Abstract
BACKGROUND: Congenital cystic adenomatoid malformation (CCAM) is a group of multicystic and non-cystic masses due to abnormal lung development. The incidence ranges from 1: 10,000 to 1: 35,000 pregnancies.
CASE REPORT: We report a case of a 3-day male baby presented with worsening respiratory distress, X-ray and chest CT were suggestive of CCAM, and sepsis.
CONCLUSION: The current case adds to the collective clinical and radiological knowledge of this rare congenital lung disorder.
Publisher
Scientific Foundation SPIROSKI
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