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先天性多发性唇系带在临床上比较罕见,我科遇1例多发性唇系带合并唇瘘患者,报告如下: 患者,卜××,女,23岁,工人。病史:该患者为早产第4胎,生后即发现上、下唇有多条粘膜束带。为修复上颌牙间隙,要求手术矫治上唇粘膜束带,于1986年12月12日来我科就诊。家族中无类似病例。口腔颌面部所见:面部对称,鼻尖上翘,酷似“朝天鼻”。32 23牙间隙各宽0.6cm,在其牙间隙中间牙槽脊至上唇唇红粘膜各有-2.0cm长,中份宽1.0cm扇形粘膜束带,上唇系带位置正常,在其右侧
Congenital multiple lip lace in the clinical relatively rare, I encountered a case of multiple lip lace patients with lip fistula, the report is as follows: Patients, BU × ×, female, 23 years old, workers. History: The patient is the fourth child of prematurity, after birth that found on the lower lip mucosal band. In order to repair maxillary teeth gap, requiring surgical correction of the upper lip mucosal band, December 12, 1986 to our department. No similar cases in the family. Oral and maxillofacial see: facial symmetry, nose upturned, resembles “astronomical nose.” 32 23 teeth wide and 0.6cm wide, in the middle of its teeth between the alveolar ridge to the upper lip red mucosa -2.0cm long, 1.0cm wide fan in the mucosal band, the upper lip lace normal position on the right