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首页> 外文期刊>Brazilian Journal of Otorhinolaryngology >Surgical treatment of choanal atresia with transnasal endoscopic approach with stentless single side-hinged flap technique: 5 year retrospective analysis a??
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Surgical treatment of choanal atresia with transnasal endoscopic approach with stentless single side-hinged flap technique: 5 year retrospective analysis a??

机译:经鼻内镜下无支架单侧铰接皮瓣技术治疗胆道闭锁的5年回顾性分析

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Introduction: Choanal atresia is a rare congenital malformation of the nasal cavity characterized by the complete obliteration of the posterior choanae. In 67% of cases choanal atresia is unilateral, affecting mainly (71%) the right nasal cavity. In contrast to the unilateral form, bilateral choanal atresia is a life-threatening condition often associated with respiratory distress with feeding and intermittent cyanosis exacerbated by crying. Surgical treatment remains the only therapeutic option. Objective: To report our experience in the use of a transnasal endoscopic approach with stentless single side-hinged flap technique for the surgical management of choanal atresia. Methods: A 5 year retrospective analysis of surgical outcomes of 18 patients treated for choanal atresia with a transnasal technique employing a single side-hinged flap without stent placement. All subjects were assessed preoperatively with a nasal endoscopy and a Maxillofacial computed tomography scan. Results: Ten males and eight females with a mean age at the time of surgery of 20.05 ?± 11.32 years, underwent surgery for choanal atresia. Fifteen subjects (83.33%) had a bony while 3 (26.77%) a mixed bony-membranous atretic plate. Two and sixteen cases suffered from bilateral and unilateral choanal atresia respectively. No intra- and/or early postoperative complications were observed. Between 2 and 3 months after surgery two cases (11.11%) of partial restenosis were found. Only one of these presented a relapse of the nasal obstruction and was subsequently successfully repaired with a second endoscopic procedure. Conclusion: The surgical technique described follows the basic requirements of corrective surgery and allows good visualization, evaluation and treatment of the atretic plate and the posterior third of the septum, in order to create the new choanal opening. We believe that the use of a stent is not necessary, as recommended in case of other surgical techniques involving the use of more mucosal flaps.
机译:简介:胆道闭锁是一种罕见的先天性鼻腔畸形,其特征是后鼻道完全闭塞。在67%的病例中,胆道闭锁是单侧的,主要影响(71%)右鼻腔。与单侧形式相反,双侧耳道闭锁是一种危及生命的疾病,通常与呼吸窘迫有关,伴有进食和间歇性紫因哭闹而加剧。手术治疗仍然是唯一的治疗选择。目的:报告我们在使用经鼻内窥镜联合无支架单侧铰接皮瓣技术治疗胆道闭锁的经验。方法:回顾性分析了18例经鼻腔技术治疗的闭锁性闭锁患者的手术结局,该技术采用无支架置入的单侧铰链式皮瓣。术前用鼻内窥镜和颌面计算机断层扫描对所有受试者进行评估。结果:手术时平均年龄为20.05±±11.32岁的10例男性和8例女性,因进行了胆道闭锁手术。 15名受试者(83.33%)的骨质坚硬,而3名受试者(26.77%)的骨质疏松混合骨质板。分别有2例和16例患有双侧和单侧的胆道闭锁。没有观察到术中和/或术后早期并发症。术后2到3个月内,发现2例(11.11%)部分再狭窄。其中只有一个鼻塞复发,随后通过第二次内窥镜手术成功修复。结论:所描述的外科手术技术遵循矫正手术的基本要求,并可以很好地可视化,评估和治疗闭孔板和隔膜的后三分之一,以创建新的颅骨开口。我们认为,如在涉及使用更多粘膜瓣的其他外科手术技术中所建议的那样,不需要使用支架。

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