Evidence map›Paper›PMID 42238235›Full record

ArticleFrontiers in endocrinology2026

Pubertal dysfunctions in intracranial germ cell tumors.

Cristina Partenope, Sabrina Criscuolo, Fernando Carceller, Assunta Albanese

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

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5 · Who and what money

Authors and funding

4 authors.

Cristina PartenopeDivision of Pediatrics, Department of Health Science University of Piemonte Orientale, Ospedale Maggiore della Carità, Novara, Italy.
Sabrina CriscuoloDepartment of Paediatric Endocrinology, Royal Marsden NHS Foundation Trust, London, United Kingdom.
Fernando CarcellerPaediatric and Adolescent Neuro-Oncology and Drug Development Team, Children and Young People's Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton, United Kingdom.
Assunta AlbaneseDepartment of Paediatric Endocrinology, Royal Marsden NHS Foundation Trust, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pediatric intracranial germ cell tumors (IC-GCTs) are frequently associated with pubertal dysfunctions, either at diagnosis or during follow-up. This study aims to evaluate the prevalence and types of pubertal disorders in a cohort of pediatric patients with IC-GCTs. Methods: We collected clinical, radiological, histopathological, and hormonal data. Pubertal dysfunctions were classified as: (1) pseudo-precocious puberty (PPP, gonadotrophin-independent); (2) central precocious puberty (CPP, gonadotrophin-dependent); (3) hypogonadotrophic hypogonadism (HH). Results: Sixty patients with IC-GCTs (followed-up between 1996 and 2023 at Royal Marsden Hospital, UK) were included (median follow-up 22.9 months). Germinomas represented 70%, teratomas and mixed GCTs 15% each. Tumors were suprasellar (59%), pineal (30%), or bifocal (11%). Treatments included surgery (11%), chemotherapy (78%), and radiotherapy (90%). Pubertal disorders were found in 27 patients (16 males, 11 females). PPP was found in five patients at diagnosis; in three, it resolved with tumor treatment; one required treatment with bicalutamide/anastrozole and one progressed to CPP. Three patients in total developed CPP (one after PPP, one post-PPP with intervening treatment, and one post-cancer treatment completion). HH was diagnosed in 20 cases (mean age 17.5 years in males, 15.1 in females). Two had HH at diagnosis. One female had amenorrhea with polycystic ovary syndrome and responded to combined oral hormonal therapy. No cases of hypergonadotrophic hypogonadism from chemotherapy were observed. Conclusion: Pubertal dysfunctions are common in IC-GCTs, especially with suprasellar involvement. Patterns include PPP, CPP, and HH, which may evolve over time. Long-term specialist endocrine follow-up is essential.

Indexed as

Brain NeoplasmsHypogonadismNeoplasms, Germ Cell and EmbryonalPubertyPuberty, PrecociousAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansMaleadolescentsgerm cell tumorhypogonadotrophic hypogonadismpediatricsprecocious pubertysuprasellar tumor

Identifiers

PMID42238235
PMCPMC13226160

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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.