Burns Heather R, Dinis Jacob, Ding Yang, Buchanan Edward P
Michael E. DeBakey Department of Surgery, Division of Plastic Surgery, Baylor College of Medicine, Houston, Texas.
Division of Plastic Surgery, Texas Children's Hospital, Houston, Texas.
Semin Plast Surg. 2023 Nov 10;37(4):287-298. doi: 10.1055/s-0043-1775888. eCollection 2023 Nov.
Congenital ear anomalies affect 15 to 20% of neonates and can be categorized as either auricular deformations or malformations. Deformations involve a fully developed, albeit abnormally shaped, chondrocutaneous framework, which makes them amenable to correction with ear molding within the first few months of life. Malformations involve hypoplastic or fully absent auricular structures that require augmentation with alloplastic and/or autogenous reconstruction. The goal of this article is to outline the various auricular deformities and malformations, followed by a description of the latest clinical management options, both nonsurgical and surgical, by auricular anomaly.
先天性耳部异常影响15%至20%的新生儿,可分为耳廓变形或畸形。变形涉及一个发育完全但形状异常的软骨皮肤框架,这使得它们在出生后的头几个月内适合通过耳模矫正。畸形涉及发育不全或完全缺失的耳廓结构,需要通过异体和/或自体重建进行增强。本文的目的是概述各种耳廓畸形,然后描述针对耳部异常的最新非手术和手术临床管理选择。