Title of article
Posterior Reversible Encephalopathy Syndrome in Pediatric Hematologic- Oncologic Disease: Literature Review and Case Presentation
Author/Authors
ARZANIAN، Mohammad Thaghi نويسنده Pediatric Congenital Hematologic Disorders Research Center, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran , , Shamsian، Bibi-Shahin نويسنده , , Karimzadeh، Parvaneh نويسنده , , KAJIYAZDI، Mohammad نويسنده Pediatric Congenital Hematologic Disorders Research Center, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran , , MALEK، Fatima نويسنده Pediatric Congenital Hematologic Disorders Research Center, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran , , HAMMOUD، Mohammad نويسنده Pediatric Congenital Hematologic Disorders Research Center, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran ,
Issue Information
فصلنامه با شماره پیاپی سال 2014
Pages
10
From page
1
To page
10
Abstract
Objective
Posterior reversible encephalopathy syndrome (PRES) is a cliniconeuroradiological
disease entity, which is represented by characteristic
magnetic resonance imaging (MRI) findings of subcortical/cortical
hyperintensity in T2-weighted sequences. It is more often seen in parietaloccipital
lobes, and is accompanied by clinical neurological changes. PRES is
a rare central nervous system (CNS) complication in patients with childhood
hematologic-oncologic disese and shows very different neurological symptoms
between patients, ranging from numbness of extremities to generalized seizure.
In this article, we will review PRES presentation in hematologic-oncologic
patients. Then, we will present our patient, a 7-year-old boy with Evans syndrome
on treatment with cyclosporine, mycophenolate mofetil (MMF) and prednisone,
with seizure episodes and MRI finding in favour of PRES.
Journal title
Iranian Journal of Child Neurology (IJCN)
Serial Year
2014
Journal title
Iranian Journal of Child Neurology (IJCN)
Record number
2281155
Link To Document