Evidence map›Paper›PMID 39758788›Full record

ArticleInternational cancer conference journal2025

Intraventricular ganglioneuroblastoma: an uncommon location for a rare tumour in a young adult with review of literature.

Tarang Patel, Garima M Anandani, Virendrakumar Meena

Abstract read
In one paragraph

Article in International cancer conference journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Tarang PatelDepartment of Pathology, All India Institute of Medical Sciences (AIIMS), Rajkot, Gujarat India.ORCID 0000-0001-9901-9147
Garima M AnandaniDepartment of Pathology, All India Institute of Medical Sciences (AIIMS), Rajkot, Gujarat India.
Virendrakumar MeenaDepartment of Radiodiagnosis, Geetanjali Medical College & Hospital, Udaipur, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ganglioneuroblastoma (GNB) is a rare tumour of neuroectodermal origin consisting of a varying proportion of neuroblasts and ganglion cells. GNB arises from sympathoadrenal tissue usually affecting young children. Very few cases of brain GNB have been reported in the literature. To the best of our knowledge, this is the first-ever reported case of GNB at an intraventricular location in young adults. Because of the rarity of the neoplasm, it might be confused with other tumours of intraventricular location both in radiology and histopathology. We report a very rare case, which was surgically operated on and sent for a frozen section followed by a routine report. The final diagnosis was made by Immunohistochemistry (IHC) study. The patient was treated with further radiotherapy.

Indexed as

Embryonal tumoursForamen of MonroGanglioneuroblastomaIntraventricular massRadiotherapySynaptophysinWHO grading

Identifiers

PMID39758788
PMCPMC11695542

What OpenQuestion holds

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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.