Congenital Cystic Adenomatoid Malformations Type 1: Case Report


Andi Dwi Bahagia Febriani, - and Nurul Sylvana Shoraya, - and Ema Alasiry, - Congenital Cystic Adenomatoid Malformations Type 1: Case Report. Journal of Medical Sciences. 2022.

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Abstract (Abstrak)

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.

Item Type: Article
Subjects: R Medicine > R Medicine (General)
Depositing User: - Andi Anna
Date Deposited: 27 Apr 2022 02:46
Last Modified: 27 Apr 2022 02:46
URI: http://repository.unhas.ac.id:443/id/eprint/15906

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