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耳廓勺状副舟骨畸形包括变异:临床特征和一种新的手术方法。

Auricular spoon-shaped crus malformation including variants: Clinical features and a novel surgical approach.

机构信息

Seoul Center for Developmental Ear Anomalies and the BIO Plastic Surgery Group, Seoul, Republic of Korea.

出版信息

J Plast Reconstr Aesthet Surg. 2024 Sep;96:256-262. doi: 10.1016/j.bjps.2024.07.029. Epub 2024 Jul 17.

Abstract

BACKGROUND

Certain auricular malformations are uncommon and lack generally accepted diagnostic names. This study investigates an uncommon complex auricular malformation known as auricular spoon-shaped crus malformation providing a detailed description of its external characteristics. Additionally, an effective surgical approach is proposed.

METHODS

Between 1991 and 2023, 12 auricles in 11 patients with auricular spoon-shaped crus malformation including variants were surgically treated at our center. Patient medical records and photographic data were retrospectively reviewed.

RESULTS

Each auricle exhibited 2 to 4 major structural deformities within the 5 areas of the superior crus, inferior crus, and stem of the antihelix, helical crus, and earlobe. These deformities resulted in depression between the antihelix and antitragus, vertical shortening, horizontal elongation of the auricle, and/or drooping of the ear. Three patients displayed a low positioning of the malformed ear, and 8 patients exhibited mild to moderate hemifacial microsomia. In corrections we conducted earlier, we utilized various methods with variable aesthetic outcomes. Recently, an improved corrective method we implemented yielded consistently promising aesthetic results. We have confidence that adopting the surgical approach we suggest can lead to promising aesthetic results when addressing this malformation. Furthermore, we hope that the presented malformation will be recognized as a primary auricular malformation by auricular surgeons in the future.

摘要

背景

某些耳廓畸形并不常见,且缺乏普遍认可的诊断名称。本研究调查了一种罕见的复杂耳廓畸形,即耳廓匙状副舟状突畸形,详细描述了其外部特征。此外,还提出了一种有效的手术方法。

方法

1991 年至 2023 年间,我们中心对 11 例(12 只耳廓)伴有或不伴有变异的耳廓匙状副舟状突畸形患者进行了手术治疗。回顾性分析患者的病历和照片资料。

结果

每个耳廓在对耳轮上脚、对耳轮下脚和耳轮脚、对耳轮、耳舟这 5 个部位均存在 2 至 4 种主要结构畸形,导致对耳轮与对耳屏之间凹陷、垂直缩短、耳廓水平拉长和/或耳轮下垂。3 例患者的畸形耳位置较低,8 例患者存在轻度至中度的半侧颜面短小。在早期的矫正中,我们采用了多种方法,但效果各异。最近,我们采用了一种改进的矫正方法,效果一致令人满意。我们相信,采用我们建议的手术方法可以在处理这种畸形时获得良好的美学效果。此外,我们希望将来耳科医生能够将这种畸形作为一种主要的耳廓畸形来认识。

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