Literature DB >> 24037430

Localization and prediction of malignant potential in recurrent pheochromocytoma/paraganglioma (PCC/PGL) using 18F-FDG PET/CT.

Ahmad Saad Fathinul Fikri1, A Kroiss2, A Z F Ahmad3, H Zanariah4, W F E Lau5, C Uprimny2, E Donnemiller2, D Kendler2, A J Nordin3, I J Virgolini2.   

Abstract

BACKGROUND: To our knowledge, data are lacking on the role of 18F-FDG PET/CT in the localization and prediction of neuroendocrine tumors, in particular the pheochromocytoma/paraganglioma (PCC/PGL) group.
PURPOSE: To evaluate the role of 18F-FDG PET/CT in localizing and predicting the malignant potential of PCC/PGL.
MATERIAL AND METHODS: Twenty-three consecutive patients with a history of PCC/PGL, presenting with symptoms related to catecholamine excess, underwent 18F-FDG PET/CT. Final confirmation of the diagnosis was made using the composite references. PET/CT findings were analyzed on a per-lesion basis and a per-patient basis. Tumor SUVmax was analyzed to predict the dichotomization of patient endpoints for the local disease and metastatic groups.
RESULTS: We investigated 23 patients (10 men, 13 women) with a mean age of 46.43 ± 3.70 years. Serum catecholamine levels were elevated in 82.60% of these patients. There were 136 sites (mean SUVmax: 16.39 ± 3.47) of validated disease recurrence. The overall sensitivities for diagnostic CT, FDG PET, and FDG PET/CT were 86.02%, 87.50%, and 98.59%, respectively. Based on the composite references, 39.10% of patients had local disease. There were significant differences in the SUVmax distribution between the local disease and metastatic groups; a significant correlation was noted when a SUVmax cut-off was set at 9.2 (P<0.05).
CONCLUSION: In recurrent PCC/PGL, diagnostic 18F-FDG PET/CT is a superior tool in the localization of recurrent tumors. Tumor SUVmax is a potentially useful predictor of malignant tumor potential. © The Foundation Acta Radiologica 2013 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.

Entities:  

Keywords:  18F-FDG PET/CT; SUVmax; malignant potential; neuroendocrine; pheochromocytoma/paraganglioma; predictor; recurrence

Mesh:

Substances:

Year:  2013        PMID: 24037430     DOI: 10.1177/0284185113504330

Source DB:  PubMed          Journal:  Acta Radiol        ISSN: 0284-1851            Impact factor:   1.990


  5 in total

Review 1.  Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment.

Authors:  Victoria L Martucci; Karel Pacak
Journal:  Curr Probl Cancer       Date:  2014-01-15       Impact factor: 3.187

2.  Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors.

Authors:  Bruna Babic; Dhaval Patel; Rachel Aufforth; Yasmine Assadipour; Samira M Sadowski; Martha Quezado; Naris Nilubol; Tamara Prodanov; Karel Pacak; Electron Kebebew
Journal:  Surgery       Date:  2016-11-16       Impact factor: 3.982

3.  Renal hilar paraganglioma: A case report.

Authors:  Zeinab Ali Abou Yehia; Rashid Khalid Sayyid; Ali Ahmad Haydar
Journal:  World J Radiol       Date:  2014-01-28

4.  Imaging characteristics of nodal metastases in paraganglioma, ameloblastoma and olfactory neuroblastoma: case reports and literature review.

Authors:  Smita Deb; Tim Anton Iseli; Timothy Wong; Pramit M Phal
Journal:  BJR Case Rep       Date:  2016-07-28

Review 5.  Progress in the diagnosis and treatment of paraganglioma.

Authors:  Ben Wang; Jian Qiu
Journal:  Transl Cancer Res       Date:  2019-11       Impact factor: 1.241

  5 in total

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