Indian Journal of Pathology and Microbiology (Jan 2012)
Congenital pulmonary airway malformation with mucoepidermoid carcinoma: A case report and review of literature
Abstract
Congenital cystic adenomatoid malformations (CCAM) are rare developmental anomalies of the lung characterized by cysts of varying sizes and/or adenomatoid proliferation. Type I CCAM, the most frequent subtype, is associated with an increased incidence of malignant transformation, principally bronchioloalveolar carcinoma, with a reported incidence of around 1%. We report the first case of mucoepidermoid carcinoma arising in a type 1 CCAM.
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