Congenital Cystic Adenomatoid Malformations Type 1: Case Report

Authors

  • Andi Dwi Bahagia Febriani Department of Pediatrics, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia; Dr. Wahidin Sudirohusodo General Hospital, Makassar, Indonesia https://orcid.org/0000-0001-6076-9995
  • Nurul Sylvana Shoraya Departement of Pediatrics, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia
  • Ema Alasiry Department of Pediatrics, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia; Dr. Wahidin Sudirohusodo General Hospital, Makassar, Indonesia

DOI:

https://doi.org/10.3889/oamjms.2022.8539

Keywords:

Congenital cystic adenomatoid malformations, Respiratory distress, Lung malformation

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.

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References

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Published

2022-02-25

How to Cite

1.
Febriani ADB, Shoraya NS, Alasiry E. Congenital Cystic Adenomatoid Malformations Type 1: Case Report. Open Access Maced J Med Sci [Internet]. 2022 Feb. 25 [cited 2024 Apr. 26];10(C):123-5. Available from: https://oamjms.eu/index.php/mjms/article/view/8539

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Case Report in Pediatrics

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