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一名患有自闭症和CHARGE综合征的儿童出现双侧小眼畸形并伴有单侧上方囊肿。

Bilateral microphthalmos with unilateral superior cyst in a child with autism and CHARGE syndrome.

作者信息

Pushker Neelam, Tinwala Sana, Khurana Saurbhi, Sen S

机构信息

Oculoplasty, Orbit & Oncology Services, Dr. Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Int Ophthalmol. 2013 Apr;33(2):195-8. doi: 10.1007/s10792-012-9653-y. Epub 2012 Oct 31.

Abstract

A case of autism with CHARGE syndrome with microphthalmos and a superior colobomatous cyst arising from the optic disc is reported. A 7-year-old boy presented with a gradually increasing mass, involving the superior orbit and upper eyelid of right eye of 3 years' duration. Clinical examination revealed bilateral microphthalmos with typical iris coloboma, posterior synechiae, and cataractous lens. Imaging revealed bilateral optic disc colobomas with a superior cyst in the right orbit. Intraoperatively, a single cystic lesion was seen in the superior orbit arising from the optic disc region. Histopathology was suggestive of a colobomatous cyst, positive for glial tissue [glial fibrillary acidic protein (GFAP) positive] and neuroretinal elements (synaptophysin positive) on immunohistochemistry. Genetic analysis revealed a normal karyotype (46, XY).

摘要

报告了一例患有CHARGE综合征的自闭症病例,该病例伴有小眼畸形以及起源于视盘的上睑裂囊肿。一名7岁男孩出现逐渐增大的肿物,累及右眼上眼眶和上眼睑,病程3年。临床检查发现双侧小眼畸形,伴有典型的虹膜缺损、虹膜后粘连和晶状体混浊。影像学检查显示双侧视盘缺损,右侧眼眶有一个上囊肿。手术中,在上眼眶可见一个起源于视盘区域的单个囊性病变。组织病理学提示为睑裂囊肿,免疫组织化学显示神经胶质组织呈阳性(胶质纤维酸性蛋白[GFAP]阳性),神经视网膜成分呈阳性(突触素阳性)。基因分析显示核型正常(46, XY)。

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