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经典招风耳畸形耳模塑形技术:病例报告

Classic ear moulding technique for a lop ear deformity: case report.

作者信息

Touzri Wissal, Tahiri Alaoui Mohamed El Arbi, Bentahar Oussama

机构信息

Department of Removable Prosthodontics, Faculty of Dentistry, University Mohammed V.

Faculty of Dentistry of Rabat, Avenue Allal El Fassi, Rue Mohammed Jazouli, Madinat Al Irfane, BP, Rabat Instituts, Rabat, Morocco.

出版信息

Ann Med Surg (Lond). 2024 Jul 25;86(10):6136-6139. doi: 10.1097/MS9.0000000000002379. eCollection 2024 Oct.

Abstract

INTRODUCTION AND IMPORTANCE

Lop ear is a congenital auricular deformity (CAD) detected at birth. It can negatively impact aesthetic appearance and the mental health of both the parents and the infant. Therefore, a treatment initiated at an early age is imperative.

CASE PRESENTATION

A male newborn patient on his 11th week of his life presented with his mother to the Maxillofacial Prosthodontic Unit. The extraoral examination showed a pendulous upper part of the auricle covering the antihelix with no deficiencies. The newborn's hearing function was normal and no associated syndrome was identified. The patient was diagnosed with congenital unilateral lop ear (Tanzer grade II constricted ear). A non-surgical correction with a classic ear moulding device was attempted at the 11th week after birth to reshape the abnormal ear.

CLINICAL DISCUSSION

CADs are traditionally managed by an otoplasty at age 6. Unfortunately, this option can cause many unpredictable complications, such as anaesthesia risks and under-correction. Therefore, the classic non-surgical correction of congenital auricular deformities is a non-surgical and earlier alternative to otoplasty. Moreover, many patients present at an older age; an auricular moulding device can still be a successful treatment option for these older patients.

CONCLUSION

Classic ear moulding is an early non-surgical alternative to otoplasty for managing congenital ear abnormalities. It can be initiated as early as 6 weeks after birth. Including an ear examination as a routine in every child's immediate post-birth physical examination is crucial for early diagnosis and better outcomes.

摘要

引言与重要性

垂耳是一种出生时就被发现的先天性耳部畸形(CAD)。它会对美观以及父母和婴儿的心理健康产生负面影响。因此,尽早开始治疗势在必行。

病例介绍

一名11周大的男婴随母亲前往口腔颌面修复科就诊。口外检查显示耳廓上部下垂,覆盖对耳轮,无其他缺陷。新生儿听力功能正常,未发现相关综合征。该患者被诊断为先天性单侧垂耳(坦泽II级缩耳)。出生后第11周尝试使用经典耳模装置进行非手术矫正,以重塑异常耳朵。

临床讨论

传统上,先天性耳部畸形在6岁时通过耳整形术进行治疗。不幸的是,这种选择可能会导致许多不可预测的并发症,如麻醉风险和矫正不足。因此,经典的先天性耳部畸形非手术矫正方法是一种非手术且更早的耳整形术替代方案。此外,许多患者就诊时年龄较大;耳模装置对这些年龄较大的患者仍然可能是一种成功的治疗选择。

结论

经典耳模塑形是一种用于治疗先天性耳部异常的早期非手术耳整形术替代方法。它最早可在出生后6周开始。在每个儿童出生后的即刻体检中常规进行耳部检查对于早期诊断和更好的治疗效果至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/def8/11444547/e46fe2577e6b/ms9-86-6136-g001.jpg

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