Optic nerve haemangioblastoma in association with von Hippel-Lindau syndrome: case report and literature review

被引:3
|
作者
Montoya, Juan David Vasquez [1 ]
Velez, Jorge Mario [2 ]
Vanegas, Melisa Naranjo [2 ]
Jimenez, Natalia Montes [2 ,3 ]
机构
[1] Univ CES, Sch Med, Medellin 085006, Colombia
[2] Biosci Ctr, Med imagine & Hlth SURA, Med Imagine & Hlth SURA, Medellin 050015, Colombia
[3] Ayudas Diagnost SURA, Biosci Ctr, Carrera 4826A-50,Third floor, Medellin 050015, Colombia
来源
BJR CASE REPORTS | 2024年 / 10卷 / 02期
关键词
haemangioblastoma; optic nerve; von Hippel-Lindau syndrome; case reports; DISEASE; TUMORS;
D O I
10.1093/bjrcr/uaae007
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Optic nerve haemangioblastoma (ONH) is an uncommon, benign, non-meningothelial, mesenchymal tumour of unclear origin. Most are associated with von Hippel-Lindau (VHL) syndrome (71%), and only 40 cases have been reported in the medical literature. Most of the patients develop non-specific visual symptoms, including decreased visual acuity and/or loss of visual fields, exophthalmos, trigeminal neuralgia, and retroorbital pain. Optic nerve sheath meningioma and optic nerve glioma are among the differential diagnoses that may be considered in this location. Contrast-enhanced MRI is considered an optimal diagnostic tool, which helps to determine some characteristics that guide towards an adequate diagnosis and treatment. We present a 42-year-old patient with a history of VHL syndrome in whom a cerebellar lesion and optic nerve lesions were evidenced, and we did a review of the literature and case analysis.
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页数:5
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