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小儿眶神经鞘瘤的非典型、极快速生长。

Atypical, Extremely Rapid Growth of Pediatric Orbital Neurilemmoma.

机构信息

Adnexal Service, Moorfields Eye Hospital.

Department of Eye Pathology, UCL Institute of Ophthalmology, London, United Kingdom.

出版信息

Ophthalmic Plast Reconstr Surg. 2021;37(5):e164-e167. doi: 10.1097/IOP.0000000000001958.

DOI:10.1097/IOP.0000000000001958
PMID:33710033
Abstract

Solitary orbital neurilemmoma-a benign tumor of Schwann cells in a peripheral nerve-sheath-are typically very slow growing and present in middle age; in the absence of neurofibromatosis, they are almost never seen in childhood. We describe the clinical presentation, imaging, pathology, and management of this tumor in a 12 years old-the tumor growing extremely rapidly over 5 months and without any evidence of cystic degeneration, hemorrhage, or sarcomatous features. The possibility of tumor growth having been accelerated by prior biopsy is discussed.

摘要

孤立性眶内神经鞘瘤——一种发生于外周神经鞘的施万细胞良性肿瘤——通常生长非常缓慢,见于中年;在无神经纤维瘤病的情况下,在儿童中几乎从未见过。我们描述了一例 12 岁患儿的临床表现、影像学表现、病理学和治疗方法,肿瘤在 5 个月内迅速生长,没有任何囊性变性、出血或肉瘤样特征的证据。讨论了先前活检加速肿瘤生长的可能性。

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引用本文的文献

1
Frontal nerve schwannoma in a 16-year-old girl presenting with a rapid growth for 2 years.一名16岁女孩患有额神经鞘瘤,肿瘤在2年内迅速生长。
Surg Neurol Int. 2024 Nov 1;15:400. doi: 10.25259/SNI_782_2024. eCollection 2024.
2
Pediatric dumbbell-shaped orbital schwannoma with extension to the cranial cavity: A case report and literature review.小儿哑铃形眼眶神经鞘瘤向颅腔扩展:1例报告及文献复习
Front Neurol. 2023 Jan 10;13:1071632. doi: 10.3389/fneur.2022.1071632. eCollection 2022.