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Multimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment Epithelium

机译:multimodale Bildgebung eines retinalen astrozyten-Hamartoms assoziert mit angeborener Hypertrophie des retinalen pigmentepithels 视网膜星形细胞错构瘤的多模态成像与先天性视网膜色素上皮肥大相关

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摘要

Hamartoma is a nodular malformation, with a single or multiple malformations, it is a recognized prenatal developmental abnormality. This benign tumor lesion has the same histological components of normal parenchyma, but these components are arranged haphazardly which disrupts normal function. Hamartomas usually remain connected with the tissue of origin; as is the case with pulmonary hamartoma or the splenic hamartoma. The exact incidence of retinal astrocytic hamartoma (RAH) is not well known, but it is estimated at one case per 100 000 births per year [1]. The astrocytic hamartoma is a neuroglial tissue and produces astrocytes within the optic nerve [2], and consequently it often appears within papillary region.
机译:Hamartoma是一种结节性畸形,具有单一或多种畸形,它是一种公认​​的产前发育异常。该良性肿瘤病变具有正常实质的相同组织学成分,但这些组分随意地布置,其破坏正常功能。海马拉斯通常与原产地组织保持联系;与肺动脉瘤或脾脏瘤的情况一样。视网膜星形胶质细胞的确切发病率(RAH)尚不熟知,但每年100 000次初生估计估计[1]。星形胶质细胞杂志是一种神经眼压组织,并在视神经中产生星形胶质细胞[2],因此它通常出现在乳头区域内。

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