病例报告：儿童咽喉闭锁

Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya Pub Date : 2024-04-20 DOI:10.32539/jkk.v11i2.420

Christopher Martinus Susanto, Guntur Surya

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引用次数: 0

摘要

蝶窦闭锁是一种先天性疾病，是由于蝶窦膜从胚胎时期就未能分裂，导致一侧或双侧蝶窦出现膜或骨。目前，关于各种手术技术的有效性以及术后使用支架和抗肿瘤药物的必要性仍存在争议。提供有关噎管闭锁的诊断和治疗信息。一名患有双侧噎管闭锁的 15 岁女性。患者接受了鼻内噎管成形术。直到术后第 8 周进行评估时，噎管才获得专利。噎管闭锁的处理。用粘膜网片制作新单孔是治疗噎管闭锁的有效手术方法之一。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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CASE REPORT: CHOANAL ATRESIA IN CHILDREN

Choanal atresia is a disorder in which there is a congenital membrane or bone in one or both choanas due to the failure of the buconasalis membrane to divide from the embryonic period. Currently, there is still controversy about the effectiveness of various surgical techniques and the need for post-surgical use of stents and anti-neoplastic agents. Provides information regarding the diagnosis and management of choanal atresia. A 15-year-old female with bilateral choanal atresia. The patient underwent endonasal choanoplasty. Choanal was patented until the 8th week of post-operative evaluation. Management of choanal atresia. Making a neo-unicoana with a mucosal mesh is one of the effective surgical techniques for treating choanal atresia

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Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya

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