搏动性眼球内陷是1型神经纤维瘤病的首发症状。

Beyoglu Eye Journal Pub Date : 2025-03-25 eCollection Date: 2025-01-01 DOI:10.14744/bej.2025.33341
Aslihan Yilmaz Cebi, Bilge Batu Oto, Oguzhan Kilicarslan, Ahmet Murat Sarici
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引用次数: 0

摘要

我们报告1型神经纤维瘤病(NF-1)患者搏动性眼球内陷为第一症状。一名25岁女性因左眼后侧移位和头痛向我们就诊。患者眼球内陷伴搏动。裂隙灯检查显示双侧Lisch结节,眼眶计算机断层扫描显示左侧蝶骨大翼发育不全。患者有卡萨梅-奥莱斑疹,脊柱侧凸史,脾切除手术。遗传咨询证实了NF-1的诊断。NF-1是一种多系统、常染色体显性遗传病,具有皮肤、神经、心血管和眼科表现。肿瘤抑制基因NF-1功能障碍是主要原因。因此,定期筛查肿瘤的发展是必要的。由于NF-1有几种神经眼科表现,眼科医生可以在其诊断和治疗中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulsating Enophthalmos as an Initial Symptom of Neurofibromatosis Type 1.

We report a neurofibromatosis type 1 (NF-1) patient with pulsating enophthalmos as the first symptom. A 25-year-old female presented to us with posterior displacement of the left eye and a headache. The patient had enophthalmos with pulsations. A slit lamp examination revealed bilateral Lisch nodules and a computed tomography scan of the orbit demonstrated aplasia of the greater wing of the sphenoid bone on the left. The patient had café-au-lait macules, a history of scoliosis, and splenectomy operations. Genetic counseling confirmed the diagnosis of NF-1. NF-1 is a multisystemic, autosomal dominant genetic disease with cutaneous, neurologic, cardiovascular, and ophthalmologic manifestations. Dysfunction of tumor suppressor gene NF-1 is the main cause. Therefore, periodic screening for tumor development is required. Since NF-1 has several neuro-ophthalmological findings, ophthalmologists can play a significant role in its diagnosis and management.

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