Evidence map›Paper›PMID 42333331›Full record

ArticleCureus2026

Glioblastoma Arising in an Immature Teratoma: A Rare Somatic Malignancy in a Germ Cell Tumor.

Sagarika Pahwa, Sunipa Ghosh Pradhan, Soumendra Mishra, Sudipta Roy, Sandipan Chowdhuri

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. 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

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

5 authors.

Sagarika PahwaPathology, Saroj Gupta Cancer Centre and Research Institute, Kolkata, IND.
Sunipa Ghosh PradhanPathology, Saroj Gupta Cancer Centre and Research Institute, Kolkata, IND.
Soumendra MishraPathology, Saroj Gupta Cancer Centre and Research Institute, Kolkata, IND.
Sudipta RoyPathology, Saroj Gupta Cancer Centre and Research Institute, Kolkata, IND.
Sandipan ChowdhuriSurgical Oncology, Saroj Gupta Cancer Centre and Research Institute, Kolkata, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mature cystic teratomas constitute the most common ovarian neoplasm occurring in childhood. All the components present in mature cystic teratoma are, by definition, mature. Immature teratomas, on the other hand, are malignant, and they constitute a mixture of embryonal and adult tissues derived from all three germ layers. Commonly, the main component is neuroepithelium. The treatment of immature teratoma is surgery and multidrug chemotherapy for grade 2 and 3 tumours. Sometimes only mature components persist in metastatic sites, which may continue to grow (growing teratoma syndrome) following chemotherapy. Emergence of benign or malignant neoplasm with somatic-type features is an uncommon event in mature cystic teratomas. The most common malignant change is squamous cell carcinoma, followed by carcinoid tumour and adenocarcinoma. Other types include melanomas, sarcomas of various types, carcinosarcomas, glioblastoma, etc. Glioblastomas are among extremely rare somatic malignancies arising from mature or immature teratomas. Their etiology is not well understood, and it is still a matter of research whether they share the same genetic alteration as the tumours occurring in the central nervous system. We present a rare case of glioblastoma arising in an immature teratoma in a young female in her early 20s.

Indexed as

germ cell tumour (gct)glioblastomahigh-grade immature ovarian teratomarare cancers of female genital tractsomatic malignancy

Identifiers

PMID42333331
PMCPMC13283303

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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.