Evidence map›Paper›PMID 38336898›Full record

GuidelineNature reviews. Endocrinology2024

Consensus guideline for the diagnosis and management of pituitary adenomas in childhood and adolescence: Part 2, specific diseases.

Márta Korbonits, Joanne C Blair, Anna Boguslawska, John Ayuk, Justin H Davies, Maralyn R Druce, Jane Evanson, Daniel Flanagan, Nigel Glynn, Claire E Higham and 7 more

Open access · bronzeAbstract readPractice GuidelineReview
PubMed Publisher
In one paragraph

Guideline in Nature reviews. Endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
13.6field-weighted citation impact, top 1% of its field
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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Observational
  2. Article
  3. Review
  4. Review
  5. Review
  6. Acromegaly diagnosis.The Journal of clinical endocrinology and metabolism · 2026
    Review
  7. Cushing's disease across the lifespan: a case-based clinical review.Archives of endocrinology and metabolism · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Mammosomatotroph pituitary neuroendocrine tumour in a 7-year-old boy: case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

17 authors at 13 institutions in 2 countries.

Márta KorbonitsCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK. m.korbonits@qmul.ac.uk.ORCID http://orcid.org/0000-0002-4101-9432
Joanne C BlairAlder Hey Children's Hospital, Liverpool, UK.
Anna BoguslawskaDepartment of Endocrinology, Jagiellonian University Medical College, Krakow, Poland.ORCID http://orcid.org/0000-0002-1348-3924
John AyukUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Justin H DaviesUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Maralyn R DruceCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Jane EvansonNeuroradiology, Barts Health NHS Trust, London, UK.
Daniel FlanaganPlymouth Hospitals NHS Trust, Plymouth, UK.
Nigel GlynnCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Claire E HighamThe Christie NHS Foundation Trust, Manchester, UK.
Thomas S JacquesGreat Ormond Street Institute of Child Health, University College London, London, UK.
Saurabh SinhaSheffield Children's and Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Ian SimmonsThe Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Nicky ThorpThe Christie NHS Foundation Trust, Manchester, UK.
Francesca M SwordsNorwich and Norfolk NHS Foundation Trust, Norwich, UK.
Helen L StorrCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID http://orcid.org/0000-0002-9963-1931
Helen A SpoudeasGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Queen Mary University of London · GBThe Christie NHS Foundation Trust · GBBarts Health NHS Trust · GBGreat Ormond Street Hospital · GBJagiellonian University · PLLeeds Teaching Hospitals NHS Trust · GBNorfolk and Suffolk NHS Foundation Trust · GBPlymouth Hospital · GBSheffield Teaching Hospitals NHS Foundation Trust · GBUniversity College London Hospitals NHS Foundation Trust · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pituitary adenomas are rare in children and young people under the age of 19 (hereafter referred to as CYP) but they pose some different diagnostic and management challenges in this age group than in adults. These rare neoplasms can disrupt maturational, visual, intellectual and developmental processes and, in CYP, they tend to have more occult presentation, aggressive behaviour and are more likely to have a genetic basis than in adults. Through standardized AGREE II methodology, literature review and Delphi consensus, a multidisciplinary expert group developed 74 pragmatic management recommendations aimed at optimizing care for CYP in the first-ever comprehensive consensus guideline to cover the care of CYP with pituitary adenoma. Part 2 of this consensus guideline details 57 recommendations for paediatric patients with prolactinomas, Cushing disease, growth hormone excess causing gigantism and acromegaly, clinically non-functioning adenomas, and the rare TSHomas. Compared with adult patients with pituitary adenomas, we highlight that, in the CYP group, there is a greater proportion of functioning tumours, including macroprolactinomas, greater likelihood of underlying genetic disease, more corticotrophinomas in boys aged under 10 years than in girls and difficulty of peri-pubertal diagnosis of growth hormone excess. Collaboration with pituitary specialists caring for adult patients, as part of commissioned and centralized multidisciplinary teams, is key for optimizing management, transition and lifelong care and facilitates the collection of health-related quality of survival outcomes of novel medical, surgical and radiotherapeutic treatments, which are currently largely missing.

Indexed as

AcromegalyAdenomaPituitary NeoplasmsProlactinomaAdolescentAdultAgedChildFemaleHumansMale

Identifiers

PMID38336898
OpenAlexW4391678370

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.