Evidence map›Paper›PMID 40143878›Full record

ArticleCurrent health sciences journal

Unveiling the Uncommon: A Case Series on Rare Germ Cell Tumors.

Asmita Chakrabarti, Shailaja Kumari, Moumita Maiti, Chhanda DAS, Gopinath Barui

Abstract readCase Reports
In one paragraph

Article in Current health sciences journal. 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
–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

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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

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

5 authors.

Asmita ChakrabartiNil Ratan Sircar Medical College and Hospital.
Shailaja KumariNil Ratan Sircar Medical College and Hospital.
Moumita MaitiNil Ratan Sircar Medical College and Hospital.
Chhanda DASNil Ratan Sircar Medical College and Hospital.
Gopinath BaruiNil Ratan Sircar Medical College and Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGerm cell tumors (GCTs) are heterogeneous group of neoplasms that arise from primordial germ cells and can occur in various locations, most commonly in the ovaries and testes but can also be found in extra-gonadal sites like retroperitoneum due to developmental errors. These tumors are relatively rare but clinically significant due to their potential for malignancy and association with developmental anomalies. CASE PRESENTATION: This case series presents four rare and unusual cases of germ cell tumors encountered in both paediatric and adult patients, each with distinctive clinical, radiological, and histopathological features. These cases are unique in their clinical presentation and histomorphological findings, reflecting the diverse spectrum of GCTs across different age groups.

conclusionThese cases underscore the complexity of diagnosis, the role of radiological and histopathological examinations, and the varied management strategies for rare conditions like gonadoblastoma, dysgerminoma, struma ovarii, and fetus-in-fetu.

Indexed as

dysgerminomafetal structurefetus-in-fetuGerm cell tumorsgonadoblastomastruma ovarii

Identifiers

PMID40143878
PMCPMC11936066

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.