Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants

D Taïeb, GB Wanna, M Ahmad… - The Lancet Diabetes & …, 2023 - thelancet.com
Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase
subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head and neck …

Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement

D Taïeb, S Nölting, ND Perrier, M Fassnacht… - Nature Reviews …, 2024 - nature.com
Adult and paediatric patients with pathogenic variants in the gene encoding succinate
dehydrogenase (SDH) subunit B (SDHB) often have locally aggressive, recurrent or …

European association of nuclear medicine practice guideline/society of nuclear medicine and molecular imaging procedure standard 2019 for radionuclide imaging of …

D Taïeb, RJ Hicks, E Hindié, BA Guillet… - European journal of …, 2019 - Springer
Purpose Diverse radionuclide imaging techniques are available for the diagnosis, staging,
and follow-up of phaeochromocytoma and paraganglioma (PPGL). Beyond their ability to …

Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline

JWM Lenders, QY Duh, G Eisenhofer… - The Journal of …, 2014 - academic.oup.com
Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …

New perspectives on pheochromocytoma and paraganglioma: toward a molecular classification

J Crona, D Taïeb, K Pacak - Endocrine reviews, 2017 - academic.oup.com
A molecular biology–based taxonomy has been proposed for pheochromocytoma and
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …

Imaging of pheochromocytoma and paraganglioma

JA Carrasquillo, CC Chen, A Jha… - Journal of Nuclear …, 2021 - jnm.snmjournals.org
Imaging plays a critical role in the management of pheochromocytomas and
paragangliomas and often guides treatment. The discovery of susceptibility genes …

The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma …

H Chen, RS Sippel, MS O'Dorisio, AI Vinik, RV Lloyd… - Pancreas, 2010 - journals.lww.com
Pheochromocytomas, intra-adrenal paraganglioma, and extra-adrenal sympathetic and
parasympathetic paragangliomas are neuroendocrine tumors derived from adrenal …

Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and …

I Janssen, EM Blanchet, K Adams, CC Chen… - Clinical Cancer …, 2015 - aacrjournals.org
Purpose: Patients with succinate dehydrogenase subunit B (SDHB) mutation–related
pheochromocytoma/paraganglioma (PHEO/PGL) are at a higher risk for metastatic disease …

[HTML][HTML] Plasma methoxytyramine: a novel biomarker of metastatic pheochromocytoma and paraganglioma in relation to established risk factors of tumour size …

G Eisenhofer, JWM Lenders, G Siegert… - European journal of …, 2012 - Elsevier
BACKGROUND: There are currently no reliable biomarkers for malignant
pheochromocytomas and paragangliomas (PPGLs). This study examined whether …

[HTML][HTML] Adrenal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up

A Berruti, E Baudin, H Gelderblom, HR Haak… - Annals of oncology, 2012 - Elsevier
Two different primary malignancies can arise from the adrenal gland: the adrenocortical
carcinoma (ACC) from the adrenal cortex and the malignant pheochromocytoma from the …