Pulmonary lymphangiectasia (PL) is a rare malformation characterized by dilatation of pulmonary lymphatics. This condition occurs mainly in neonatal and newborn patients. A few cases of PL occur in the young children and adult have been reported. We report another case of a 16-year-old female patient presenting with exertional dyspnea and nonproductive cough. Chest radiography shows bilateral chylous pleural effusions and perihilar interstitial infiltration. Contrast enhanced computed tomography (CT) shows bilateral pleural effusions, pericardial effusion, and lower lobes consolidation. High-resolution CT reveals interstitial changes and patchy areas of ground-glass opacity. Although no pathognomonic findings on HRCT, the interstitial process depicted this imaging tool provides the information to suggest clinical diagnosis when combined with appropriate clinical findings.