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Article

18F-DOPA PET/CT in the evaluation of hereditary SDH-deficiency paraganglioma-pheochromocytoma syndromes.

Clinical nuclear medicine - 1 Jan 2014

Marzola Maria Cristina, Chondrogiannis Sotirios, Grassetto Gaia, Rampin Lucia, Maffione Anna Margherita, Ferretti Alice, Opocher Giuseppe, Schiavi Francesca, Colletti Patrick M, Rubello Domenico

Abstract excerpt

PURPOSE: This study aims to evaluate the role of F-DOPA PET/CT in staging and follow-up of paraganglioma syndromes succinate dehydrogenase (SDH)-mutation-related patients, comparing F-DOPA PET/CT results with morphological imaging and biochemical results. PATIENTS AND METHODS: We retrospectively studied 10 consecutive patients (3 F, 7 M, mean age 32 yrs), all with a genetically demonstrated SDH mutation (5 SDH-D,...

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Source

Identifiers

PMID: 23856824
DOI: 10.1097/RLU.0b013e31829aface

Genes

SDHD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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