Bajaj Y, Dunaway D, Hartley B E J
Department of Otolaryngology and Plastic Surgery, Great Ormond Street Hospital, Great Ormond Street, London, UK.
J Laryngol Otol. 2004 Jul;118(7):566-9. doi: 10.1258/0022215041615074.
This is a report of a case of a rare congenital midline cervical cleft and a description of the surgical approach. Congenital midline cervical cleft is a very rare developmental anomaly. It represents a failure of the branchial arches to fuse in the midline and presents at birth with a ventral midline defect of the skin of the neck. Associated clinical features could include mandibular spurs, cleft mandible, microgenia, thyroglossal cyst, cleft lip or bronchogenic cysts. The authors present a case of a midline cervical cleft that was diagnosed and managed at an early age. They discuss the clinical presentation and embryological development of this rare condition. The operative findings, surgical excision and repair of the long vertical defect by Z-plasty are discussed in detail. The authors report a very satisfactory result following excision and Z-plasty closure of this rare congenital anomaly.
这是一例罕见的先天性颈部正中裂的病例报告及手术入路描述。先天性颈部正中裂是一种非常罕见的发育异常。它表现为鳃弓在中线处未能融合,出生时颈部皮肤出现腹侧中线缺损。相关临床特征可能包括下颌骨棘突、下颌骨裂、小下颌、甲状舌管囊肿、唇裂或支气管源性囊肿。作者报告了一例在早期被诊断和治疗的颈部正中裂病例。他们讨论了这种罕见病症的临床表现和胚胎发育。详细讨论了手术所见、通过Z成形术对长垂直缺损进行的手术切除和修复。作者报告称,切除并通过Z成形术闭合这种罕见的先天性异常后,结果非常令人满意。