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儿童中表现为涎腺肿瘤的孤立性颌下神经鞘瘤

Solitary Submandibular Schwannoma Mimicking a Salivary Gland Tumor in a Child.

作者信息

Wong Kim Yew Richard, Hakim Ikram, Sawali Halimuddin, Lim Rachel Cui Ai, Mohd Mohsin Nur Kamilia

机构信息

Hospital Tawau, Department of Otorhinolaryngology-Head and Neck Surgery, Sabah, Malaysia.

Hospital Queen Elizabeth, Department of Otorhinolaryngology-Head and Neck Surgery, Sabah, Malaysia.

出版信息

Medeni Med J. 2024 Jun 28;39(2):132-135. doi: 10.4274/MMJ.galenos.2024.37729.

DOI:10.4274/MMJ.galenos.2024.37729
PMID:38940503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11572266/
Abstract

Tumors occurring in the submandibular space are infrequent among pediatric patients, and benign peripheral nerve tumors in this region are exceptionally rare. This study describes the uncommon occurrence of a schwannoma in the submandibular space in a child and describes its management. A 7-year-old child presented with a gradually enlarging swelling over a 7-month period in the submandibular region, clinically resembling a salivary gland tumor. There were no associated marginal mandibular, lingual, or hypoglossal nerve palsy. The mass was excised completely, and histopathological examination revealed it to be a schwannoma. It is appropriate to consider benign peripheral nerve tumors, such as schwannoma, in the differential diagnosis of submandibular space tumors in children.

摘要

儿童患者中发生于下颌下间隙的肿瘤并不常见,而该区域的良性周围神经肿瘤极为罕见。本研究描述了一名儿童下颌下间隙发生神经鞘瘤的罕见病例及其治疗情况。一名7岁儿童在7个月内下颌下区域出现逐渐增大的肿物,临床症状类似涎腺肿瘤。无相关的下颌缘支、舌神经或舌下神经麻痹。肿物被完整切除,组织病理学检查显示为神经鞘瘤。在儿童下颌下间隙肿瘤的鉴别诊断中,考虑诸如神经鞘瘤等良性周围神经肿瘤是恰当的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/094672577706/MedeniMedJ-39-132-figure-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/68bea4ae3c60/MedeniMedJ-39-132-figure-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/725ec65134fe/MedeniMedJ-39-132-figure-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/364fee564348/MedeniMedJ-39-132-figure-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/ffe776e08c70/MedeniMedJ-39-132-figure-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/094672577706/MedeniMedJ-39-132-figure-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/68bea4ae3c60/MedeniMedJ-39-132-figure-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/725ec65134fe/MedeniMedJ-39-132-figure-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/364fee564348/MedeniMedJ-39-132-figure-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/ffe776e08c70/MedeniMedJ-39-132-figure-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb6/11572266/094672577706/MedeniMedJ-39-132-figure-5.jpg

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引用本文的文献

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Submandibular schwannoma arising from the hypoglossal nerve radiologically masquerading as submandibular gland tumor.起源于舌下神经的下颌下神经鞘瘤在放射学上伪装成下颌下腺肿瘤。
J Dent Sci. 2025 Apr;20(2):1325-1327. doi: 10.1016/j.jds.2025.01.017. Epub 2025 Jan 28.
2
Letter to the Editor Regarding Our Case Report on "Solitary Submandibular Schwannoma Mimicking a Salivary Gland Tumor in a Child".致编辑的信:关于我们的病例报告“儿童中酷似涎腺肿瘤的孤立性下颌下神经鞘瘤”
Medeni Med J. 2024 Sep 30;39(3):239-240. doi: 10.4274/MMJ.galenos.2024.82710.
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Comment on "Solitary Submandibular Schwannoma Mimicking a Salivary Gland Tumor in a Child".

本文引用的文献

1
Pediatric primary salivary gland tumors.小儿原发性涎腺肿瘤
Am J Otolaryngol. 2023 Sep-Oct;44(5):103948. doi: 10.1016/j.amjoto.2023.103948. Epub 2023 Jun 8.
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A clinical study of submandibular schwannoma.下颌下神经鞘瘤的临床研究。
Oral Surg Oral Med Oral Pathol Oral Radiol. 2022 Jan;133(1):e6-e9. doi: 10.1016/j.oooo.2021.07.005. Epub 2021 Jul 16.
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Giant Solitary Schwannoma of Submandibular Salivary Gland-A Rare Entity.下颌下唾液腺巨大孤立性神经鞘瘤——一种罕见病例
关于“儿童中酷似涎腺肿瘤的孤立性颌下神经鞘瘤”的评论
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Schwannoma of the Submandibular Gland: A Rare Case Report.下颌下腺神经鞘瘤:1例罕见病例报告
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BMJ Case Rep. 2015 Aug 13;2015:bcr2015209900. doi: 10.1136/bcr-2015-209900.
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Ann Acad Med Singap. 2007 Apr;36(4):233-8.
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Ancient schwannoma of the submandibular gland: a case report.下颌下腺古老型神经鞘瘤:一例报告
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