首页> 美国卫生研究院文献>Saudi Journal of Ophthalmology >Orbital tumor associated with a microphthalmic eye and colobomatous cleft: Pilocytic astrocytoma (glioma) or massive retinal gliosis
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Orbital tumor associated with a microphthalmic eye and colobomatous cleft: Pilocytic astrocytoma (glioma) or massive retinal gliosis

机译:与小眼和眼球裂相关的眼眶肿瘤:上皮星形细胞瘤(神经胶质瘤)或大面积视网膜胶质增生

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摘要

A 11-year-old boy with congenital microphthalmos of the right eye presented with gradual protrusion of his ocular prosthesis. MRI showed an orbital mass adjacent to the microphthalmic eye. After removal of the eye and the orbital soft tissue mass a gliotic mass, resembling a pilocytic astrocytoma WHO grade 1 (glioma) was diagnosed. Through a colobomatous cleft in the eye the tumour spread in the orbit. There were no clinical signs of neurofibromatosis 1. This case showed a very rare association between a microphthalmic and colobomatous eye and pilocytic astrocytoma, grade 1. However a far advanced and infiltrative massive retinal gliosis cannot be definitively excluded as differential diagnosis.
机译:一个11岁的男孩,右眼先天性微眼球呈现假眼逐渐突出。 MRI显示邻近小眼的眼眶肿块。摘除眼球和眼眶软组织肿块后,诊断为神经胶质样肿块,类似于WHO 1级胶质细胞星形细胞瘤(神经胶质瘤)。通过眼球状裂口,肿瘤在眼眶内扩散。没有神经纤维瘤病1的临床体征。该病例显示,小眼和大球状眼与1级毛细胞性星形细胞瘤之间的联系非常罕见。但是,不能明确排除高度晚期和浸润性大块视网膜胶质增生作为鉴别诊断。

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