A rare case report of mucoepidermoid carcinoma arising in congenital cystic adenomatoid malformation
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Abstract
We report a case of 19 years old male presenting with cough and hemoptysis of 10 days duration, chest x-ray showed left hilar enlargement. Computed Tomograpy Scan-Chest showed left hilar adenopathy with segmental collapse in left upper lobe. Fibreoptic bronchoscopy revealed growth partially occluding the left main bronchus. Endobronchial biopsy showed features suggestive of squamous cell carcinoma. Left pneumonectomy with lymph node dissection done. Histopathological examination showed features of Congenital Cystic Adenomatoid Malformation (CCAM) with focus of low grade mucoepidermoid carcinoma. The literature data confirm that CCAM can rarely undergo malignant transformation and because of the risk of malignant change, early removal of CCAM of lung is advisable.
Keywords
Computed tomography Bronchoscopy PneumonectomyReferences
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