ReviewNature reviews. Endocrinology2024
International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents.
Erratum issuedAbstract readReviewConsensus Statement
In one paragraph
Review in Nature reviews. Endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.
0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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.
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.
Who cites it
31 citing papers in PubMed.
- Safety and dosimetry of [European journal of nuclear medicine and molecular imaging · 2025Trial
- Catecholamine metabolism revisited: from neurochemistry to integrative physiology and pathophysiology.Physiological reviews · 2026Review
- Pediatric Pheochromocytoma With Rapid Cyclic Blood Pressure Fluctuations: A Case Report.Clinical case reports · 2026Article
- Genotype-dependent [European journal of nuclear medicine and molecular imaging · 2026Article
- Genetic testing in pituitary adenomas: a Pituitary Society International Consensus Statement.Nature reviews. Endocrinology · 2026Review
- The germline landscape of pituitary adenomas: established and emerging predisposition genes.The Journal of clinical endocrinology and metabolism · 2026Review
- Pheochromocytoma multisystem crisis presenting with abdominal pain in an adolescent: a case report.BMC pediatrics · 2026Article
- Genetics of familial acromegaly and pituitary gigantism.The Journal of clinical endocrinology and metabolism · 2026Review
- Pheochromocytomas and Paragangliomas.Endocrinology and metabolism clinics of North America · 2026Review
- Article
- Determinants of false-positive plasma free metanephrines and methoxytyramine: the role of medications and chronic disease.Endocrine-related cancer · 2026Review
- Pediatric non-rhabdomyosarcoma bladder tumors (NRBTs): a 20-year retrospective longitudinal cohort study at a tertiary referral center.Translational andrology and urology · 2026Article
- Preoperative Adrenal Artery Embolization in a Pediatric Patient with Bilateral Pheochromocytomas: A Case Report.Cureus · 2026Article
- Artificial Intelligence and Machine Learning in Pediatric Endocrine Tumors: Opportunities, Pitfalls, and a Roadmap for Trustworthy Clinical Translation.Biomedicines · 2026Review
- A contemporary overview of multiple endocrine neoplasia syndromes: MEN syndromes 1-5 and beyond.Endocrine oncology (Bristol, England) · 2026Review
- Peptide Receptor Radionucleotide Therapy for Unresectable Paediatric Head and Neck Paraganglioma in Aotearoa New Zealand.Case reports in otolaryngology · 2026Article
- Biochemical Diagnosis of Phaeochromocytoma and Paraganglioma in Children and Adolescents: A Retrospective Cohort Study.Clinical endocrinology · 2025Article
- Quantitative [EJNMMI reports · 2025Article
- Update on Systemic Therapies for Metastatic/Unresectable Pheochromocytomas and Paragangliomas and Future Directions.Cancers · 2025Review
- Adrenal causes of endocrine hypertension in childhood or adolescence.Journal of endocrinological investigation · 2025Review
Corrections and comments
- Erratum issued
- Erratum issued
Authors and funding
40 authors.
Ruth T CaseyDepartment of Medical Genetics, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge, UK. rc674@cam.ac.uk.ORCID http://orcid.org/0000-0003-4058-3135
Emile HendriksDepartment of Paediatric Diabetes and Endocrinology, Cambridge Cancer Centre and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Cheri DealEndocrine and Diabetes Service, CHU Sainte-Justine and University of Montreal, Montreal, Québec, Canada.
Steven G WaguespackDepartment of Endocrine Neoplasia and Hormonal Disorders, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Verena WiegeringUniversity Children's Hospital, Department of Paediatric Hematology, Oncology and Stem Cell Transplantation, University of Würzburg, Würzburg, Germany.
Antje RedlichPaediatric Oncology Department, Otto von Guericke University Children's Hospital, Magdeburg, Germany.ORCID http://orcid.org/0000-0002-1732-1869
Scott AkkerSt Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
Rathi PrasadCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, UK.
