European Journal of Plastic Surgery

, Volume 25, Issue 1, pp 29–31

Congenital midline cervical cleft: a rare embryopathogenic disorder

Authors

  •  A. Genç
    • Department of Pediatric Surgery, Faculty of Medicine, Celal Bayar University, 45020 Manisa, Turkey
  •  C. Tanelı
    • Department of Pediatric Surgery, Faculty of Medicine, Celal Bayar University, 45020 Manisa, Turkey
  •  O. Arslan
    • Department of Pediatric Surgery, Faculty of Medicine, Celal Bayar University, 45020 Manisa, Turkey
  •  Z. Dağlar
    • Department of Pediatric Surgery, Faculty of Medicine, Celal Bayar University, 45020 Manisa, Turkey
  • E Mır
    • Department of Pediatric Surgery, Faculty of Medicine, Celal Bayar University, 45020 Manisa, Turkey
Case Report

DOI: 10.1007/s00238-001-0336-6

Cite this article as:
Genç, A., Tanelı, C., Arslan, O. et al. Eur J Plast Surg (2002) 25: 29. doi:10.1007/s00238-001-0336-6

Abstract.

Congenital midline cervical cleft (CMCC) is a rare disorder of the ventral neck. The cleft consists of an epithelium-covered, longitudinal central depression with a protuberance at the cervical end. The adjacent skin is tethered by scar tissue forming a depression, which ends in a blind sinus at the caudal end. Although a variety of embryological mechanisms are proposed, its etiology is obscure. Up to the present time, fewer than 50 cases have been reported in the English literature. CMCC can be seen in association with several midline anomalies related to the branchial arches, including median cleft of the lower lip and mandible, and hypoplasia or absence of other midline neck structures. We present a 36-day-old boy with CMCC to illustrate its clinical presentation and the result at 24 months postoperatively.

Cervical cleft Midline-Neck

Copyright information

© Springer-Verlag 2002