Congenital PS is a lesion of the lung tissue which occurs during embryonic development. The lesion is without respiratory function and shows an abnormal arterial supply. Although PS is commonly divided into two types (ILS and ELS), the clinical significance of this classification for patients with congenital PS is still controversial. In this study, we retrospectively analyzed the clinical data of 29 cases of congenital PS, including 17 cases of ILS and 12 cases of ELS. We found that ILS and ELS tend to occur in the lower lobe of the left lung. PS in other locations have also been recorded in the literature (the upper lobe, lobar isolating lung in the neck, mediastinum and abdomen), however, as this occurs rarely, they are often misdiagnosed as tumors. Therefore, for masses of unknown nature at these sites, the differential diagnosis of PS should be considered[8].
Prenatal fetal ultrasound is the standard for the diagnosis of congenital PS at present, however, compared to other imaging modalities, the ultrasound examination has higher requirements on the instrument and the operator. Chest enhanced CT can clearly display the supplying artery and abnormal vein, something that is not possible via ultrasound[9, 10]. Magnetic resonance imaging (MRI) is able to detect the relationship between lesions and abnormal supplying arteries in the systemic circulation without the use of contrast agents, however, MRI requires higher coordination in children and is not as useful as enhanced CT in revealing the features of PS[11, 12].
Currently the largest study of PS-related data, Wei et al.[13] retrospectively analyzed 2,625 cases of PS in the Chinese database, including 132 adult patients. The results of this study showed that the arterial blood supply of PS-affected lung tissues was predominantly provided by the thoracic (76.55%) and abdominal (18.47%) aortic branches. Wani et al.[14] found that the abnormal supply of systemic arteries to originate from the descending thoracic aorta (72%), the abdominal aorta, the abdominal axis or the splenic artery (21%). These results are consistent with the findings of our study, which suggest that the arterial blood supply for PS isolating lung tissue is mainly from thoracic aortic branches[15, 16].
A difference in venous drainage between ILS and ELS has also been reported in the literature, with Zhang et al.[17] finding that: in patients with ILS, the venous drainage was mainly via the pulmonary veins, and; in patients with ELS, the venous drainage was via the azygos vein or hemiazygos vein. The study also presented a difference in infection rate, with 71.17% and 31.37% for ILS and ELS, respectively. The existence of these differences between ILS and ELS in regard to symptoms, and pathological anatomy mean that it is of great clinical significance to classify PS into these two groups. However, the significance of ILS and ELS classification on surgical difficulty, treatment and prognosis of PS in children has not yet been further investigated.
In this study, a retrospective analysis of 29 children with PS was performed, resulting in the finding that the classification of these patients into ILS and ELS groups was significant for predicting their surgical outcomes. The duration of operation and postoperative hospitalization were longer in most children with ILS (p < 0.05), and intraoperative bleeding was more frequent in children with ILS (p < 0.05). More children with ILS were prone to infection, due to the lack of complete boundary between the pleura and normal lung tissue, and lack of connection to the normal trachea and bronchial tree. For the same reason, ILS lesions were also more likely to affect the surrounding normal lung tissue. The normal lung tissue after infection is brittle, more likely to bleed when touched, and more difficult to suture after bleeding. It is also more likely to cause thoracic adhesion, making intraoperative separation difficult. Due to the higher probability of lung tissue infection in children with ILS, more care should be taken, including adequate preoperative preparation, in comparison to children with ELS.
In our study, the histologic appearance of ILS and ELS showed no significant difference, with both PS types being composed of cystic dilated bronchi, bronchioles and a little immature alveolar tissue. This is consistent with the report of Richard et al. [18], who found that the histologic appearance of ELS consisted of lung tissue with acini displaying uniformly dilated bronchioles, alveolar saccules, alveolar ducts, and alveoli. As ILS and ELS appear histologically similar, the differentiation between the two is based mainly on imaging and intraoperative findings.
In summary, congenital PS is more likely to occur in the left lower lung regardless ofILS or ELS type, and most of the blood supply to the isolating lung tissue originates from the thoracic aorta. The type of congenital PS has an influence on neonates during and after operation, with ILS patients being more difficult to operate on and taking a longer time to recover. Upon histological examination, ILS and ELS showed no significant difference, thus, the differentiation between ILS and ELS needs to be made based on imaging results and intraoperative findings.