
A 9-year-old girl with a persistent cough was diagnosed with pulmonary mucinous adenocarcinoma after a CT scan revealed a solid nodule. The tumor originated from atypical goblet cell hyperplasia, not congenital pulmonary airway malformation (CPAM). Histopathology confirmed minimally invasive adenocarcinoma with a KRAS G12D mutation. Following resection via video-assisted thoracoscopic surgery (VATS), the patient had no further complications and remained well after 11 months, highlighting the importance of identifying potential genetic mutations in rare pediatric lung cancers.
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