Congenital malformation of breast, unspecified
ICD-10 Q83.9 is a billable code used to indicate a diagnosis of congenital malformation of breast, unspecified.
Congenital malformations of the breast can encompass a variety of conditions that affect breast development and morphology. These malformations may include hypoplasia (underdevelopment), aplasia (absence of breast tissue), or other structural anomalies. The breast tissue may be affected by genetic syndromes or environmental factors during fetal development. In pediatric patients, these conditions can lead to psychosocial issues as the child matures, particularly during puberty when breast development is expected. Diagnosis typically involves clinical examination and may be supplemented by imaging studies. The management of congenital breast malformations often requires a multidisciplinary approach, including pediatricians, surgeons, and, in some cases, geneticists, especially if associated with syndromic features. The unspecified nature of this code indicates that the specific type of malformation is not documented, which can complicate treatment planning and genetic counseling.
Detailed growth and development assessments, family history, and psychosocial evaluations.
Evaluation of breast development in a prepubescent child, referral for surgical intervention, or genetic counseling for syndromic cases.
Consideration of the psychosocial impact on the child and family, and the need for a supportive care plan.
Genetic testing results, family pedigree, and documentation of any syndromic associations.
Assessment of congenital breast malformations in the context of genetic syndromes like Turner syndrome or Poland syndrome.
Understanding the genetic basis of malformations and the implications for family members.
Used in cases of significant breast malformation requiring surgical intervention.
Preoperative assessment, surgical notes, and postoperative follow-up.
Pediatric surgical considerations for growth and development.
Document the clinical findings, any associated syndromes, family history, and psychosocial impact. Include imaging results and any referrals for surgical or genetic evaluation.
