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El tejido pulmonar anómalo, en forma de múltiples burbujas (quistes), se detecta frecuentemente antes del nacimiento mediante una ecografía prenatal periódica. Estos se denominan “quistes pulmonares congénitos”. They are also known as a congenital pulmonary airway malformation (CPAM).
Descripción
Very large lesions can be symptomatic and require drainage before birth or emergency removal immediately after delivery. However, most are asymptomatic and require no surgery in the neonatal period. Occasionally, after several months of observation, a cyst may completely disappear.
Typically, cystic malformations that persist may become infected, grow or increase the likelihood of a child developing lung tumors later in life. For these reasons, cystic malformations that don’t go away require surgery for removal.
Signos y síntomas
Fever, coughing (including coughing up blood), shortness of breath and wheezing can all be identified as signs or symptoms of lung cysts.
Tratamiento
Due to concerns for developing significant problems associated with congenital lung cysts, the definitive treatment is removing the cyst through surgery.