Case Report Congenital lobar emphysema in an adult

in the adult can be a challenge, as the abnormality may be mistaken for something more sinister. Congenital lobar emphysema (CLE) is a lung bud (bronchopulmonary) anomaly, usually detected in the neonatal period and early childhood.CLE is almost always unilateral with a male preponderance (M: F=3:1). This disease is characterized by hyperinflation of one or more lobes of the lung, leading to compression atelectasis on the ipsilateral or contralateral side and mediastinal shift. These, in turn, produce ventilation-perfusion mismatch. [1] We report this rare case from a northern state of India with the peculiarity of being found in an adult who is on conservative treatment. ABSTRACT Congenital lobar emphysema (CLE) is a clinico-radiological diagnosis, seen usually by four-six weeks of age (50% of patients) and rarely (<5% of patients) after the age of six months. Here, we report a young male with gradual onset of mild exertional breathlessness and physical examination revealing the features of right sided pneumothorax. X-ray of chest, with subsequent CT of chest, leads to the diagnosis of CLE. The pulmonary function tests, bronchoscopic examination and α 1 -antitrypsin level are normal. Patient is managed conservatively.


INTRODUCTION
Developmental lung anomalies in the adult can be a challenge, as the abnormality may be mistaken for something more sinister. Congenital lobar emphysema (CLE) is a lung bud (bronchopulmonary) anomaly, usually detected in the neonatal period and early childhood.CLE is almost always unilateral with a male preponderance (M: F=3:1). This disease is characterized by hyperinflation of one or more lobes of the lung, leading to compression atelectasis on the ipsilateral or contralateral side and mediastinal shift. These, in turn, produce ventilationperfusion mismatch. [1] We report this rare case from a northern state of India with the peculiarity of being found in an adult who is on conservative treatment.

CASE REPORT
A 19-years-old male presented to our hospital with mild breathlessness on exertion from two months, denying any history of fever, hemoptysis or cough. On general physical examination, pulse of 82 beats per minute, blood pressure of 120/70 mmHg and respiratory rate of 16 per minute α 1 -antitrypsin level was 121 mg/dl. Then the patient was subjected to bronchoscopic examination to find any intraluminal etiology, but revealed no abnormality. Lastly, echocardiography was done to find any cardiac lesion that was normal.
Congenital lobar emphysema (CLE) was the only possibility in this patient because clinical and radiological features were absolute for this rare diagnosis. Patient is in our close follow up and is on conservative treatment because the symptoms were mild and he declined surgical option. Till last follow-up visit, patient was stable with no clinical progression of the disease based on frequent clinical assessments with serial X-rays of chest, pulmonary function tests and arterial blood gas analysis.

DISCUSSION
CLE is characterized by variable severe overinflation of a pulmonary lobe, and compression of surrounding lung parenchyma. Pulmonary vascular markings can be seen up to the periphery of the affected lobe and there is no pleural demarcation as we see in pneumothorax. Mostly single lobe on one side is involved; however, multilobar involvement can be seen. Pulmonary lobes commonly involved are left upperlobe (43%), right middle lobe (32%), and right upper lobe (20%). [1] Adult presentation is unusual. They usually come with exertional dyspnoea or pulmonary infections. Symptoms can be mild and sometimes no symptoms can be seen.
The etiology of CLE is difficult to determine and no apparent cause is found in 50% of cases. Most commonly, the cause is a congenital defect of cartilage, ranging from hypoplastic and flaccid tissue to complete absence, accounting for 25% of cases. The remaining 25% have other causes of bronchial obstruction, such as redundant mucosal fold, mucus plugging, anomalous cardiopulmonary architectures and rarely intrathoracic masses. [2] There are now data from molecular, genetic and embryonic organ culture studies that indicate that normal primary branching pattern of lung development is regulated by reiterative signaling of a fibroblast growth factor-10 pathway. Secondary branching appears to be dependent on the influence of sonic hedgehog and one of the Homeobox genes, Nkx 2.1, also identified as thyroid transcription factor-1. Although significant mutations in the genetic material controlling these functions appear to result in major anomalies, minor errors in transcription might result in localized deficiencies in the bronchial cartilage leading to the development of CLE. The reiterative nature  of signaling also might help in explaining cases in which multiple lobes are affected. [3] Association between congenital heart disease and CLE has been described. Murray et al. showed a 14% incidence of congenital heart diseases among 166 CLE patients. Common cardiac defects were left to right shunt, tetrology of fallot, right sided aortic arch and patent ductus arteriosus. [4,5] Pulmonary function tests in CLE can be normal in asymptomatic or mild disease, but obstructive pattern is a feature of moderate to severe disease. Radiologically, the cardinal features are overinflation and air trapping, the former is manifested by markedly increased volume of the affected lobe, depressing the ipsilateral diaphragm, compressing the surrounding lung parenchyma and displacing the mediastinum. Vascular markings in the affected lobe are attenuated but maintained till the periphery of the lung. There is no line of pleural demarcation in contrast to pneumothorax. Chest X-ray and CT scan usually establish the diagnosis. Other imaging modalities include MRI and V/Q scan. MRI demonstrates any vascular lesion causing external compression but it is only an adjunct to the diagnosis of CLE, not a primary investigation. V/Q scan depicts ventilation defects and decreased perfusion in the hyoperexpanded lobe due to attenuated vascularity. [6] Pulmonary lobectomy of involved lobe is the treatment of choice for CLE. [7] PS Critchley and colleagues [8] reported a young pregnant female with left upper lobe CLE and managed by the resection of the involved lobe. [8] Granato F [9] reported first case of endoscopic parenchymal sparing resection in CLE with mild symptoms. Thus video assisted thoracoscopic surgery (VATS) seems to be an emerging and advantageous approach. Dutta et al. [10] from India reported conservative treatment of a neonate with CLE and Meir Mei-Zahav et al. [11] managed 14 children (0-17 years) conservatively out of 20 children with CLE. However, studies are further required to determine the long-term outcome of conservative management, as the disease is rare in adults. Going through the literature, surgical option is the suitable one and VATS can be promising in future.