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Current Treatments for Congenital Aural Atresia
被引:0
|作者:
Lee, Min Young
[1
]
Cho, Yang-Sun
[2
]
Han, Gyu Cheol
[3
]
Oh, Jeong-Hoon
[4
]
机构:
[1] Dankook Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, Cheonan, South Korea
[2] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Seoul, South Korea
[3] Gachon Univ Med & Sci, Grad Sch Med, Dept Otolaryngol Head & Neck Surg, Incheon, South Korea
[4] Catholic Univ Korea, Coll Med, Dept Otolaryngol Head & Neck Surg, Bucheon St Marys Hosp, 327 Sosa Ro, Bucheon 14647, South Korea
来源:
关键词:
Congenital;
Ear canal;
Abnormality;
Prognosis;
SURGICAL-MANAGEMENT;
HEARING OUTCOMES;
CANAL STENOSIS;
SURGERY;
EAR;
RECONSTRUCTION;
MICROTIA;
TERM;
D O I:
10.7874/jao.2020.00325
中图分类号:
R76 [耳鼻咽喉科学];
学科分类号:
100213 ;
摘要:
Congenital aural atresia is an ear malformation evident at birth, involving various degrees of failed external ear canal development. A true external ear canal is desirable, as devices that replace the canal are inconvenient and expensive. Therefore, an optimal surgical technique is required. Here, we review useful preoperative and operative techniques. Surgical correction is often not the preferred treatment; the hearing outcome is no better than the outcomes afforded by bone-conduction devices, and surgery may be associated with recurrence or complications such as meatal stenosis. Preoperative evaluation and appropriate management are important. Several means of preventing meatal stenosis are discussed in this review.
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页码:161 / 166
页数:6
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