Congenital malformations of lung
Chapter 17:Congenital malformations and chromosomal abnormalities
ICD-10 Q33 is a used to indicate a diagnosis of congenital malformations of lung.
Q33 encompasses a variety of congenital malformations of the lung, which are structural abnormalities present at birth. These malformations can include conditions such as congenital cystic adenomatoid malformation, pulmonary hypoplasia, and bronchogenic cysts, among others. The clinical significance of these conditions can vary widely, ranging from asymptomatic cases that may resolve spontaneously to severe respiratory distress requiring immediate intervention. Accurate coding is crucial for proper diagnosis, treatment planning, and tracking of these congenital anomalies in patient populations.
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Q33 includes congenital malformations such as congenital cystic adenomatoid malformation, pulmonary hypoplasia, bronchogenic cysts, and other structural lung abnormalities present at birth.
Q33 codes should be used when documenting congenital lung malformations diagnosed in newborns or infants, particularly when these conditions are identified through imaging or clinical evaluation.
Documentation for Q33 should include detailed clinical findings, imaging results, and any relevant family history of congenital conditions. Clear descriptions of the malformation and its impact on the patient's health are also necessary.
