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An unusual case of anterior and posterior laryngeal cleft together: Combined cleft of larynx

机译:喉前裂和后裂共同的罕见病例:喉联合裂

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摘要

Congenital clefts of the larynx are rare and usually found dorsally. An anterior or ventral cleft of the larynx is extremely rare. Only a few patients with this defect have been reported in the literature. The purpose of this paper is to present a patient having an anterior and posterior laryngeal cleft together. A 20-year-old man presented with a history of dysphonia since childhood. He did not report symptoms of swallowing or respiration, and had no history of neck trauma. Findings of videolaryngoscopy showed a grossly abnormal larynx. The anterior commissure was wider than normal, and the vocal folds did not show a fusion anteriorly. There was an interarytenoid cleft posteriorly. A neck CT with 3D reconstruction demonstrated a ventral cleft or nonfusion of the thyroid cartilage with a posterior cricoid cleft. Barium swallow study was in normal limits. Since the patient did not have any problem with swallowing or respiration, no surgical intervention was planned, and the patient was put on speech therapy, which revealed improvement in voice. To our knowledge, this is the first case of a combined laryngeal cleft. The diagnosis is established by the clinical symptoms, endoscopic evaluation, and radiographic examinations including 3D and barium studies.
机译:先天性喉裂很少见,通常在背侧发现。喉前或腹裂极少见。文献中仅报道了少数患有这种缺陷的患者。本文的目的是介绍一个同时患有喉前裂和后裂的患者。一名20岁的男子从小就患有声史。他没有报告吞咽或呼吸道症状,也没有颈部外伤史。电视喉镜检查发现喉部严重异常。前连合处比正常人宽,并且声带未在前方融合。后面有一个腱鞘间裂。进行3D重建的颈部CT表现为腹侧裂隙或甲状腺软骨未融合,并伴有后环ic状裂。吞咽钡剂的研究处于正常范围。由于患者吞咽或呼吸没有任何问题,因此未计划进行任何手术干预,并且对患者进行了言语治疗,从而显示出声音的改善。就我们所知,这是首例合并喉裂的病例。通过临床症状,内窥镜评估和X线检查(包括3D和钡研究)来确定诊断。

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