1.
Ginecol. & obstet
; 47(1): 65-68, ene. 2001.
Artigo
em Espanhol
| LIPECS
| ID: biblio-1108563
RESUMO
La malformación adenomatosa quística (MAQ) es una rara lesión pulmonar fetal y se caracteriza por un crecimiento exagerado de los bronquiolos terminales, los cuales forman quistes. Describimos un caso de diagnóstico y manejo prenatal y postnatal de MAQ a 3,400 msnm (Cusco).
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).