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子痫前期的急性皮质盲——一例可逆性后部脑病综合征病例

Acute cortical blindness in preeclampsia--a case of reversible posterior encephalopathy syndrome.

作者信息

Mitas Leszek, Rogulski Lech

机构信息

Oddział Połozniczo-Ginekologiczny, Wojewódzki Szpital Specjalistyczny w Czestochowie, Polska.

出版信息

Ginekol Pol. 2012 Jun;83(6):469-72.

Abstract

BACKGROUND

Cortical blindness is one the most disturbing symptoms of reversible posterior encephalopathy syndrome in preeclamptic and eclamptic patients. The disease has been previously associated with a hypertensive breakthrough in the autoregulation of posterior cerebral arterioles followed by extravasation of the fluid into the brain tissue.

CASE

22-year-old primigravida in the 39th week of gestation diagnosed with gestational diabetes mellitus presented with mild preeclampsia and was admitted to our hospital. Antihypertensive treatment was initiated. Her blood pressure remained between 120/80 to 140/90 mm Hg. Glucose levels were within acceptable range. Before the labor induction she developed acute cortical blindness. Magnetic resonance imaging showed vasogenic edema localized in occipital lobes. Cesarean section was performed and anti-edematous treatment initiated. Blindness resolved by the fifth day postpartum.

CONCLUSIONS

Reversible posterior encephalopathy developed in our patient in spite of normalized blood pressure that remained within autoregulation limits. Alternative pathogenesis and precipitating factors are discussed.

摘要

背景

皮质盲是先兆子痫和子痫患者可逆性后部脑病综合征最令人不安的症状之一。该疾病此前被认为与大脑后小动脉自动调节功能的高血压突破有关,随后液体渗入脑组织。

病例

一名22岁初产妇,孕39周,诊断为妊娠期糖尿病,伴有轻度先兆子痫,入住我院。开始进行降压治疗。她的血压维持在120/80至140/90毫米汞柱之间。血糖水平在可接受范围内。在引产之前,她出现了急性皮质盲。磁共振成像显示枕叶存在血管源性水肿。进行了剖宫产并开始抗水肿治疗。产后第五天失明症状消失。

结论

尽管患者血压恢复正常且保持在自动调节范围内,但仍发生了可逆性后部脑病。文中讨论了其他发病机制和诱发因素。

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