Abstract:We report a rare case of esophageal lung in a neonate who presented with repeated chest infections and respiratory distress. Chest radiograph revealed increased opacification of the right lung with reduced lung volume and air bronchograms. Further evaluation with computed tomography (CT) showed the presence of only left mainstem bronchus at the tracheal bifurcation. Right mainstem bronchus originated from distal esophagus and aerated the right lung. Nasogastric tube was inserted into the stomach with injection… Show more
“…The clinical importance of these lesions is in those patients requiring hospitalization as they are more susceptible to recurrent pulmonary infections and respiratory failure [6] . Suspicion is usually made within the first year of life when the infant shows recurrent pulmonary infections, respiratory failure, and failure to thrive [7] .…”
“…The clinical importance of these lesions is in those patients requiring hospitalization as they are more susceptible to recurrent pulmonary infections and respiratory failure [6] . Suspicion is usually made within the first year of life when the infant shows recurrent pulmonary infections, respiratory failure, and failure to thrive [7] .…”
“…In pulmonary sequestration, there is only lobar involvement with systemic arterial supply. 5 Treatment is surgical and includes the resection of the hypoplastic lung with the repair of the esophageal communication.…”
Section: Acknowledgementmentioning
confidence: 99%
“…In agenesis, both the lung parenchyma and pulmonary artery are absent. In pulmonary sequestration, there is only lobar involvement with systemic arterial supply 5 …”
Background
Congenital bronchopulmonary foregut malformation (CBPFM) is a rare congenital malformation involving both the digestive and respiratory system. Early diagnosis is difficult, and delayed recognition may result in considerable complications. The aim of the study was to identify and analyze the clinical characteristics and radiological features of CBPFMs.
Methods
A systematic review was conducted in accordance with PRISMA guidelines. PubMed, Ovid database, EMBASE were searched for relevant publications to identify all published case-reports of CBPFM since 1992. Data about the demography, clinical presentation, pathology, imaging features, treatment and prognosis were collected.
Results
Sixty-one cases were included in our study. Cases were aged from 1 day to 59 years with the majority aged 3 years or younger. The most common type was group III (37.7%), followed by group II (29.5%)group I (27.9%) and group IV (4.9%). The presentations included respiratory distress (32.8%), cough/choking following food intake and other presentations associated respiratory infection. Thirty-eight cases (62.3%) were diagnosed by upper gastrointestinal series (UGI). Misdiagnosis was common. Eight cases (13.1%) of the included cases died.
Conclusions
Early recognition and extensive delineation of the anatomy of CBPFM are important to correct these anomalies successfully. UGI is the first choice to confirm the abnormal bronchus communicating with the esophagus. Resection of abnormal pulmonary tissue, lobe or even unilateral lung is preferred. Reconstruction procedures are feasible in selected patients.
Electronic supplementary material
The online version of this article (10.1186/s12887-019-1686-1) contains supplementary material, which is available to authorized users.
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