Congenital cystic adenomatoid malformation

Below you will find more information about Congenital cystic adenomatoid malformation from Medigest. If you believe that you are suffering from any of the symptoms of Congenital cystic adenomatoid malformation it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Congenital cystic adenomatoid malformation and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Congenital cystic adenomatoid malformation comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Congenital cystic adenomatoid malformation (CAM) is categorized as a highly distinct entity, which was discovered way back in 1949. CAM is characterized as a developmental hamartomatous, an abnormality of the lung that comes with an adenomatoid abundance of cysts that resemble bronchioles.


CAM may be initially diagnosed by ultrasonography during prenatal. After birth, the chest radiography is usually performed first and CT scanning will also be necessary to assess the extent and type of the lesions.


In such special cases, a fetus that is diagnosed with CAM should be closely monitored during the pregnancy stage and perform a surgical removal after birth of the baby. For fetuses that develop some fluid collections in the chest cavity, a Harrision catheter shunt is administered to efficiently drain the accumulation of amniotic fluid. Fetus with some large cystic masses may sometimes pose serious danger during birth due to possible compression of the airways. In such cases, a surgical type of delivery is performed.


CAM is known to be a result arising from a focal arrest in the development of the fetal just before the 7th week of gestation period of the mother. However, the pulmonary development with the marked distortion may be present even at the embryonic development.

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