Juniat Valerie, Patel Sandy, Davis Garry, Crompton John L, Selva Dinesh
South Australian Institute of Ophthalmology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
Department of Medical Imaging, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
Neuroophthalmology. 2020 May 1;44(6):395-398. doi: 10.1080/01658107.2020.1746361. eCollection 2020.
Optic nerve choristomas are very rare lesions. They are characterised by the presence of fat cells, mesodermal collection of fibrous tissue and smooth muscle, and atrophic optic nerve tissue. Although the condition can be diagnosed on histology, it is not always possible to carry out surgical exploration for tissue diagnosis in view of the apical location of the lesion and the inherent risk to vision from surgery. Detailed neuro-imaging becomes vital in these cases for diagnosis. We report a case of a patient with an optic nerve choristoma diagnosed on neuroimaging, review the current literature related to this condition, and discuss the key clinico-radiological features of optic nerve choristomas.
视神经迷离瘤是非常罕见的病变。其特征是存在脂肪细胞、纤维组织和平滑肌的中胚层集合,以及萎缩的视神经组织。尽管这种情况可通过组织学诊断,但鉴于病变的顶端位置以及手术对视力的固有风险,并不总是能够进行手术探查以进行组织诊断。在这些病例中,详细的神经影像学检查对于诊断至关重要。我们报告一例经神经影像学诊断为视神经迷离瘤的患者,回顾与该疾病相关的当前文献,并讨论视神经迷离瘤的关键临床放射学特征。