Posterior reversible encephalopathy syndrome– our experience

Introduction: Posterior Reversible Encephalopathy syndrome (PRES) is an emergency medical condition with varied etiology, presentation and outcome reported in literature. The objective of this study was to determine the clinical and radiological presentations, and clinical outcomes in cases of PRES...

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Main Authors: Sravya VV Kotaru, Pravin Naphade, Shalesh Rohatgi, Satish Nirhale, Prajwal Rao, Dhaval Dave, Akram Furqan Mohd Khan, Sahil BK Gupta
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2021-01-01
Series:Medical Journal of Dr. D.Y. Patil Vidyapeeth
Subjects:
Online Access:http://www.mjdrdypv.org/article.asp?issn=2589-8302;year=2021;volume=14;issue=5;spage=486;epage=491;aulast=Kotaru
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spelling doaj-381fa5a9ae5d4d0da5ca5ebbba4788ab2021-09-08T03:51:50ZengWolters Kluwer Medknow PublicationsMedical Journal of Dr. D.Y. Patil Vidyapeeth2589-83022589-83102021-01-0114548649110.4103/mjdrdypu.mjdrdypu_262_20Posterior reversible encephalopathy syndrome– our experienceSravya VV KotaruPravin NaphadeShalesh RohatgiSatish NirhalePrajwal RaoDhaval DaveAkram Furqan Mohd KhanSahil BK GuptaIntroduction: Posterior Reversible Encephalopathy syndrome (PRES) is an emergency medical condition with varied etiology, presentation and outcome reported in literature. The objective of this study was to determine the clinical and radiological presentations, and clinical outcomes in cases of PRES admitted over the last one year at a tertiary care hospital. Materials and Methods: We retrospectively analysed all cases diagnosed with PRES from May 2019 to May 2020. We reviewed clinical presentations, etiological history, imaging characteristics, management and clinical outcomes. Results: Five patients diagnosed with PRES were identified. All patients were females, with age range between 16 to 32 years. Etiological factors were eclampsia (2/5), drug (tacrolimus), massive blood transfusion and chronic kidney disease with hypertension. Headache was the most common clinical presentation. Other clinical presentations were visual symptoms, seizures, altered sensorium, vertigo and vomiting. The most common imaging characteristic was supratentorial T2/FLAIR white matter hyperintensity on MRI, predominantly in parieto-occipital region. Other areas of white matter involvement were cerebellum and brainstem. One patient had hemorrhage complicating PRES. All patients were primarily managed by elimination and treatment of the precipitating factors, along with standard anti-oedema measures and anti-epileptic drugs. There was complete recovery in all patients within one week. Conclusion: PRES has variable clinical and radiological presentation. Early diagnosis and elimination of precipitating factors are vital for complete recovery.http://www.mjdrdypv.org/article.asp?issn=2589-8302;year=2021;volume=14;issue=5;spage=486;epage=491;aulast=Kotaruposterior reversible encephalopathy syndromevasogenic brain oedemahypertension
collection DOAJ
language English
format Article
sources DOAJ
author Sravya VV Kotaru
Pravin Naphade
Shalesh Rohatgi
Satish Nirhale
Prajwal Rao
Dhaval Dave
Akram Furqan Mohd Khan
Sahil BK Gupta
spellingShingle Sravya VV Kotaru
Pravin Naphade
Shalesh Rohatgi
Satish Nirhale
Prajwal Rao
Dhaval Dave
Akram Furqan Mohd Khan
Sahil BK Gupta
Posterior reversible encephalopathy syndrome– our experience
Medical Journal of Dr. D.Y. Patil Vidyapeeth
posterior reversible encephalopathy syndrome
vasogenic brain oedema
hypertension
author_facet Sravya VV Kotaru
Pravin Naphade
Shalesh Rohatgi
Satish Nirhale
Prajwal Rao
Dhaval Dave
Akram Furqan Mohd Khan
Sahil BK Gupta
author_sort Sravya VV Kotaru
title Posterior reversible encephalopathy syndrome– our experience
title_short Posterior reversible encephalopathy syndrome– our experience
title_full Posterior reversible encephalopathy syndrome– our experience
title_fullStr Posterior reversible encephalopathy syndrome– our experience
title_full_unstemmed Posterior reversible encephalopathy syndrome– our experience
title_sort posterior reversible encephalopathy syndrome– our experience
publisher Wolters Kluwer Medknow Publications
series Medical Journal of Dr. D.Y. Patil Vidyapeeth
issn 2589-8302
2589-8310
publishDate 2021-01-01
description Introduction: Posterior Reversible Encephalopathy syndrome (PRES) is an emergency medical condition with varied etiology, presentation and outcome reported in literature. The objective of this study was to determine the clinical and radiological presentations, and clinical outcomes in cases of PRES admitted over the last one year at a tertiary care hospital. Materials and Methods: We retrospectively analysed all cases diagnosed with PRES from May 2019 to May 2020. We reviewed clinical presentations, etiological history, imaging characteristics, management and clinical outcomes. Results: Five patients diagnosed with PRES were identified. All patients were females, with age range between 16 to 32 years. Etiological factors were eclampsia (2/5), drug (tacrolimus), massive blood transfusion and chronic kidney disease with hypertension. Headache was the most common clinical presentation. Other clinical presentations were visual symptoms, seizures, altered sensorium, vertigo and vomiting. The most common imaging characteristic was supratentorial T2/FLAIR white matter hyperintensity on MRI, predominantly in parieto-occipital region. Other areas of white matter involvement were cerebellum and brainstem. One patient had hemorrhage complicating PRES. All patients were primarily managed by elimination and treatment of the precipitating factors, along with standard anti-oedema measures and anti-epileptic drugs. There was complete recovery in all patients within one week. Conclusion: PRES has variable clinical and radiological presentation. Early diagnosis and elimination of precipitating factors are vital for complete recovery.
topic posterior reversible encephalopathy syndrome
vasogenic brain oedema
hypertension
url http://www.mjdrdypv.org/article.asp?issn=2589-8302;year=2021;volume=14;issue=5;spage=486;epage=491;aulast=Kotaru
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