Congenital malformations of spleen
ICD-10 Q89.09 is a billable code used to indicate a diagnosis of congenital malformations of spleen.
Congenital malformations of the spleen encompass a variety of structural anomalies that can affect the organ's size, shape, and function. These malformations may include asplenia (absence of the spleen), polysplenia (multiple small spleens), and ectopic spleen (spleen located in an abnormal position). Such conditions can lead to significant clinical implications, including increased susceptibility to infections due to impaired immune function, particularly in cases of asplenia. Diagnosis typically involves imaging studies such as ultrasound or MRI, and management may require surgical intervention or close monitoring. The presence of these malformations can also be associated with other congenital syndromes, necessitating a comprehensive evaluation of the patient’s overall health and any additional congenital anomalies. Accurate coding is crucial for proper management and follow-up care, as well as for understanding the potential complications associated with these conditions.
Pediatric documentation should include growth parameters, developmental milestones, and any associated congenital anomalies.
Common scenarios include newborns presenting with splenic anomalies during routine examinations or imaging for other conditions.
Consideration of the child's overall health and any syndromic associations is crucial for accurate coding.
Genetic documentation should include family history, genetic testing results, and any syndromic associations.
Scenarios may involve genetic counseling for families with a history of congenital malformations or syndromes.
Understanding the genetic basis of congenital malformations is essential for accurate coding and management.
Used to evaluate congenital malformations of the spleen in pediatric patients.
Documentation must include indications for the ultrasound and findings related to splenic anomalies.
Pediatric specialists should ensure that imaging findings correlate with clinical symptoms.
Common congenital malformations of the spleen include asplenia, polysplenia, and ectopic spleen. These conditions can lead to various clinical implications, including increased risk of infections and may require surgical intervention or monitoring.
