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会厌旋转部分喉切除术及重建术治疗罕见喉神经鞘瘤:一例报告

Partial laryngectomy and reconstruction with rotation of the epiglottis in the treatment of a rare laryngeal schwannoma: a case report.

作者信息

Costa Claudiney Candido, Ramos Hugo Valter Lisboa, Alves Wilder, Lamounier Pauliana, Velasco Leandro de Castro, El Cheikh Mikhael Romanholo

机构信息

Department of Otorhinolaryngology and Head and Neck Surgery, CRER - Centro de Reabilitação e Readaptação Dr. Henrique Santillo, Goiânia, Goiás, Av. Ver. José Monteiro, 1655 - Negrão de Lima, Goiânia, 74653-230, Brazil.

出版信息

J Med Case Rep. 2020 Nov 25;14(1):229. doi: 10.1186/s13256-020-02537-z.

Abstract

BACKGROUND

Neurogenic tumors of the larynx are rare, with few cases having been reported in the literature. Schwannomas are responsible for 0.1% of all benign tumors of the larynx. They arise in the sheaths of the peripheral, autonomic, and cranial nerves. The objective of this report is to describe a case of a bulky laryngeal schwannoma, the surgical procedure for its removal, and the long-term patient follow-up.

CASE PRESENTATION

A 19-year-old Brazilian woman presented to our institution with a complaint of progressive dyspnea over the preceding year, as well as dysphonia, dysphagia for solids, and globus pharyngeus. Direct rigid laryngoscopy showed a supraglottic tumor obstructing approximately 90% of the larynx. With the symptoms progressing to severe dyspnea, an emergency tracheostomy was performed. After infusion of intravenous contrast, magnetic resonance imaging revealed a mass lesion with intense, heterogeneous contrast enhancement along the posterior wall of the hypopharynx, blocking all of the lumen and measuring 2.8 cm and 2.2 cm at its largest diameters. The image suggested a neoplastic lesion. The patient underwent open surgery for tumor resection. Her postsurgical recovery was uncomplicated. Histopathology and immunohistochemistry revealed the tumor to be a laryngeal schwannoma.

CONCLUSION

The definitive diagnosis of laryngeal lesions can be difficult, and histopathology plays a pivotal role. Laryngeal schwannomas are rare; however, tumors can become large and may ultimately lead to airway obstruction.

摘要

背景

喉神经源性肿瘤较为罕见,文献报道的病例较少。神经鞘瘤占所有喉良性肿瘤的0.1%。它们起源于周围神经、自主神经和颅神经的鞘膜。本报告的目的是描述一例巨大喉神经鞘瘤病例、其切除手术过程以及患者的长期随访情况。

病例介绍

一名19岁的巴西女性因在前一年出现进行性呼吸困难、声音嘶哑、固体食物吞咽困难和咽部异物感而前来我院就诊。直接硬喉镜检查显示声门上区肿瘤阻塞了约90%的喉部。随着症状发展为严重呼吸困难,进行了紧急气管切开术。静脉注射造影剂后,磁共振成像显示下咽后壁有一个肿块病变,有强烈的不均匀造影剂增强,阻塞了整个管腔,最大直径为2.8厘米和2.2厘米。图像提示为肿瘤性病变。患者接受了开放性肿瘤切除术。她术后恢复顺利。组织病理学和免疫组织化学检查显示肿瘤为喉神经鞘瘤。

结论

喉部病变的明确诊断可能困难,组织病理学起关键作用。喉神经鞘瘤罕见;然而,肿瘤可能会变大并最终导致气道阻塞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/7687993/64e3bfa0baca/13256_2020_2537_Fig1_HTML.jpg

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