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Fourth branchial cleft anomaly: management strategy in acute presentation
Filippo Carta1, Sara Sionis1, Luigi Mascia2
1Department of Otorhinolaryngology, AOU, P.O. S Giovanni di Dio, University of Cagliari, Via Ospedale 54, 09124 Cagliari, Italy.
Objectives:
Branchial malformations are common congenital head and neck lesions usually diagnosed in childhood during the first decade of life. Acute presentation is usually managed with conservative protocols before a definitive surgical procedure although the risk of life-treating septic complications may influence the physician's decision. Surgery is the treatment of choice with the removal of the lesion alone, nevertheless more aggressive approaches must be considered in complicated cases. Selective neck dissection including the removal of part of the thyroid lobe with the congenital lesion should be considered as the "ultima ratio" treatment to avoid recurrence.
Methods:
We reviewed literature and report our experience concerning two patients with fourth branchial cleft sinus.
Results:
A three-year-old child with a clinical history of recurrent neck abscess was referred to our department after several drainages performed in another centre. A three-year-old child referred to our department for a left side lower primary neck abscess. In both cases the diagnosis of a complicated fourth cleft remnant was confirmed by rigid endoscopic visualization of the mucosal orifice of the sinus in the pyriform fossa. Surgical management during acute presentation was challenging; in one patient the early fasciitis required an emergency procedure to remove the infected sinus that were strictly adherent to the deep vascular-nervous axis.
Conclusion:
Surgery was the definitive treatment in both cases and at 12 and 25 months follow-up respectively no recurrences were observed.
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