Rao P Kumar, Almony Arghavan, Shah Gaurav K, Cooper Blake, Smith Morton E
From the *Department of Ophthalmology & Visual Sciences, Washington University School of Medicine, St. Louis; †Barnes Retina Institute, St. Louis, MO; and ‡University of Kansas Hospital, Kansas City.
Retin Cases Brief Rep. 2009 Winter;3(1):60-1. doi: 10.1097/ICB.0b013e31815654ca.
To report the histologic and immunohistochemical features of a congenital vitreous cyst.
Interventional case report with immunohistochemical correlation. A 58-year-old woman with known vitreous cyst since childhood had an enlarging visual floater. The vitreous cyst was removed by pars plana vitrectomy and central vision was restored.
Pathology confirmed a vitreous cyst derived from neural and glial tissue and consistent with retinal origin.
Congenital vitreous cysts, derived from neural and glial tissue, can be safely removed using pars plana vitrectomy.
报告先天性玻璃体囊肿的组织学和免疫组化特征。
伴有免疫组化相关性的介入性病例报告。一名自童年起就已知患有玻璃体囊肿的58岁女性出现了视力模糊且逐渐加重的飞蚊症。通过玻璃体切除术切除玻璃体囊肿后，中心视力得以恢复。
病理学证实该玻璃体囊肿源自神经和神经胶质组织，与视网膜起源相符。
源自神经和神经胶质组织的先天性玻璃体囊肿可通过玻璃体切除术安全切除。
