ISSN: 2578-482X
Authors: Karavdic K , Pilav I , Mešanovic S , Spahovic R , Mesic A , Sefic Pasic I and Udovicic Gagula D
Congenital cystic adenomatoid malformation (CCAM) of the lung is a rare congenital abnormality. We present here a one month male child who had no respiratory distress after birth, but gradually developed dyspnea. The diagnosis was made prenatally. After further diagnosis (chest CT wich reveals a large lesion with mediastinal shifting ) due to the deterioration of the clinical picture, surgical treatment is indicated in the first month of life.
Keywords: Lung; Malformation; Neonatal; Early; Lobectomy
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