Posterior reversible encephalopathy syndrome in preeclampsia

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Late postpartum preeclampsia with posterior reversible encephalopathy syndrome.

Posterior reversible encephalopathy syndrome is a reversible syndrome characterized by headache, seizures, altered mentation, and loss of vision associated with white matter changes on imaging. We report here a 27 year-old lady three weeks postpartum, presenting with posterior reversible encephalopathy syndrome. She was treated successfully with antihypertensives and showed dramatic improvement...

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Posterior reversible encephalopathy syndrome.

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Posterior reversible encephalopathy syndrome.

Posterior reversible encephalopathy syndrome (PRES) is characterized by headache, altered mental status, visual disturbances, and seizures. Radiological features typically include edema of the posterior cerebral regions, especially of the parietooccipital lobes. Atypical imaging features, such as involvement of anterior cerebral regions, deep white matter, and the brain stem are also frequently...

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Posterior reversible encephalopathy syndrome.

Posterior reversible encephalopathy syndrome (PRES) is a clinico-neuro-radiological entity may develop in patients with pre-eclampsia, eclampsia or delayed postpartum eclampsia, immunological conditions and with certain anti-neoplastic agents. This case report describes about a patient with pregnancy induced hypertension who developed PRES postnatally. Early recognition and treatment prevented ...

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Posterior reversible encephalopathy syndrome (PRES).

Posterior reversible encephalopathy syndrome (PRES) is a clinicoradiologic entity. Neurotoxicity with characteristic watershed CT/MR imaging features characterize this condition. This case report describes PRES syndrome in a 35-year-old patient admitted with eclampsia. On the first postpartum day; she developed severe headache, generalized tonic-clonic seizures and visual symptoms including tr...

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ژورنال

عنوان ژورنال: International Journal of Reproduction, Contraception, Obstetrics and Gynecology

سال: 2019

ISSN: 2320-1789,2320-1770

DOI: 10.18203/2320-1770.ijrcog20196048