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伴有全层黄斑裂孔的先天性视网膜色素上皮单纯性错构瘤

Congenital simple hamartoma of the retinal pigment epithelium with a full-thickness macular hole.

作者信息

Van de Moere Ann, Clark J Ben

机构信息

From the Department of Ophthalmology, St. John of God Hospital, Geelong, Victoria, Australia.

出版信息

Retin Cases Brief Rep. 2009 Winter;3(1):80-2. doi: 10.1097/ICB.0b013e318158de64.

Abstract

BACKGROUND

Congenital simple hamartoma of the retinal pigment epithelium (CSHRPE) is a rare tumor that, to our knowledge, has not been previously reported as being associated with a full-thickness macular hole.

METHODS

We report a case of a CSHRPE associated with a full-thickness macular hole. Findings of funduscopy and optical coherence tomography are described.

RESULTS

A 10-year-old boy presented with visual acuity of 20/80 in the right eye. Funduscopy revealed a juxtafoveal pedunculated, well-circumscribed, darkly pigmented lesion measuring one third of a disk diameter. There was an associated full-thickness macular hole that separated the main dark mass nasally from a linear pigmented lesion. Optical coherence tomography showed a mass with optical shadowing and confirmed the presence of a full-thickness macular hole surrounded by intraretinal cystic edema. No evidence of a posterior vitreous detachment or significant epiretinal membrane was seen.

CONCLUSION

We observed a full-thickness macular hole with a CSHRPE in a 10-year-old boy. The CSHRPE may have induced tangential traction along the posterior hyaloid or abnormal anteroposterior traction with foveal dehiscence. It is possible that exudation from the lesion into the vitreous cavity may result in vitreous changes with premature liquefaction and degenerative alterations that may induce abnormal vitreous adhesion and traction. Optical coherence tomography did not show evidence of such changes.

摘要

背景

视网膜色素上皮先天性单纯性错构瘤(CSHRPE)是一种罕见肿瘤,据我们所知,此前尚无与全层黄斑裂孔相关的报道。

方法

我们报告一例与全层黄斑裂孔相关的CSHRPE病例。描述了眼底镜检查和光学相干断层扫描的结果。

结果

一名10岁男孩右眼视力为20/80。眼底镜检查发现一个位于黄斑旁的有蒂、边界清晰、色素沉着深的病变,直径为视盘直径的三分之一。伴有一个全层黄斑裂孔,将主要的深色肿物与鼻侧的线性色素沉着病变分隔开。光学相干断层扫描显示一个有光学阴影的肿物,并证实存在一个被视网膜内囊样水肿包围的全层黄斑裂孔。未发现玻璃体后脱离或明显视网膜前膜的证据。

结论

我们在一名10岁男孩中观察到一个伴有CSHRPE的全层黄斑裂孔。CSHRPE可能沿后玻璃体膜产生切线牵引或因黄斑裂开产生异常的前后牵引。病变向玻璃体腔的渗出可能导致玻璃体变化,伴有过早液化和退行性改变,进而可能导致异常的玻璃体粘连和牵引。光学相干断层扫描未显示此类变化的证据。

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