Pulmonary sequestration
Pulmonary sequestration (pul·mo·nary - se·ques·tra·tion) is a congenital (present at birth) mass on the lungs that continues to grow to the point where it can move your organs.
What is pulmonary sequestration?
A pulmonary sequestration is a fluid-filled cyst of abnormal lung tissue that is present at birth (congenital), much like congenital pulmonary airway malformation (CPAM) .
With pulmonary sequestration, blood supply is fed into the sequestration mass directly from the aorta (the main heart artery). Due to the attached vessels and rich blood supply, the mass can grow and possibly move the heart, diaphragm (breathing muscle between the chest and abdomen) and lungs.
What are the different types of pulmonary sequestration?
There are two types of pulmonary sequestration, which are defined by the location of the mass:
Extrapulmonary (extralobular) - This type is located next to the lungs. It typically makes up about 25 percent of all cases and is often associated with other congenital conditions.
Intrapulmonary (intralobular) - This type is located inside the lungs. It typically makes up about 75 percent of all cases and is usually diagnosed later in life.
What are the signs and symptoms of pulmonary sequestration?
Physical and developmental symptoms of pulmonary sequestration include the following, which can also lead to further complications:
Accessory muscle use – heavy chest and shoulder movements, as a person struggles to breathe
Chest pains or pressure
Coughing up blood or mucus
Cyanosis – blue/gray tint to lips or fingernails
Respiratory infections – chronic (reoccurring) infections like bronchitis, colds or pneumonia
What are the causes of pulmonary sequestration?
The cause of pulmonary sequestration is unknown. Research does show that sometime during the development of the fetus in the womb, lung tissue will form abnormally, and the baby will be born with the lump or cyst.