I. G. A. Purwanthi, Agus Roy Rusly Hariantana Hamid, I Gusti Putu Hendra Sanjaya, I Made Suka Adnyana, Gede Wara Samsarga, Nyoman Siska Ananda
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引用次数: 0
摘要
背景:无其他颅面畸形的先天性舌裂是一种非常罕见的畸形。在这里,我们讨论的情况下,舌裂腭裂,报告在一个7个月大的女孩没有其他综合征或颅面异常。病例报告:本病例报告描述了一个7个月大的女孩,舌前裂,中间有一个软的、孤立的舌下肿块,大小为3厘米× 2厘米。还伴有不完全性腭裂。腭裂内可见2 cm × 2 cm大小的软孤立肿块。结果:计算机面部断层扫描(CT)显示上颌中线硬腭缺损伴完整的牙槽突。在上颌前牙槽黏膜上可见疑似脓包的带蒂囊性病变。切除舌及硬腭肿块,修复舌裂。摘要:先天性舌裂伴唇裂是一种非常罕见的畸形。早期手术干预是预防语言障碍和吞咽障碍的关键。多学科的方法,包括精心规划的分期手术和康复,对取得良好的效果至关重要。
Bifid Tongue and Cleft Palate: A Rare Congenital Malformation
Background: Congenital bifid tongue without other craniofacial abnormalities is a very rare malformation. Here, we discuss a case of the bifid tongue with cleft palate, reported in a 7-month-old girl with no other syndromes or craniofacial abnormalities.
Case Reports: This case report described a 7-month-old girl with an anterior bifid tongue, separated medially by a soft, solitary sublingual mass measuring 3 cm x 2 cm in size. There was also an associated incomplete cleft palate. A soft solitary mass measuring 2 cm x 2 cm in size was also seen within the cleft palate.
Results: Computed facial tomography (CT) revealed a midline hard palate defect with an intact alveolar process of the maxilla. Pedunculated cystic lesion suspected with epulis was noted to arise on premaxillary alveolar mucosa. Excision of the tongue and hard palate mass and repair of the bifid tongue were done.
Summary: Congenital bifid tongue with a cleft is a very rare malformation with different variations. Early surgical intervention is critical to prevent speech impairment and swallowing disorders. A multidisciplinary approach, including well-planned staged operations and rehabilitation, is important to achieve favorable outcomes.