ABSTRACT

Cystic adenomatoid malformation is a rare abnormality of the lower respiratory tract, with altered development of endodermal and mesodermal structures, describes the coexistence of cystic cavities with adenomatous secretory structures, characteristic of the respiratory system. Affected patients may present respiratory distress in the perinatal, or late, period that thanks to the new imaging techniques allows us a better approach to the diagnosis and with this to a timely therapeutic resolution. We present the case of a neonate who was resolved through surgical treatment, with a successful outcome and currently with good evolution and prognosis.

KEYWORDS

Alveolar development, cystic adenomatoid malformation, prenatal diagnosis.

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