants through thoracoscopic surgery. However, the timing of the operation is controversial.Methods: Seventy-two infants with congenital cystic lung disease who underwent thoracoscopic lobectomy from March 2017 to April 2020 were selected as subjects. The data were summarized and analysed, including preoperative complications, operative situation, postoperative recovery, postoperative hospital stay time, etc. All children were followed regularly.Results: Seventy-two patients were aged 3 to 7 months, with an average age of 5.40±2.02 months: 44 were male, and 28 were female, with an average weight of 6.95±1.96 kg. Preoperative condition: 48 patients were observed and operated on when they were between 5 and 7 months old. Twenty-four patients were diagnosed with pneumonia, and thoracoscopic surgery was performed after anti-infective therapy. All children were diagnosed with congenital cystic pulmonary disease with a CT scan before the operation. Postoperative pathological diagnosis showed 50 cases of congenital cystic adenomatoid malformation, 16 cases of intralobar pulmonary sequestration, and 6 cases of both congenital cystic adenomatoid malformation and intralobar pulmonary sequestration. Anaesthesia was performed by artificial pneumothorax or bronchial occlusion. The average operative time was 92.17±19.65 min, and the average length of postoperative ventilator assistance was 28.18±11.01 hours. Complications: 3 cases of pneumothorax after the operation and 5 cases of atelectasis, and the incidence of pneumonia was 33%. No bleeding, bronchial pleural fistula or other serious complications were observed. All children were followed for 3 months to 2 years. The growth and development of all the children were not different from those of normal children.Conclusions: In this study, preoperative pneumonia accounted for 23.6% of children. Thoracoscopic lobectomy was effective and feasible for children with congenital cystic lung disease from 3 to 7 months of age.

2004 ◽  
Vol 131A (3) ◽  
pp. 318-319 ◽  
Author(s):  
Benjamin D. Lemire ◽  
J.R. Buncic ◽  
Shelley J. Kennedy ◽  
Sarah J. Dyack ◽  
Ahmad S. Teebi

2002 ◽  
Vol 126 (8) ◽  
pp. 934-940
Author(s):  
Yukihiro Imai ◽  
Eugene J. Mark

Abstract Context.—Congenital cystic adenomatoid malformation, intralobar sequestration, extralobar sequestration, bronchopulmonary foregut malformation, bronchial atresia, and lobar emphysema generally are treated as separate entities, but there are commonalities among them. Objective.—To clarify the identity of congenital cystic adenomatoid malformation in relation to other cystic diseases. Design.—We studied 10 consecutive cases of surgically resected cystic lung disease in children. We studied the bronchial and vascular trees by mapping bronchi, pulmonary blood vessels, systemic blood vessels, the size and configuration of cysts, and associated scarring. Results.—The cystic lesions proved to be the following: 1 case of congenital cystic adenomatoid malformation, 2 cases of bronchial atresia with congenital cystic adenomatoid malformation, 1 hybrid case of congenital cystic adenomatoid malformation and intralobar sequestration, 1 case of intralobar sequestration with an aberrant hilum, 3 cases of intralobar sequestration with bronchial obliteration, 1 case of lung abscess, and 1 case of lobar emphysema. Congenital cystic adenomatoid malformation was the sole pathologic diagnosis in 1 case, but 7 other specimens had cystic adenomatoid change to various degrees. There was no bronchial connection between the cystic lesions and the patient's airway in 8 cases. The bronchial tree was absent in the cystic lung in 2 cases. Bronchus tapered into scar near the cystic lesion in 4 cases. Only 1 case had no significant bronchial abnormality. Conclusion.—The high incidence of cystic adenomatoid change in cystic lung disease associated with an abnormality of the bronchial tree suggests that cystic adenomatoid change may develop together with and be related to other congenital or acquired conditions in the lung.


2009 ◽  
Vol 44 (11) ◽  
pp. 2096-2100 ◽  
Author(s):  
Koji Komori ◽  
Shoichiro Kamagata ◽  
Seiichi Hirobe ◽  
Miki Toma ◽  
Kenji Okumura ◽  
...  

2005 ◽  
Vol 53 (1) ◽  
pp. 61-64 ◽  
Author(s):  
M. Duan ◽  
L. Wang ◽  
Y. Cao ◽  
Z. Li ◽  
W. Yang ◽  
...  

2003 ◽  
Vol 42 (3) ◽  
pp. 251-261 ◽  
Author(s):  
Elisabeth Horak ◽  
Johannes Bodner ◽  
Ingmar Gassner ◽  
Thomas Schmid ◽  
Burkhard Simma ◽  
...  

2015 ◽  
Vol 57 (2) ◽  
pp. 253-257 ◽  
Author(s):  
Ikuko Hama ◽  
Shigehiro Takahashi ◽  
Tomoo Nakamura ◽  
Yushi Ito ◽  
Kazuteru Kawasaki ◽  
...  

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