Prenatal diagnosis and management of fetal lung malformation

Authors

  • Wilfredo Villamonte Revista Peruana de Ginecología y Obstetricia, Lima, Perú
  • Carmen Guisse Revista Peruana de Ginecología y Obstetricia, Lima, Perú
  • Darío Escalante Revista Peruana de Ginecología y Obstetricia, Lima, Perú
  • David Acurio Revista Peruana de Ginecología y Obstetricia, Lima, Perú
  • María Jerí Revista Peruana de Ginecología y Obstetricia, Lima, Perú
  • Eliana Ojeda Revista Peruana de Ginecología y Obstetricia, Lima, Perú

DOI:

https://doi.org/10.31403/rpgo.v47i478

Abstract

The cystic adenomatous malformation (CAM) is a rare fetal lung lesion. Its frequency is about 1 in 4000 births and is characterized by an overgrowth of terminal respiratory bronchioles that form cysts of various sizes. It can be associated with polyhydramnios and pulmonary hypoplasia. We describe here a case of prenatal diagnosis and management of CAM at 3400 m (Cusco).

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Published

2015-05-10

Issue

Section

Casos Clínicos