Section: Head and neck Curriculum: Curriculum, page 43

Definition

  • Failure of obliteration of branchial clefts 1-4

Epidemiology


Aetiology


  • Remnant of branchial cleft

  • Incomplete involution of the pharyngeal cleft


Pathophysiology 


  • Lead to:

    • Cyst, fistula, sinus

  • Can become infected


Clinical


  • Lateral swelling in the neck, anterior to SCM

  • Swallowing or airway difficulties

  • +/- fistula or sinus

  • Will not move on swallowing

  • Pharyngeal oedema - airway and swallowing difficulties

  • Locations
    • 1st
      • Smooth, tender, non-fluctuant mass between ear canal and submandibular area
      • Cutaneous punctum that fluid can be expressed through
      • Can involve parotid, facial N and ear canal
    • 2nd
      • Punctum lower ant border SCM
      • Connect to tonsil fossa
      • Related to carotids (between) and CN 9/12 - superficial
      • Can cause AW compromise
    • 3rd/4th
      • Left neck, suprasternal notch/clavicular area
      • Firm masses are more likely recurrent infection related

Locations

1st - angle of mandible or within submandibular region 2nd - ant/med to SCM 3rd - middle/lower ⅓ ant SCM (punctum) 4th - middle/lower ⅓ ant SCM (punctum)

Classification 


  • Based on their internal opening due to their Pharyngeal cleft of origin


  • Classified 


    • First - External Auditory canal 

      • Course high 

      • With fistula through the parotid / Periauricular

      • Lateral to facial nerve 

    • Second - Tonsillar fossa

      • Exist along the anterior boarder of SCM 

      • Fistula through the platysma and ascent along carotid sheath

      • Passing between Internal Carotid and External Carotid Arteries

      • Caution CN IX, X, XI

      • Most common

    • Third - Pyriform Sinus

      • Lower in neck Anterior to SCM

      • Posterior to the Internal Carotid Artery

    • Fourth - Apex of Pyriform Sinus

      • Rare and do not fistulate

  • Recurrent infections 


    • Can cause Fistulas


Investigations

  • USS - confirm cystic nature
  • OGD/flexible nasendoscopy if suspect fistula
  • CT - localise tract and plan surgery
  • Sinogram - to visualise tract

Management


Summary

  • Congenital epithelial cysts
    • Develop due to INCOMPLETE INVOLUTION OF BRANCHIAL CLEFT STRUCTURES
  • 4 types correlating to 4 clefts
    • Cleft 2 is the most common
  • Minimal malignancy risk
  • Can cause cyst formation, sinus and fistula with recurrent infection
  • Cleft 2 cyst has a punctum at the skin ant to SCM midpoint
  • Track heads deep to platysma, between carotid bifurcation and superficial to CN 9 and 12 to reach the tonsillar fossa
  • Dx is clinical with further characterization by cross sectional imaging and sinograph
  • Mx includes abx for infection and definite surgical fistula tract ligation and division