Congenital pulmonary airway malformation

Authors

  • Wlamir Pestana Ursini Hospital Guilherme Alvaro Santos, Department of Pathology Metropolitan University of Santos (UNIMES), Department of Pathology
  • Cesar Cilento Ponce Hospital Guilherme Alvaro Santos, Department of Pathology Metropolitan University of Santos (UNIMES), Department of Pathology

DOI:

https://doi.org/10.4322/acr.2018.022

Keywords:

Cystic Adenomatoid Malformation of Lung, Congenital, Respiratory Distress Syndrome, Newborn, Autopsy

Abstract

Congenital pulmonary airway malformation (CPAM) is a developmental malformation of the lower respiratory tract. We report the case of a male newborn diagnosed with cystic lung disease during prenatal ultrasound. A cesarean section was performed at the 32nd gestational week because of premature rupture of the membranes, and soon after the delivery the newborn developed respiratory failure and died. The aim of this study is to report an autopsy case because of its rarity, and to briefly discuss the CPAM subtypes and differential diagnosis of cystic lung diseases of childhood.

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Published

2018-06-13

How to Cite

Ursini, W. P., & Ponce, C. C. (2018). Congenital pulmonary airway malformation. Autopsy and Case Reports, 8(2), e2018022. https://doi.org/10.4322/acr.2018.022

Issue

Section

Article / Autopsy Case Report