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Choroidal Detachment and Increased Intraocular Pressure in a Case of Secondary Pulmonary Hypertension

机译:在继发性肺动脉高压的情况下脉络膜脱离和口腔内压增加

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Purpose: To report a case of secondary pulmonary hypertension, choroidal detachment, and increased intraocular pressure (IOP) in a patient with a congenital ventricular septal defect. Methods: This is a case report. Patient: A 36-year-old man with congenital ventricular septal defect developed dilated and congested conjunctival and episcleral veins, high IOP, and choroidal detachment. Results: The right eye had secondary glaucoma, myopia, and choroidal detachment. He had severe pulmonary hypertension and decreased heart function. After successful treatment for heart failure, IOP was reduced, the refractive state returned to normal, choroidal detachment was reversed, and visual acuity improved. Conclusions: Secondary pulmonary hypertension resulting from a congenital ventricular septal defect caused serious optic abnormalities that resolved substantially with appropriate treatment of the pulmonary hypertension.
机译:目的:报告具有先天性心室间隔缺损的患者中患有次级肺动脉高压,脉络膜脱离,脉络膜脱离和增加的眼压(IOP)的情况。 方法:这是一个案例报告。 患者:一名36岁男性,先天性室间隔缺损发育扩张和拥挤的结膜和椎间静脉,高IOP和脉络膜脱离。 结果:右眼具有二级青光眼,近视和脉络膜脱离。 他患有严重的肺动脉高压和心脏功能下降。 成功治疗心力衰竭后,IOP降低,恢复到正常,脉络膜脱离恢复的折射状态,视力改善。 结论:由先天性室间隔缺损引起的继发性肺动脉高压导致严重的光学异常,其基本上通过适当治疗肺动脉高压治疗。

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