Evidence map›Paper›PMID 34623468›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2022

Medulloblastoma and esthesioneuroblastoma in a pediatric patient: a co-incidence or result of common genetic anomaly.

Sushanta K Sahoo, Renu Madan, Debajyoti Chatterjee, Mayur Parkhi, Anurodh Kumar

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In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Sushanta K SahooDepartment of Neurosurgery, PGIMER Chandigarh, Sector 12, Chandigarh, 160012, India. drsushantsahoo@gmail.com.
Renu MadanDepartment of Radiotherapy, PGIMER, Chandigarh, India.
Debajyoti ChatterjeeDepartment of Pathology, PGIMER, Chandigarh, India.
Mayur ParkhiDepartment of Pathology, PGIMER, Chandigarh, India.
Anurodh KumarDepartment of Neurosurgery, PGIMER Chandigarh, Sector 12, Chandigarh, 160012, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMedulloblastoma is the commonest embryonal brain tumor in children. Their association with other neuroepithelial brain tumors is less known. Here we discuss a pediatric patient who developed esthesioneuroblastoma 2 years after treatment of medulloblastoma. MATERIALS AND

methodsA 12-year-old male presented with features of raised intracranial hypertension, and radiology showed posterior fossa midline lesion. The tumor was excised, and biopsy revealed medulloblastoma (non-WNT non-SHH type). He received chemoradiation. Two years later he presented with loss of vision, and radiology revealed a sinonasal mass with subfrontal extension. Subtotal resection was done, and biopsy showed blue round cell tumor in favor of esthesioneuroblastoma.

resultParents refused further treatment and the patient died 8months after the second surgery.

conclusionMixed embryonal and neuroepithelial brain tumors are rare. These may have a common genetic abnormality. They have an aggressive course and bear a poor prognosis.

Indexed as

Brain NeoplasmsCerebellar NeoplasmsEsthesioneuroblastoma, OlfactoryMedulloblastomaNose NeoplasmsChildHumansIncidenceMaleNasal CavityBrain tumorEsthesioneuroblastomaMedulloblastomaPediatric patient

Identifiers

PMID34623468

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