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迷走神经鞘瘤与嗜铬细胞瘤的罕见关联:一例报告

A rare association of Vagus Nerve Schwannoma and Pheochromocytoma: A case report.

作者信息

Harhar Marouane, Harouachi Abdelhakim, Bouhout Tariq, Serji Badr, El Harroudi Tijani

机构信息

Surgical Oncology Department, Regional Oncology Center, Mohammed VI University Hospital, Oujda, Morocco.

Mohammed First University Oujda, Faculty of Medicine and Pharmacy Oujda, Oujda, Morocco.

出版信息

Ann Med Surg (Lond). 2022 Mar 4;76:103475. doi: 10.1016/j.amsu.2022.103475. eCollection 2022 Apr.

DOI:10.1016/j.amsu.2022.103475
PMID:35340323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8943398/
Abstract

Vagus nerve schwannoma is a very rare benign nerve tumor. Pheochromocytoma is a rare, mostly benign tumor of the adrenal medulla with a large clinical spectrum. Their association is uncommon. The management of both tumors depends solely on surgery. The surgery of vagal schwannomas is particularly challenging considering the anatomical compositions of the area. Here, we report a case of a 76 year-old patient with cervical vagal schwannoma and benign pheochromocytoma association. We discuss the diagnosis and the surgical management of these tumors.

摘要

迷走神经鞘瘤是一种非常罕见的良性神经肿瘤。嗜铬细胞瘤是一种罕见的、大多为良性的肾上腺髓质肿瘤,临床表现多样。它们同时出现的情况并不常见。这两种肿瘤的治疗都仅依赖于手术。考虑到该区域的解剖结构,迷走神经鞘瘤的手术极具挑战性。在此,我们报告一例76岁患者,其患有颈段迷走神经鞘瘤并伴有良性嗜铬细胞瘤。我们将讨论这些肿瘤的诊断及手术治疗。

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本文引用的文献

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The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines.SCARE 2020 指南:更新共识手术病例报告(SCARE)指南。
Int J Surg. 2020 Dec;84:226-230. doi: 10.1016/j.ijsu.2020.10.034. Epub 2020 Nov 9.
2
Coughing on palpation: A rare complication of vagal schwannoma.触诊时咳嗽:迷走神经鞘瘤的一种罕见并发症。
Malays Fam Physician. 2018 Dec 31;13(3):40-43. eCollection 2018.
3
Head and Neck Schwannomas: A Surgical Challenge-A Series of 5 Cases.头颈部神经鞘瘤:一项手术挑战——5例系列报道
Case Rep Otolaryngol. 2018 Mar 4;2018:4074905. doi: 10.1155/2018/4074905. eCollection 2018.
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A Rare Case of Vagus Nerve Schwannoma Presenting as a Neck Mass.一例表现为颈部肿块的迷走神经鞘瘤罕见病例。
Am J Case Rep. 2017 Aug 21;18:908-911. doi: 10.12659/ajcr.904084.
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Pheochromocytoma: clinical review based on a rare case in adolescence.嗜铬细胞瘤:基于一例青少年罕见病例的临床综述
BMJ Case Rep. 2015 Aug 4;2015:bcr2015211184. doi: 10.1136/bcr-2015-211184.
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A literature review on surgery for cervical vagal schwannomas.关于颈段迷走神经鞘瘤手术的文献综述。
World J Surg Oncol. 2015 Mar 29;13:130. doi: 10.1186/s12957-015-0541-6.
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Extra vestibular schwannoma: a two year experience.前庭外神经鞘瘤:两年经验总结
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Cervical vagal schwannoma. A case report.颈段迷走神经鞘瘤。病例报告。
Acta Otorhinolaryngol Ital. 2009 Feb;29(1):33-5.
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Pheochromocytoma: presentation, diagnosis and treatment.嗜铬细胞瘤:临床表现、诊断与治疗
J Hypertens. 2006 Dec;24(12):2331-9. doi: 10.1097/01.hjh.0000251887.01885.54.
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[Pheochromocytoma].[嗜铬细胞瘤]
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