Congenital Cystic Adenomatoid Malformations Type 1: Case Report | Zendy

Andi Dwi Bahagia Febriani | Zendy; Nurul Sylvana Shoraya | Zendy; Ema Alasiry | Zendy

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Congenital 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.

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