Al-Kurdi Mohammed Al-Mahdi, Razzouk Qusai, Hussein Othman Sheikh, Sawas Raghad, Morjan Mohamad
Faculty of Medicine, University of Aleppo, Aleppo, Syrian Arab Republic.
Faculty of Medicine, University of Aleppo, Aleppo, Syrian Arab Republic.
Int J Surg Case Rep. 2023 Sep;110:108626. doi: 10.1016/j.ijscr.2023.108626. Epub 2023 Aug 11.
Congenital laryngeal cysts are a rare cause of stridor in infants, and vallecular cysts account for 10.5-20.1% of all congenital laryngeal cysts. Large cysts can lead to airway obstruction and death. Nasopharyngolaryngoscopy is needed to confirm the diagnosis. Surgical treatment relieves symptoms and prevent serious complications. We report a congenital laryngeal cyst on the lingual surface of the epiglottis in a female newborn that was successfully excised without any complications.
A 15-day-old female newborn presented with stridor, dysphagia and dyspnea that worsened and eventually led to a diagnosis of a large serous cyst on the epiglottis's lingual surface, compressing the entrance to the larynx. Surgery was performed under general anesthesia and the entire cyst was excised using rigid endoscopy. After the surgery, the infant made a quick recovery with no complications or recurrence.
Vallecular cysts are a rare type of laryngeal cysts and an uncommon cause of congenital stridor that requires immediate diagnosis and management to prevent upper airway obstruction and death. Clinical features vary depending on the patient's and cyst's characteristics. Laryngoscope can help in confirming the final diagnosis. Complete excision is a better than aspiration, as it has a lower recurrence rate.
Vallecular cysts are a life-threatening condition that requires early diagnosis and immediate management to avoid any potential complications. It must be taken into account in the presence of congenital stridor. Marsupialization and excision (extirpation) have equal effectiveness and low recurrence rate, making them definitive surgical treatments for vallecular cysts.
先天性喉囊肿是婴儿喘鸣的罕见原因,会厌囊肿占所有先天性喉囊肿的10.5 - 20.1%。大囊肿可导致气道阻塞和死亡。需要进行鼻咽喉镜检查以确诊。手术治疗可缓解症状并预防严重并发症。我们报告一例女性新生儿会厌舌面的先天性喉囊肿,成功切除且无任何并发症。
一名15日龄女性新生儿出现喘鸣、吞咽困难和呼吸困难,症状加重,最终诊断为会厌舌面的一个大浆液性囊肿,压迫喉入口。在全身麻醉下进行手术,使用硬性内镜切除整个囊肿。术后,婴儿恢复迅速,无并发症或复发。
会厌囊肿是一种罕见的喉囊肿类型,是先天性喘鸣的不常见原因,需要立即诊断和处理以预防上气道阻塞和死亡。临床特征因患者和囊肿的特点而异。喉镜有助于确诊。完整切除优于抽吸,因为其复发率较低。
会厌囊肿是一种危及生命的疾病,需要早期诊断和立即处理以避免任何潜在并发症。在存在先天性喘鸣的情况下必须予以考虑。袋形缝合术和切除术(摘除术)具有相同的疗效和低复发率,使其成为会厌囊肿的确定性手术治疗方法。