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Congenital Midline Cervical Cleft: A Variant of Tessier Number 30 Cleft Causing Micrognathia
Cristiano Tonello1, Ines Correia Pinto de Matos2, Leonardo Bezerra Feitosa1
1Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Brazil.
Abstract:
Congenital midline cervical cleft is a rare and generally isolated malformation of the ventral neck region with no clear etiology established. Mandibular deformities, such as micrognathia, could be considered as a consequence of a cleft cervical contracture. Complete surgical excision of the subcutaneous fibrous cord at an early age is the primary treatment modality, minimizing growth development problems on surrounding affected tissue. The aim of this study is to describe the clinical, surgical, and histological findings in a female child with congenital midline cervical cleft along with a relevant literature review. Three years follow-up after surgery exhibited satisfactory functional and cosmetic results.
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