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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Congenital pulmonary airway malformation &#40;CPAM&#41; is a rare entity with potential for malignant transformation&#46; We describe the case of a fourteen-year-old boy evaluated for the presence of a nodular image on the right lung on the chest x-ray&#46; Computerized Tomography &#40;CT&#41; showed a round lesion of medium density with cavitation on the right lung&#46; After one year of follow-up the patient was still asymptomatic and the image was similar&#46; With the agreement of the cardiothoracic surgeons an excisional biopsy was performed&#46; The histological examination revealed a mucinous bronchioloalveolar carcinoma associated with a type 1 CPAM&#46; The patient was then submitted to right inferior lobectomy&#46; After two years follow-up he is asymptomatic and free of complications&#46; To the authors best knowledge this is the first case reported in Portugal of this rare association&#46; The approach to cystic lesions in asymptomatic patients is discussed&#46;</p>"
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