Evidence map›Paper›PMID 26584552›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2016

Posterior reversible encephalopathy syndrome (PRES): a rare condition after resection of posterior fossa tumors: two new cases and review of the literature.

Lain Hermes González Quarante, José Hinojosa Mena-Bernal, Beatriz Pascual Martín, Marta Ramírez Carrasco, María Jesús Muñoz Casado, Ana Martínez de Aragón, Rogelio Simón de las Heras

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In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Lain Hermes González QuaranteDepartment of Pediatric Neurosurgery, Hospital General 12 de Octubre, Madrid, Spain. lainhermesgq@gmail.com.
José Hinojosa Mena-BernalDepartment of Pediatric Neurosurgery, Hospital General 12 de Octubre, Madrid, Spain.
Beatriz Pascual MartínDepartment of Pediatric Neurosurgery, Hospital General 12 de Octubre, Madrid, Spain.
Marta Ramírez CarrascoDepartment of Pediatric Neurosurgery, Hospital General 12 de Octubre, Madrid, Spain.
María Jesús Muñoz CasadoDepartment of Pediatric Neurosurgery, Hospital General 12 de Octubre, Madrid, Spain.
Ana Martínez de AragónDepartment of Neuroradiology, Hospital General 12 de Octubre, Madrid, Spain.
Rogelio Simón de las HerasDepartment of Pediatric Neurology, Hospital General 12 de Octubre, Madrid, Spain.
Research Institute Hospital 12 de Octubre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn 1996, Hinchey and colleagues coined the term "Posterior reversible encephalopathy syndrome" (PRES) to describe a condition seen in patients with acute neurological symptoms and reversible subcortical vasogenic edema predominantly involving parieto-occipital areas demonstrated in brain MRI. The occurrence of this phenomenon after surgical resection of CNS tumors is typically linked to pediatric cases. MATERIAL AND

methodsTwo new cases of PRES after posterior fossa surgery are reported. A thorough review of the literature is carried out with the purpose of updating and summarizing the main features regarding PRES in similar cases. Seven cases of PRES after resection of a posterior fossa tumor have been hitherto reported (4 patients were <20 years old). There is another pediatric case described after a ventriculoperitoneal shunting procedure in a patient with fourth ventricle ependymoma. Two resected tumors were ependymomas, 2 hemangiopericytomas in one patient, 1 pilocyticastrocytoma, 1 vestibular schwannoma, and 1 of the reported cases did not describe the final pathology diagnosis. CASE REPORTS: We present 2 new cases of PRES after surgical resection of a posterior fossa tumor (medulloblastoma in case 1 and ependymoma in case 2) in pediatric patients. Case 1 developed delayed seizures and altered mental status(10 days after surgical resection) after receiving treatment with bromocriptine for cerebellar mutism. Case 2 presented with generalized seizures and altered mental status within the first 48 postoperative hours followed by right hemiparesis. Both patients fully recovered and returned to neurological baseline status. A thorough review of the literature was carried out with the purpose of updating and summarizing the main features regarding PRES in similar cases.

conclusionsWe report 2 new pediatric cases of posterior reversible encephalopathy syndrome (PRES) that developed after surgical resection of a posterior fossa tumor. Appropriate management includes supportive measures, antihypertensive agents, and antiepileptic drugs, if needed. Full recovery is the most likely outcome in line with previous articles.

Indexed as

AdolescentChild, PreschoolHumansInfratentorial NeoplasmsMagnetic Resonance ImagingMaleMedulloblastomaNeurosurgical ProceduresPosterior Leukoencephalopathy SyndromeTreatment OutcomeEpendymomaMedulloblastomaPosterior fossa surgeryPosterior reversible encephalopathy syndromePRES

Identifiers

PMID26584552
OpenAlexW2174712973

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.