模拟下颌唾液腺肿瘤的舌下神经鞘瘤的揭露:一例罕见的表现和外科治疗报告

Surgeries Pub Date : 2023-10-06 DOI:10.3390/surgeries4040051
Federica Maria Parisi, Antonino Maniaci, Giuseppe Broggi, Lucia Salvatorelli, Rosario Caltabiano, Roberto Lavina
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引用次数: 0

摘要

背景:神经鞘瘤是孤立的神经源性肿瘤,起源于神经鞘产生髓磷脂的细胞。舌下神经鞘瘤是非常罕见的,特别是那些起源于和模仿下颌唾液腺肿瘤的颅外肿瘤。方法:我们报告的情况下,31岁的女性谁提出了我们的耳鼻喉科的无痛性肿胀在她的左下颌下区域,持续了大约5个月。讨论:由于这些肿瘤的罕见性和独特性,全面的诊断检查是准确诊断的必要条件。手术切除仍然是金标准治疗。结论:颅外舌下神经鞘瘤是一种罕见的临床实体,需要彻底的诊断过程才能准确识别。治疗舌下神经鞘瘤的首选治疗策略是在保留面神经的同时完全切除肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unmasking Hypoglossal Nerve Schwannomas Mimicking Submandibular Salivary Gland Tumors: Case Report of a Rare Presentation and Surgical Management
Background: Schwannomas are solitary neurogenic tumors originating from the myelin-producing cells of the neural sheath. Hypoglossal nerve schwannomas are exceedingly rare, particularly those extracranially originating and mimicking a submandibular salivary gland tumor. Methods: We report the case of a 31-year-old female who presented to our ENT department with a painless swelling in her left submandibular region that has persisted for approximately five months. Discussion: Due to the rarity of these tumors and their unique nature, a comprehensive diagnostic workup is imperative for accurate diagnosis. Surgical excision remains the gold standard treatment. Conclusions: Extracranial hypoglossal nerve schwannomas represent a rare clinical entity requiring a thorough diagnostic process for precise identification. The preferred treatment strategy for managing hypoglossal gland schwannomas involves complete tumor excision while preserving the facial nerve.
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CiteScore
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