先天性声带畸形1例:手术及4年随访

Parit Ladani, Niyati Balse, B. Jayakar, H. Sailer
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引用次数: 0

摘要

合颚畸形是一种极为罕见的颅面畸形,在较小或较大程度上影响上下颌,尤其是邻近的骨和软组织。颌骨融合会导致并发症,如气道和呼吸受损、进食困难和生长不良。早期的多学科干预、在适当的时间进行手术和细致的术后监测是其管理的当务之急。我们描述了一个6个月大的儿童先天性同颌畸形的病例,该病例得到了成功的治疗。四年的随访显示,结果令人满意,生长完成后需要进行颌骨矫正手术,以改善功能和美观。详细讨论了麻醉注意事项、喂养、手术管理、术后护理、随访以及生长调节。
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Case report on congenital syngnathia: Surgery and a 4-year follow-up
Syngnathia is an extremely rare craniofacial malformation affecting the upper and lower jaws, in particular, and adjacent bony and soft tissues, to lesser or greater extent. Fusion of jaws leads to complications such as compromised airway and breathing, feeding difficulty, and poor growth. An early multidisciplinary intervention, surgery at the appropriate time, and meticulous postoperative monitoring are most imperative in its management. We describe a case of a 6-month-old child with congenital syngnathia that was managed successfully. Four-year follow-up revealed satisfactory outcomes and the need for corrective jaw surgeries after growth completion for improved function and esthetics. Anesthesia considerations, feeding, surgical management, postoperative care, and follow-up as well as growth regulation have been discussed in detail.
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审稿时长
16 weeks
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