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无神经纤维瘤病情况下的局限性双侧眶上及眶下神经纤维瘤

Localized Bilateral Superior and Inferior Orbital Neurofibroma in the Absence of Neurofibromatosis.

作者信息

Rojas-Correa Daniela, Bengoa-González Álvaro, Mencía-Gutiérrez Enrique, Hernández-Laín Aurelio, Salvador Elena, Martín-Clavijo Agustín, Jiménez-Almonacid Justino, Lago-Llinás María-Dolores

机构信息

Ophthalmology Department, 12 de Octubre Hospital, Complutense University, 28041 Madrid, Spain.

Neuropathology Department, 12 de Octubre Hospital, Complutense University, 28041 Madrid, Spain.

出版信息

Case Rep Ophthalmol Med. 2021 Jun 4;2021:6655134. doi: 10.1155/2021/6655134. eCollection 2021.

Abstract

Localized or isolated neurofibromas are peripheral nerve sheath tumors. They are rare in the orbit and occur without a systemic neurofibromatosis. There are few cases of bilateral tumors reported but none affecting both supraorbital and infraorbital nerves. We report a 45-year-old female who presented an extraconal mass in the right orbit as an incidental finding in a head computer tomography, without ocular symptoms. Magnetic resonance image showed a well-defined oval mass in the right supraorbital and infraorbital nerves, of similar characteristics, as well as smaller masses in the left supraorbital and infraorbital nerves. A progressive increase in size of the left supraorbital and infraorbital tumor motivated their surgical excision. The histological result was compatible with a neurofibroma. These uncommon orbital tumors are slow growing and affect the sensory nerves of the trigeminal nerve. Neurofibromas usually present progressive symptoms due to the orbital mass, proptosis, or visual changes although not in this case. Surgical removal is the only definitive treatment.

摘要

局限性或孤立性神经纤维瘤是周围神经鞘瘤。它们在眼眶中罕见,且在无系统性神经纤维瘤病的情况下发生。双侧肿瘤的报道很少,且尚无累及眶上神经和眶下神经两者的病例。我们报告一名45岁女性,其在头部计算机断层扫描中偶然发现右侧眼眶有一个眶外肿块,无眼部症状。磁共振成像显示右侧眶上神经和眶下神经有一个边界清晰的椭圆形肿块,特征相似,左侧眶上神经和眶下神经也有较小的肿块。左侧眶上神经和眶下神经肿瘤大小逐渐增大,促使对其进行手术切除。组织学结果与神经纤维瘤相符。这些罕见的眼眶肿瘤生长缓慢,影响三叉神经的感觉神经。神经纤维瘤通常因眼眶肿块、眼球突出或视力改变而出现进行性症状,不过本例并非如此。手术切除是唯一的确定性治疗方法。

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