One hundred and seventy-two papers were identified by searching the databases, one additional article was identified by manual searching. No reports were repetitive. Eighty-three reports were eligible for full-text screening. Of them, 38 papers matched our criteria and were included 2, 4-40. The selection study process is showed in the PRISMA flowchart in Figure 2. They included 60 cases of CBPFM. The 134 papers excluded were review articles, animal cases, published in a language other than English or malformation not meeting the diagnostic criteria depicted by Srikanth et al. Therefore, 61 cases were reviewed including our case (Table 1). The table in the appendix shows the details of the included cases.
Demographic characteristics
The gender of five cases was not reported, there were 26 males and 30 females, and male to female ratio was 0.87:1. The sex distribution among each CBPFM group was similar. The age was from 1 day to 59 years. A large proportion of these patients were aged 1 year or younger at presentation (n = 46) and 38 presented immediately after born. Seven adults have been described.
Classification and side
Among the included 61 cases, there were 13 cases in group IA, 4 cases in group IB, 18 cases in group II, 23 cases in group III and 3 cases in group IV. Forty-four malformations located in the right side, 14 in the left. Two cases had bilateral malformations. The right to left ratio was 3.1:1. The blood supply of abnormal lung tissue was reported in 39 cases, with from pulmonary artery in 17 and systematic artery in 22 respectively.
Gestation and family history
Polyhydramnios were reported in 10 cases (3 cases in Group I, 3 cases in Group II, 3 cases in Group III and 1 case in Group IV). Fetal MRI detected the tubular structure directing to the gastroesophageal junction during the second-trimester in 5 cases. These 5 cases belonged to Group III. A mass was detected in the fetal chest cavity in 2 cases. The gestation of the other cases was reported as uncomplicated or not mentioned.
There were four cases from three twins. Two cases were monochorionic, monoamniotic twins. One of them was group IA with VACTERL association, but the other one was group II without associated malformation. The other two cases were from two twins, with one of the twins affected but the siblings were normal.
Symptoms
Twenty patients presented with respiratory distress after birth. All patients with group I had drooling, feeding intolerance and failure to pass nasogastric tube because of esophageal atresia. Recurrent respiratory infection, presenting with cough and/or fever, were the main symptoms in older children and adults (10/22, 45.5%). Other symptoms included cough/choking following food intake (n=5), hemoptysis (n=2), nocturnal cough (n=1), epigastric pain (n=1).
Associated malformations
CBPFM group I was associated esophageal atresia and tracheoesophageal fistula (EA/TEF). So, EA/TEF was not counted as associated malformation in our review. Cardiovascular anomalies were the most common associated malformation (n= 11, 18.0%), followed by VACTERL association (n=6, 9.8%), skeletal malformation (n=6, 9.8%), anorectal malformation (n=2, 3.3%), diaphragmatic hernia (n=2, 3.3%) and other less frequently malformations.
Diagnosis
For group I, chest radiographs were obtained in 12 cases. The hazy hemithorax and mediastinal shift with dextrocardia were revealed in 9, hypoaerated or normal lung in 3. Only one case of CBPFM was suggested by CT scan initially. One case without chest X-ray was demonstrated during the surgery for EA/TEF. Fourteen cases with group I CBPFM were not diagnosed correctly and received operation for EA/TEF initially (ligation of tracheoesophageal fistula, primarily esophageal anastomosis or gastrostomy). Definitive diagnoses were confirmed by further evaluations that were prompted by persistent atelectasis of one lung, refractory respiratory distress or routine postoperative UGI.
Opacification of ipsilateral lung and mediastinal shift were also the uniform presentations in chest radiograph of group II (18/18). Plain X-ray in group III and group IV were reported in 11 cases. The presentations were various, including mediastinal or pulmonary mass (n=5), consolidation of part of the lung (n=6).
The diagnoses of CBPFM were confirmed by UGI in 38 case (62.3%), CT in 7 cases (11.5%), bronchoscopy in 1 case (1.6%) and intraoperative finding in 8 cases (13.1%). There were five cases diagnosed prenatally by ultrasonography and fetal MRI.
Treatment
Fifty-five cases underwent surgeries. Unilateral pneumonectomies were performed in six cases with group I, 11 cases with group II and one case with group IV. Three cases with Group IA and four cases with group II received the reimplantation of esophageal bronchus. Lobectomies or resection of aberrant lung tissue and bronchus were done in 24 cases with group IB, group III or group IV. The procedures of the other 6 cases were unknown.
Outcome
Eight patients died in this series with 4 in group I, 2 in group IB, 1 in group II and group III respectively. The mortality was 12.9%. In survivors, 27 cases were reported as doing-well or uneventful. Eight cases had respiratory morbidities such as air way stenosis, tracheomalacia, repeat respiratory infection or difficult in weaning from ventilator. Postpneumonectomy syndrome occurred in two cases. The outcomes of 15 cases were unknown.