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相似文献

1
Schwannoma in masquerade.伪装性神经鞘瘤。
J Maxillofac Oral Surg. 2012 Sep;11(3):340-2. doi: 10.1007/s12663-011-0175-3. Epub 2011 Mar 18.
2
Neurilemmoma of Maxillary Alveolus: A Rare Case Report and Review of Literature.上颌牙槽神经鞘瘤：1例罕见病例报告及文献复习
J Pharm Bioallied Sci. 2017 Nov;9(Suppl 1):S285-S288. doi: 10.4103/jpbs.JPBS_114_17.
3
Gastric Schwannoma in an elderly man: A case report.老年男性胃神经鞘瘤 1 例报告。
Malays J Pathol. 2020 Dec;42(3):455-459.
4
Schwannoma of the descending loop of the hypoglossal nerve: case report.舌下神经降袢神经鞘瘤：病例报告
Pan Afr Med J. 2020 Jun 8;36:73. doi: 10.11604/pamj.2020.36.73.23500. eCollection 2020.
5
Brachial Plexus Schwannoma - Case Report and Literature Review.臂丛神经鞘瘤——病例报告与文献综述
Acta Clin Croat. 2018 Jun;57(2):366-371. doi: 10.20471/acc.2018.57.02.19.
6
Schwannoma in the lower lip mucosa: unexpected diagnosis.下唇黏膜神经鞘瘤：意外诊断
Quintessence Int. 2010 Oct;41(9):769-71.
7
Plexiform (multinodular) schwannoma of soft palate. Report of a case.软腭丛状（多结节性）神经鞘瘤。病例报告。
Folia Med (Plovdiv). 2012 Jul-Sep;54(3):62-4. doi: 10.2478/v10153-011-0099-1.
8
Peripheral Nerve Schwannoma: A Review of Varying Clinical Presentations and Imaging Findings.外周神经鞘瘤：不同临床表现及影像学表现综述
J Foot Ankle Surg. 2017 May-Jun;56(3):632-637. doi: 10.1053/j.jfas.2016.12.003. Epub 2017 Feb 22.
9
Giant schwannoma of the hard palate: a literature review and report of an uncommon case.硬腭巨大神经鞘瘤：文献综述及1例罕见病例报告
Gen Dent. 2018 Jan-Feb;66(1):62-65.
10
[A case of retroperitoneal schwannoma of the vagus nerve].[一例迷走神经腹膜后神经鞘瘤]
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本文引用的文献

1
Central neurilemmoma of the jaw in concurrence with radicular cyst: a case report.颌骨中央神经鞘瘤合并根端囊肿：一例报告
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Oct;102(4):e34-6. doi: 10.1016/j.tripleo.2006.01.025. Epub 2006 Aug 10.
2
A massive pleomorphic adenoma of the submandibular salivary gland accompanied by neurilemomas of the neck misdiagnosed as a malignant tumor: report of case.一例下颌下涎腺巨大多形性腺瘤伴颈部神经鞘瘤被误诊为恶性肿瘤：病例报告
J Oral Maxillofac Surg. 2001 Aug;59(8):931-5. doi: 10.1053/joms.2001.25035.
3
Schwannoma of the tongue: report of 2 cases.舌部神经鞘瘤：2例报告
J Oral Maxillofac Surg. 2001 Jul;59(7):802-4. doi: 10.1053/joms.2001.24298.
4
Schwannoma of the oral cavity. Review of the literature and report of a case.口腔神经鞘瘤。文献综述及病例报告
J Oral Med. 1984 Jan-Mar;39(1):41-3.
5
Benign solitary Schwannomas (neurilemomas).良性孤立性施万瘤（神经鞘瘤）。
Cancer. 1969 Aug;24(2):355-66. doi: 10.1002/1097-0142(196908)24:2<355::aid-cncr2820240218>3.0.co;2-2.
6
Central neurilemoma of the mandible: report of case and review of the literature.下颌骨中央神经鞘瘤：病例报告及文献复习
J Oral Surg. 1973 May;31(5):363-7.
7
Central benign and malignant neural neoplasms of the jaws: a review.
J Oral Surg. 1969 Sep;27(9):716-21.
8
Neurogenous tumors of the head and neck.头颈部神经源性肿瘤。
Cancer. 1967 Nov;20(11):1992-2001. doi: 10.1002/1097-0142(196711)20:11<1992::aid-cncr2820201127>3.0.co;2-q.
9
Neurilemmoma of the mandible. Report of a case.下颌骨神经鞘瘤。一例报告。
Br J Oral Maxillofac Surg. 1989 Dec;27(6):512-6. doi: 10.1016/s0266-4356(89)80011-7.
10
Oral manifestations of neurofibromatosis types I and II.I型和II型神经纤维瘤病的口腔表现。
Oral Surg Oral Med Oral Pathol. 1992 Mar;73(3):376-82. doi: 10.1016/0030-4220(92)90139-h.

伪装性神经鞘瘤。

Schwannoma in masquerade.

作者信息

Thomas Shaji, Vezhavendan N, Yuvaraj V, Thakur Gagan, Dal Singh V

机构信息

Department of OMFS, Peoples College of Dental Sciences, Bhopal, India ; A/160, new minal residency, J. k road, Govindpura, Bhopal, 462 023 India.

出版信息

J Maxillofac Oral Surg. 2012 Sep;11(3):340-2. doi: 10.1007/s12663-011-0175-3. Epub 2011 Mar 18.

DOI:10.1007/s12663-011-0175-3
PMID:23997489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428442/
Abstract

Neurilemmoma is a rare nerve tumor seldom included in the list of differential diagnosis of soft tissue swelling in maxillofacial region. Arrival at a clinical diagnosis of schwannomas is rarely possible as there are hardly any characteristic clinical features to help in its and it is mostly established by histopathologic examination. We report an interesting case which had presentations similar to a sebaceous cyst but finally turned out to be a schwannomma.

摘要

神经鞘瘤是一种罕见的神经肿瘤，很少被列入颌面部软组织肿胀的鉴别诊断清单。由于几乎没有任何特征性临床特征有助于做出临床诊断，神经鞘瘤很难通过临床诊断出来，大多是通过组织病理学检查确诊。我们报告了一例有趣的病例，其临床表现类似于皮脂腺囊肿，但最终确诊为神经鞘瘤。