Early Surgical Resection for Symptomatic Congenital Cystic
Adenomatoid Malformation (CCAM) in the Newborn Child

Karavdic K*, Pilav I, Mesanovic S, Spahovic R, Mesic A, Sefic Pasic I and Udovicic Gagula D

International Journal of Surgery & Surgical Techniques (IJSST)
ISSN: 2578-482X

Case Report

Early Surgical Resection for Symptomatic Congenital Cystic Adenomatoid Malformation (CCAM) in the Newborn Child

Authors: Karavdic K*, Pilav I, Mesanovic S, Spahovic R, Mesic A, Sefic Pasic I and Udovicic Gagula D

DOI: 10.23880/ijsst-16000130

Volume 2, Issue 4

Abstract

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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