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Optic coherence tomography appearances of retinal astrocytic hamartoma and systemic features in tuberous sclerosis of Japanese patients

机译:视网膜星形胶质瘤HAMARTOMA与日本患者结核硬化神经胶质瘤的视网膜胶囊瘤和系统特征

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Purpose: To describe the optical coherence tomography findings of retinal astrocytic hamartoma of tuberous sclerosis and to confirm the association between the type of retinal astrocytic hamartoma and systemic manifestations in Japanese patients. Study Design: A retrospective observational case series. Methods: The medical records of 35 patients with tuberous sclerosis who underwent ophthalmological examination were reviewed. The retinal astrocytic hamartomas were classified into four types based on the optical coherence tomography findings, and their association with systemic disease was evaluated. Results: A total of 40 retinal astrocytic hamartomas in 13 eyes of eight patients aged 4-28 years were identified. Optical coherence tomography images were obtained for 23 lesions in 10 eyes of seven patients. Retinal astrocytic hamartomas were seen as protruding lesions of varying heights (maximum thickness, range between 221 to 1043 mu m). Of the 23, 15 lesions showed homogeneous reflectivity; in six lesions, hyper-reflective spots that presumably represented intratumoral calcification were noted. Vitreous changes were noted in 13 lesions; vitreous seeding by retinal astrocytic hamartoma was observed in seven eyes. There were no significant differences in the rates of each systemic feature among the optical coherence tomography types. Conclusion: Retinal astrocytic hamartomas were classified into four types according to the previous reports; however, this classification may be worthless because the extent of protrusion did not correspond to the intratumoral characteristics, and the involved depth of the retina was not same even in the same type. An association between the type of retinal astrocytic hamartoma and systemic manifestations was not confirmed in this small case series. We considered that the classification of retinal astrocytic hamartoma and its association with systemic manifestations need further study.
机译:目的:描述肿瘤硬化症视网膜星形胶质瘤的光学相干断层扫描结果,并确认日本患者视网膜星形胶质瘤的类型与全身表现之间的关联。研究设计:回顾性观察案例系列。方法:综述了35例患有眼科检查的肺结结核患者的病历。基于光学相干断层摄影发现,视网膜星形胶质细胞杂志族分为四种类型,并评估其与全身疾病的关联。结果:鉴定了4-28岁的8名患者13只眼睛的40例视网膜星形织物阴离子。在7名患者10只眼中获得了23个病变的光学相干断层摄影图像。视网膜星形胶质细胞瘤Hamartomas被视为不同高度的突出病变(最大厚度,221至1043μm之间的范围。在23中,15个病变显示出均匀的反射率;在六个病变中,注意到提出了可能代表妥善钙化的超反射斑点。在13个病变中注意到玻璃体的变化;在七个眼睛中观察到视网膜星形织造织物的玻璃体播种。光学相干断层扫描类型中的每个系统特征的速率没有显着差异。结论:根据上一份报告,视网膜星形胶质细胞杂志群体分为四种类型;然而,这种分类可能是毫无价值的,因为突起的程度不对应于纳米型特性,并且即使在相同类型中,视网膜的涉及深度不相同。在这个小型案例系列中没有确认视网膜星形胶质细胞瘤的类型和系统性表现之间的关联。我们认为,视网膜星形胶质细胞空间的分类及其与系统性表现的关联需要进一步研究。

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