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本文引用的文献

1
National Comprehensive Cancer Network Guideline Recommendations of Cancer Drugs With Accelerated Approval.国家综合癌症网络指南推荐加速批准的癌症药物。
JAMA Netw Open. 2023 Nov 1;6(11):e2343285. doi: 10.1001/jamanetworkopen.2023.43285.
2
Malignant peripheral nerve sheath tumors of the sino-nasal tract: about an unusual case report.鼻窦恶性周围神经鞘瘤:一例罕见病例报告
J Surg Case Rep. 2022 Feb 18;2022(2):rjac028. doi: 10.1093/jscr/rjac028. eCollection 2022 Feb.
3
Malignant Peripheral Nerve Sheath Tumor in the Nasal Cavity of a Neonate: A Case Report.新生儿鼻腔内的恶性外周神经鞘瘤:一例报告。
Ear Nose Throat J. 2023 Oct;102(10):NP527-NP533. doi: 10.1177/01455613211014103. Epub 2021 Jun 16.
4
Malignant peripheral nerve sheath tumor of nasal cavity and paranasal sinus with 13 years of follow-up-A case report and review of literature.鼻腔及鼻窦恶性外周神经鞘瘤:13年随访病例报告并文献复习
Clin Case Rep. 2019 Oct 4;7(11):2194-2201. doi: 10.1002/ccr3.2465. eCollection 2019 Nov.
5
Malignant peripheral nerve sheath tumor of the nasal cavity and nasopharynx in a child: A case report.儿童鼻腔及鼻咽部恶性外周神经鞘瘤:一例报告
Medicine (Baltimore). 2019 Jan;98(4):e14223. doi: 10.1097/MD.0000000000014223.
6
Cancer of the Peripheral Nerve in Neurofibromatosis Type 1.1型神经纤维瘤病中的周围神经肿瘤
Neurotherapeutics. 2017 Apr;14(2):298-306. doi: 10.1007/s13311-017-0518-y.
7
Malignant peripheral nerve sheath tumors of the head and neck: a case series and literature review.头颈部恶性外周神经鞘瘤:病例系列报道及文献综述
Case Rep Otolaryngol. 2014;2014:368920. doi: 10.1155/2014/368920. Epub 2014 Dec 4.
8
Malignant peripheral nerve sheath tumors: prognostic factors and survival in a series of patients treated at a single institution.恶性周围神经鞘膜瘤:单机构治疗的一系列患者的预后因素及生存情况
Cancer. 2006 Sep 1;107(5):1065-74. doi: 10.1002/cncr.22098.

鼻窦和眼眶罕见的小儿恶性外周神经鞘瘤病例

A rare Encounter with Pediatric Malignant Peripheral Nerve Sheath Tumor in Nasal Sinuses and Orbit.

作者信息

Khan Adil Aziz, Ahuja Sana, Zaheer Sufian

机构信息

Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2024 Aug;76(4):3528-3531. doi: 10.1007/s12070-024-04595-x. Epub 2024 Mar 13.

DOI:10.1007/s12070-024-04595-x
PMID:39130290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11306660/
Abstract

This case report explores a rare and aggressive Malignant Peripheral Nerve Sheath Tumor (MPNST) in a 7-year-old child affecting nasal sinuses, maxilla, and orbit, an exceptionally uncommon pediatric manifestation unrelated to Neurofibromatosis 1. The child presented with alarming symptoms-nasal obstruction, snoring, epistaxis, and difficulty swallowing-underscoring the case's urgency. Non-contrast computed tomography revealed an extensive mass infiltrating nasopharynx, nasal cavity, maxillary sinus, ethmoid sinuses, and orbit, causing destructive consequences. Histopathology confirmed a high-grade MPNST, marked by rapid growth and early metastasis, highlighting management challenges. The rarity of pediatric MPNST in the nasal cavity is discussed, emphasizing the need for a broad differential diagnosis. Treatment involves surgical resection and adjuvant chemoradiation with a grim prognosis due to diagnostic complexities and morphological mimicry in young patients.

摘要

本病例报告探讨了一名7岁儿童中罕见且侵袭性的恶性外周神经鞘瘤(MPNST),该肿瘤累及鼻窦、上颌骨和眼眶,这是一种与1型神经纤维瘤病无关的极为罕见的儿科表现。患儿出现了令人担忧的症状——鼻塞、打鼾、鼻出血和吞咽困难——凸显了该病例的紧迫性。非增强计算机断层扫描显示一个广泛的肿块浸润鼻咽、鼻腔、上颌窦、筛窦和眼眶,造成了破坏性后果。组织病理学证实为高级别MPNST,其特点是生长迅速和早期转移,突出了管理挑战。文中讨论了鼻腔小儿MPNST的罕见性,强调了进行广泛鉴别诊断的必要性。治疗包括手术切除和辅助放化疗,由于年轻患者诊断复杂且存在形态学模仿,预后严峻。