先天性后鼻孔闭锁:伊拉克希拉的诊断和治疗

Q4 Medicine
Saad Aljubory
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引用次数: 0

摘要

背景:后鼻孔闭锁(choana)是一种先天性疾病,患者的后鼻孔在双侧或单侧均未发育。本文旨在介绍后鼻孔闭锁的不同诊断方法:本文旨在介绍我科采用的不同诊断方法和手术治疗方法。材料和方法:本研究共纳入 21 例患者。这是一项回顾性研究。确诊的依据是 6-8-F 导管未能通过;后咽喉 CT 扫描显示闭锁板(软骨或骨)的类型和增厚情况,内窥镜检查证实了这一点。结果:女性患者 15 例,男性患者 6 例。年龄从 1 天到 25 岁不等。除一名成人患者外,所有患者都属于儿童年龄组。14名患者为单侧闭锁,7名患者为双侧闭锁。双侧耳道闭锁的患者在出生早期(1-3天)就出现了。其中五例为女性,两例为男性。单侧闭锁的病例则出现在晚期(4-25 岁)。其中男性4例,女性10例。经CT扫描证实,18名患者为骨性和膜性混合闭锁,3名患者为骨性闭锁,没有纯膜性闭锁。13 例单侧闭锁患者为右侧,只有 1 例为左侧(7.6%)。3例双侧闭锁的患者有其他先天性畸形(14%)。10例患者采用非内窥镜(经鼻)手术方法治疗(其中5例分别为双侧和单侧闭锁)。两名患者采用了内窥镜下经鼻孔手术,均为双侧耳道闭锁。九名患者采用了经鼻内窥镜方法。13名患者术后使用支架4-6周。两名患者因再次狭窄需要进行翻修手术。结论经鼻内窥镜方法是手术治疗耳道闭锁的正确方法,因为这种方法更准确,在外科医生的视野下进行,创伤更小,尽管手术时间较长,但发病率较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital atresia of posterior nares: Diagnosis and treatment at Hilla, Iraq
Background: Atresia of posterior nares (choana) is a congenital condition in which the posterior nares fail to develop either bilaterally or unilaterally. Objectives: The aim of this article is to show different methods of diagnosis and surgical procedures used for management in our department. Materials and Methods: In this study, 21 patients were included. It is a retrospective study form. The confirmation of the diagnosis is by failure of 6–8-F tube catheter to pass; CT scan of posterior choana shows the type and thickening of atretic plate (cartilage or bone), and endoscopic examination confirms it. Results: Female patients were 15, whereas male patients were 6. Age range was from 1 day to 25 years. All of the patients were within the pediatric age group except one adult patient. Unilateral cases were found in 14 patients, while 7 patients had bilateral atresia. Bilateral atresia was presented within early day life (1–3 days). They were five females and two males. The unilateral cases diagnose at a later life period (4–25 years). There were 4 males and 10 females. Proved by CT scan, mixed bony and membranous atresia were in 18 patients, bony atresia was in 3 patients, and there was no pure membranous atresia. Thirteen of the unilateral cases involved right side, while only one case had left-side atresia (7.6%). Three cases of bilateral atresia had other congenital anomalies (14%). Ten patients were treated by nonendoscopic (transnasal) surgical approach (five of them had bilateral and unilateral atresia, respectively). Endoscopic trans-septal approach was done in two patients, both had bilateral atresia. Nine patients were treated by transnasal endoscopic method. Stent was used in 13 patients postoperatively for 4–6 weeks. Two patients required revision surgery for restenosis. Conclusion: Endoscopic transnasal approach is the proper way in the surgical treatment of atresia because it is more accurate, under surgeon vision, less invasive with less morbidity in spite of longer time to perform.
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CiteScore
0.90
自引率
0.00%
发文量
21
审稿时长
8 weeks
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