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European clinical guidance for the management of adrenal and extra-adrenal paraganglioma in children and adolescents: a consensus by the EXPeRT group

  • Michaela Kuhlen
  • , Calogero Virgone
  • , Charlotte Rigaud
  • , Sabine Irtan
  • , Ruth Casey
  • , Christina Pamporaki
  • , Marina Kunstreich
  • , Ricardo Lopez-Almara
  • , Tal Ben-Ami
  • , Ewa Bien
  • , Malgorzata A. Krawczyk
  • , Maja Mazic Cesen
  • , Andrea Ferrari
  • , Gianni Bisogno
  • , Yves Reguerre
  • , Michael Abele
  • , Dominik T. Schneider
  • , Jörg Fuchs
  • , Ines B. Brecht
  • , Beate Timmermann
  • Ronald R. De Krijger, Constantin Lapa, Antje Redlich, Daniel Orbach

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Background Adrenal (formerly termed pheochromocytomas) and extra-adrenal paragangliomas (PGLs) in children and adolescents are rare neuroendocrine tumors characterized by unique biological behavior, a strong hereditary component, and significant risk of recurrence and metastatic progression. Their management requires specialized, multidisciplinary care. Objective This guidance provides harmonized, evidence-graded recommendations for the diagnosis, treatment, and follow-up of pediatric PGL, developed by the European Cooperative Study Group for Pediatric Rare Tumors (EXPeRT) as part of the European Standard Clinical Practice (ESCP) initiative. Methods Recommendations were formulated through structured consensus by a multidisciplinary panel of experts in pediatric oncology, endocrinology, surgery, nuclear medicine, genetics, and pathology, based on literature review, existing international guidelines, and integration of external adviser feedback. Levels of evidence and grades of recommendation follow a simplified GRADE (Grading of Recommendations, Assessment, Development and Evaluation) system. Recommendations Diagnosis should be based on plasma-free metanephrine and normetanephrine as first-line test, complemented by appropriate anatomical and functional imaging guided by biochemical phenotype and genotype. Germline genetic testing is recommended. Tumor resection remains the mainstay of curative treatment, with cortical-sparing adrenalectomy advised in bilateral hereditary cases (except SDHB). Management of metastatic disease should be individualized, incorporating radionuclide therapy, systemic treatments, focal therapies, and palliative care as appropriate. Lifelong surveillance is essential, tailored to genotype and disease characteristics. Conclusion This European clinical guidance offers practical recommendations to support multidisciplinary management of pediatric PGL within European healthcare systems, complementing existing international consensus statements and supporting harmonization of care.

Original languageEnglish
Pages (from-to)G13-G126
JournalEuropean journal of endocrinology
Volume193
Issue number6
DOIs
Publication statusPublished - 26 Nov 2025
Externally publishedYes

Keywords

  • EXPeRT
  • clinical guidance
  • paraganglioma
  • pediatric PGL
  • pheochromocytoma
  • rare tumors
  • Paraganglioma/therapy
  • Humans
  • Paraganglioma, Extra-Adrenal/therapy
  • Consensus
  • Europe/epidemiology
  • Adolescent
  • Practice Guidelines as Topic/standards
  • Child
  • Adrenal Gland Neoplasms/therapy

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