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首页|期刊导航|口腔颌面外科杂志|罕见先天性右面部不典型面横裂伴颊瘘及下颌骨角化囊肿1例报道

罕见先天性右面部不典型面横裂伴颊瘘及下颌骨角化囊肿1例报道

胡明委 宋云江 马文泽 迪力夏特·吾加西木 陈丽娟

口腔颌面外科杂志2023,Vol.33Issue(6):414-417,4.
口腔颌面外科杂志2023,Vol.33Issue(6):414-417,4.DOI:10.12439/kqhm.1005-4979.2023.06.012

罕见先天性右面部不典型面横裂伴颊瘘及下颌骨角化囊肿1例报道

Congenital atypical transverse facial cleft of the right face with buccal fistula and odontogenic keratocyst of mandible:A rare case report

胡明委 1宋云江 1马文泽 1迪力夏特·吾加西木 1陈丽娟2

作者信息

  • 1. 新疆兵团第三师图木舒克市总医院口腔科,图木舒克 843806
  • 2. 新疆兵团第三师图木舒克市总医院新生儿科,图木舒克 843806
  • 折叠

摘要

Abstract

Transverse facial cleft is a clinical type of craniofacial cleft malformation,which constitutes a rare congenital facial cleft deformity compared to cleft lip and palate.The pathogenesis of transverse facial cleft arises from incomplete fusion of maxillary process and mandibular process during embryo,resulting in a transverse facial cleft extending from the oral commissure to the buccal region.In addition to the oral and buccal malformations,developmental malformations of the first branchial arch may also co-occur,such as unilateral facial hypoplasia,preauricular fistula,appendage and other deformity.The precise pathogenesis remains unclear,potentially stemming from genetic,nutritional,or environmental factors.We present a clinical case of congenital atypical transverse facial cleft of the right face with buccal fistula and odontogenic keratocyst of mandible,thereby contributing to the clinical understanding of this condition.

关键词

第一、二鳃弓综合征/颅面裂畸形/面横裂/牙源性角化囊肿

Key words

first and second branchial arch syndrome/craniofacial cleft malformation/transverse facial cleft/odontogenic keratocyst

分类

医药卫生

引用本文复制引用

胡明委,宋云江,马文泽,迪力夏特·吾加西木,陈丽娟..罕见先天性右面部不典型面横裂伴颊瘘及下颌骨角化囊肿1例报道[J].口腔颌面外科杂志,2023,33(6):414-417,4.

口腔颌面外科杂志

OACSTPCD

1005-4979

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