TY - JOUR
T1 - European clinical guidance for the management of adrenal and extra-adrenal paraganglioma in children and adolescents
T2 - a consensus by the EXPeRT group
AU - Kuhlen, Michaela
AU - Virgone, Calogero
AU - Rigaud, Charlotte
AU - Irtan, Sabine
AU - Casey, Ruth
AU - Pamporaki, Christina
AU - Kunstreich, Marina
AU - Lopez-Almara, Ricardo
AU - Ben-Ami, Tal
AU - Bien, Ewa
AU - Krawczyk, Malgorzata A.
AU - Mazic Cesen, Maja
AU - Ferrari, Andrea
AU - Bisogno, Gianni
AU - Reguerre, Yves
AU - Abele, Michael
AU - Schneider, Dominik T.
AU - Fuchs, Jörg
AU - Brecht, Ines B.
AU - Timmermann, Beate
AU - De Krijger, Ronald R.
AU - Lapa, Constantin
AU - Redlich, Antje
AU - Orbach, Daniel
N1 - © The Author(s) 2025. Published by Oxford University Press on behalf of European Society of Endocrinology.
PY - 2025/11/26
Y1 - 2025/11/26
N2 - 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.
AB - 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.
KW - EXPeRT
KW - clinical guidance
KW - paraganglioma
KW - pediatric PGL
KW - pheochromocytoma
KW - rare tumors
KW - Paraganglioma/therapy
KW - Humans
KW - Paraganglioma, Extra-Adrenal/therapy
KW - Consensus
KW - Europe/epidemiology
KW - Adolescent
KW - Practice Guidelines as Topic/standards
KW - Child
KW - Adrenal Gland Neoplasms/therapy
UR - https://www.scopus.com/pages/publications/105024017724
UR - https://www.mendeley.com/catalogue/6131de28-6863-391d-aa43-ddf5b864b5be/
U2 - 10.1093/ejendo/lvaf239
DO - 10.1093/ejendo/lvaf239
M3 - Article
C2 - 41261973
AN - SCOPUS:105024017724
SN - 0804-4643
VL - 193
SP - G13-G126
JO - European journal of endocrinology
JF - European journal of endocrinology
IS - 6
ER -