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Sinus, fistula and cyst of branchial cleft

ICD10CM code

Name of the Condition

  • Sinus, fistula and cyst of branchial cleft

Summary

Branchial cleft anomalies, including sinuses, fistulas, and cysts, are congenital malformations that arise from incomplete obliteration of the branchial cleft structures during embryonic development. These anomalies often present as neck masses or drainage problems in children.

Causes

  • These conditions are congenital, resulting from developmental defects associated with the branchial apparatus during embryogenesis.

Risk Factors

  • An increased likelihood is present if there is a family history of branchial cleft anomalies.

Symptoms

  • Neck mass or lump
  • Recurrent neck infections
  • Discharge from small openings in the neck

Diagnosis

  • Physical examination to detect lumps or openings
  • Imaging tests such as ultrasound, MRI, or CT scan to delineate the anatomy
  • Sometimes, sinus tract exploration or fistulography may be performed

Treatment Options

  • Surgical excision is the definitive treatment to remove the sinus, fistula, or cyst and prevent recurrence or complications.

Prognosis and Follow-Up

  • Prognosis is generally excellent following complete surgical resection.
  • Regular follow-ups post-surgery may be necessary to monitor for recurrence or manage any residual symptoms.

Complications

  • Infection of the cyst or fistula
  • Potential for the cyst to enlarge or rupture
  • Cosmetic issues due to neck mass

Lifestyle & Prevention

  • There are no specific lifestyle changes or preventive measures due to the congenital nature of the condition.

When to Seek Professional Help

  • Seek medical attention if there is a noticeable lump in the neck, recurrent infections, or persistent drainage.

Additional Resources

  • American Academy of Otolaryngology–Head and Neck Surgery (AAO-HNS)
  • National Birth Defects Prevention Network

Tips for Medical Coders

  • Ensure accurate documentation of the type of branchial cleft anomaly, whether sinus, fistula, or cyst.
  • Avoid coding errors by confirming the congenital nature of the condition, as this distinguishes it from acquired conditions.

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