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SOLITARY RETINAL CAPILLARY HEMANGIOMA IN A PATIENT WITH BILATERAL CHORIORETINAL COLOBOMA

机译:双侧脉络膜肺瘤的患者孤独的视网膜毛细血管瘤

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Purpose: To report a case showing a very rare association of chorioretinal coloboma and retinal capillary hemangioma in a previously healthy patient. Methods: Observational case report. Results: A 21-year-old woman presented at our clinic for vision screening. She had a history of bilateral chorioretinal coloboma with amblyopia in her left eye. Her best-corrected visual acuity was 20/25 in her right eye and 20/200 in her left eye. On slit-lamp examination, iris coloboma was observed in the left eye. Fundus evaluation showed inferior chorioretinal coloboma in both eyes, and an elevated, round, and orange-red retinal lesion with feeder vessels localized in the midperipheral region of the right eye. The patient was diagnosed as having solitary retinal capillary hemangioma and underwent argon laser therapy for treating the tumoral lesion. Diagnostic studies were negative for von Hippel-Lindau disease. This is the first reported case of solitary retinal capillary hemangioma associated with bilateral chorioretinal coloboma. Conclusion: Chorioretinal coloboma is a congenital defect of the eye caused by improper closure of the embryonic fissure. Retinal capillary hemangioma is a vascular retinal tumor that may occur sporadically or as part of the von Hippel-Lindau syndrome. We report a rare association of chorioretinal coloboma and retinal capillary hemangioma in a previously healthy patient.
机译:目的:举报案例显示在先前健康的患者中具有较罕见的胆管癌团簇和视网膜毛细血管瘤的案例。方法:观察病例报告。结果:一名21岁女性在我们的诊所提供了视力筛选。她患有双侧泡草瘤的历史,左眼弱视。她的最佳矫正视力是她右眼的20/25,她的左眼20/200。在狭缝灯检查上,在左眼观察到虹膜Coloboma。眼底评估显示眼睛中的较低的脉络膜肿瘤,以及升高,圆形和橙红色视网膜病变,其具有右眼的中层区域的馈入器容器。患者被诊断为具有孤立视网膜毛细血管血肿和接受氩激光疗法的孤立性,用于治疗肿瘤病变。诊断研究对于von Hippel-Lindau病是阴性的。这是第一个报告的孤立视网膜毛细血管血管瘤的案例,与双侧脉络膜肺栓癌相关。结论:脉络膜组落瘤是胚胎裂缝闭合不当引起的眼睛的先天性缺陷。视网膜毛细血管血管瘤是一种血管视网膜肿瘤,可能偶尔发生或作为von Hippel-lindau综合征的一部分。我们在先前健康的患者中报告了胆小血肿和视网膜毛细血管和视网膜毛细血管瘤的罕见。

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