额神经鞘瘤,16岁女孩,呈快速生长2年。

Surgical neurology international Pub Date : 2024-11-01 eCollection Date: 2024-01-01 DOI:10.25259/SNI_782_2024
Keisuke Murofushi, Satoshi Tsutsumi, Shigeki Tomita, Motoki Yamataka, Natsuki Sugiyama, Hideaki Ueno, Hisato Ishii
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引用次数: 0

摘要

背景:起源于额神经的眶神经鞘瘤是一种罕见但独特的肿瘤。病例描述:一名16岁女孩因渐进性脊柱突出来我院就诊。2年前的计算机断层扫描(CT)在左眼眶偶然发现一个13mm × 14mm × 10mm的球后肿块,在4岁时的CT上没有发现。发病时CT显示肿瘤生长明显,约24mm × 20mm × 17mm。在磁共振成像(MRI)上,肿瘤在T1和t2加权序列上均呈均匀等强。患者行经颅肿瘤切除术。单侧额部开颅后,左侧前窝底行截骨术。眶周反射显示额神经近端与肿瘤混在一起。提肌和上直肌被压平,位于肿瘤的正下方。行大体全切除。切除肿瘤的显微镜检查结果与神经鞘瘤一致。结论:额神经神经鞘瘤在一定条件下生长迅速。当年轻患者发现无症状的眼眶肿瘤(可能是额神经神经鞘瘤)时,建议定期随访MRI并及时切除。
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Frontal nerve schwannoma in a 16-year-old girl presenting with a rapid growth for 2 years.

Background: Orbital schwannomas arising from the frontal nerve are a rare but distinct entity.

Case description: A 16-year-old girl presented to our hospital with gradually progressive proptosis. Computed tomography (CT) performed 2 years ago incidentally detected a retrobulbar mass in the left orbit measuring 13 mm × 14 mm × 10 mm, which was not identified on CT performed at the age of 4 years. CT taken at presentation revealed marked tumor growth over 2 years, measuring 24 mm × 20 mm × 17 mm. On magnetic resonance imaging (MRI), the tumor appeared homogeneously isointense both on the T1- and T2-weighted sequences. The patient underwent transcranial tumor resection. Following unilateral frontal craniotomy, an osteotomy was made to the left anterior fossa floor. On reflecting, the periorbita revealed the frontal nerve with the proximal segment intermingled with the tumor. The levator and superior rectus muscles were flattened and located immediately beneath the tumor. A gross total resection was performed. Microscopic findings of the resected tumor were consistent with schwannoma.

Conclusion: Frontal nerve schwannomas may grow rapidly under certain conditions. Periodic follow-up using MRI and timely resection is recommended when an asymptomatic orbital tumor, possibly a frontal nerve schwannoma, is detected in young patients.

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