原发性玻璃体囊肿。

GMS ophthalmology cases Pub Date : 2020-04-02 eCollection Date: 2020-01-01 DOI:10.3205/oc000145
Pieter Robben, Rita Van Ginderdeuren, Daphne Thoma, Catherine Deghislage, Joachim Van Calster, Johan Blanckaert, Ingele Casteels
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摘要

目的:报告2例玻璃体囊肿的病理生理及治疗方法。方法:采用眼底摄影、超声、光学相干断层扫描进行临床检查。第一例患者行组织病理学检查。结果:第一个病例是一个色素沉着、自由漂浮的囊肿,在27号玻璃体切除术中被切除。组织病理学显示单层色素上皮,证实了先前报道的pas阳性基底膜的存在。第二例为无底无色素囊肿,伴明显的屈光参差。结论:原发性玻璃体囊肿罕见,临床表现广泛。这可能反映了它们是起源于色素上皮还是原代透明体系统。玻璃体囊肿的治疗大多是保守的,但如果症状使人虚弱,则可以安全地进行玻璃体切除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Primary vitreous cysts.

Objective: To report two cases of vitreous cysts with discussion of their pathophysiology and management. Methods: Clinical examination with fundus photography, ultrasound and optical coherence tomography. Histopathology was performed in the first case. Results: The first case illustrates a pigmented, free-floating cyst, which was removed during a 27-gauge vitrectomy. The histopathology shows a single layer of pigmented epithelium and confirms the previously reported presence of a PAS-positive basement membrane. The second case shows a sessile, non-pigmented cyst associated with significant anisometropia. Conclusion: Primary vitreous cysts are rare and can have a wide range in their clinical aspect. This likely reflects whether they originate either from the pigment epithelium or the primary hyaloidal system. The management of vitreous cysts is mostly conservative, but pars plana vitrectomy can be used safely if the symptoms are debilitating.

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