Martin FassnachtDepartment of Medicine, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.ORCID http://orcid.org/0000-0001-6170-6398
Roderick Clifton-BlighDepartment of Diabetes and Endocrinology, Royal North Shore Hospital, Sydney, New South Wales, Australia.ORCID http://orcid.org/0000-0002-1545-0368
Laurence AmarUniversité de Paris, Paris, France.ORCID http://orcid.org/0000-0003-3942-4276
Stefan BornsteinDepartment of Medicine III, University Hospital Carl Gustav Carus, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-5211-2536
Letizia CanuDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Evangelia CharmandariDivision of Endocrinology, Metabolism and Diabetes, First Department of Paediatrics, National and Kapodistrian University of Athens Medical School, 'Aghia Sophia' Children's Hospital, Athens, Greece.
Alexandra ChrisoulidouUnit of Endocrinology, Theagenio Hospital, Thessaloniki, Greece.
Maria Currás FreixesHereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Institute of Health Carlos III (ISCIII), Madrid, Spain.
Ronald de KrijgerPrincess Maxima Center for Paediatric Oncology, Utrecht, Netherlands.
Luisa de SanctisDepartment of Public Health and Paediatric Sciences, University of Turin, Turin, Italy.
Antonio FojoDivision of Hematology/Oncology, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Amol J GhiaDepartment of Radiation Oncology, University Hospital of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Angela HuebnerDepartment of Paediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Vasilis KosmoliaptsisDepartment of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge, UK.
Michaela KuhlenPaediatrics and Adolescent Medicine, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Marco RaffaelliU.O.C. Chirurgia Endocrina e Metabolica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-1259-2491
Charlotte Lussey-LepoutreService de médecine nucléaire, Inserm U970, Sorbonne université, Groupe hospitalier Pitié-Salpétrière, Paris, France.
Stephen D MarksDepartment of Paediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust and NIHR GOSH Biomedical Research Centre, University College London Great Ormond Street Institute of Child Health, London, UK.
Naris NilubolSurgical Oncology Program, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Mirko Parasiliti-CaprinoEndocrinology, Diabetes and Metabolism, Department of Medical Sciences, University of Turin, Corso Dogliotti, Turin, Italy.
Henri H J L M TimmersDepartment of Internal Medicine, Radboud University Medical Centre, Nijmegen, Netherlands.
Anna Lena ZietlowClinical Child and Adolescent Psychology, Institute of Clinical Psychology and Psychotherapy, Department of Psychology, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-7278-5711
Mercedes RobledoHereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Institute of Health Carlos III (ISCIII), Madrid, Spain.ORCID http://orcid.org/0000-0001-6256-5902
Anne-Paule Gimenez-RoqueploUniversité Paris Cité, PARCC, INSERM, Paris, France.ORCID http://orcid.org/0000-0002-4816-670X
Ashley B GrossmanOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-1176-6186
David TaïebDepartment of Nuclear Medicine, La Timone University Hospital, CERIMED, Aix-Marseille University, Marseille, France.
Eamonn R MaherDepartment of Medical Genetics, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge, UK.
Jacques W M LendersDepartment of Internal Medicine, Radboud University Medical Centre, Nijmegen, Netherlands.
Graeme EisenhoferDepartment of Medicine III, University Hospital Carl Gustav Carus, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Camilo JimenezDepartment of Endocrine Neoplasia and Hormonal Disorders, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Karel PacakSection on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Rockville, MD, USA.ORCID http://orcid.org/0000-0002-3541-3767
Christina PamporakiDepartment of Medicine III, University Hospital Carl Gustav Carus, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany. Christina.Pamporaki@ukdd.de.ORCID http://orcid.org/0000-0003-0772-1604
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumours that arise not only in adulthood but also in childhood and adolescence. Up to 70-80% of childhood PPGL are hereditary, accounting for a higher incidence of metastatic and/or multifocal PPGL in paediatric patients than in adult patients. Key differences in the tumour biology and management, together with rare disease incidence and therapeutic challenges in paediatric compared with adult patients, mandate close expert cross-disciplinary teamwork. Teams should ideally include adult and paediatric endocrinologists, oncologists, cardiologists, surgeons, geneticists, pathologists, radiologists, clinical psychologists and nuclear medicine physicians. Provision of an international Consensus Statement should improve care and outcomes for children and adolescents with these tumours.
Indexed as
Adrenal Gland NeoplasmsParagangliomaPheochromocytomaAdolescentChildHumans
Identifiers
PMID
39147856What 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.