Fourth branchial cleft anomaly in a 7-month-old infant: A case report and literature review

Kateřina Sobotková1, Milan Urík1, Klára Perce1

  • 1Department of Paediatric Otorhinolaryngology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.

Insights

Fourth branchial cleft fistula, a rare congenital neck lesion in children, can cause respiratory distress. This case highlights successful surgical and endoscopic treatment for an incomplete fistula in an infant.

Area of Science:

  • Pediatric Surgery
  • Congenital Head and Neck Anomalies
  • Otolaryngology

Background:

  • Fourth branchial cleft anomalies are uncommon congenital malformations.
  • These lesions typically manifest as inflammatory neck masses, predominantly on the left side.
  • They can present with significant complications, including airway compromise.

Purpose of the Study:

  • To report a rare case of an incomplete fourth branchial cleft fistula in an infant.
  • To describe the clinical presentation and diagnostic findings.
  • To detail the surgical and endoscopic management strategies employed.

Main Methods:

  • A 7-month-old female presented with a neck mass and respiratory distress.
  • Diagnosis of an incomplete fourth branchial cleft fistula was established.
  • Treatment involved surgical revision of a neck abscess and endoscopic plasma coblation of the pyriform fossa orifice.

Main Results:

  • The patient presented with a congenital neck mass causing respiratory distress.
  • An incomplete fourth branchial cleft fistula was diagnosed.
  • Combined surgical and endoscopic treatment successfully addressed the anomaly.

Conclusions:

  • Incomplete fourth branchial cleft fistulas are rare but critical congenital anomalies.
  • A combined surgical and endoscopic approach can be effective for managing these complex pediatric neck lesions.
  • Early diagnosis and intervention are crucial for favorable outcomes.

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