Open AccessCongenital Cystic Adenomatoid Malformations Type 1: Case Report
Author(s) -
Andi Dwi Bahagia Febriani,
Nurul Sylvana Shoraya,
Ema Alasiry
Publication year - 2022
Publication title -
open access macedonian journal of medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.288
H-Index - 17
ISSN - 1857-9655
DOI - 10.3889/oamjms.2022.8539
Subject(s) - medicine , congenital cystic adenomatoid malformation , respiratory distress , radiological weapon , lung , incidence (geometry) , pediatrics , radiology , congenital malformations , pregnancy , fetus , genetics , physics , optics , biology
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.