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Review
. 2019 Jul;51(7):470-482.
doi: 10.1055/a-0926-3618. Epub 2019 Jul 15.

Precision Surgery for Pheochromocytomas and Paragangliomas

Affiliations
Review

Precision Surgery for Pheochromocytomas and Paragangliomas

Douglas Wiseman et al. Horm Metab Res. 2019 Jul.

Abstract

Since Felix Fränkel's account of pheochromocytoma in 1886, great discoveries and vast advancements in the diagnosis, genetics, anatomical and functional imaging techniques, and surgical management of pheochromcytoma and paraganglioma (P-PGL) have been made. The improved insight in the pathophysiology of P-PGL and more accurate detection methods enable physicians to tailor the treatment plan to an individual based on the genetic profile and tumor behavior. This review will cover briefly the clinical features, diagnosis, genetic mutations, and imaging modalities that are used to guide current surgical management of these rare and interesting endocrinopathies.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Computed tomography images a and b and magnetic resonance images c and d of pheochromocytoma a and c and paraganglioma b and d. α: Pheochromocytoma, arrows: Paraganglioma.
Fig. 2
Fig. 2
18F-FDOPA PET/CT a and 68Ga-DOTATATE PET/CT b in patients with SDHB germline mutation and left pheochromocytoma and right neck and intra-abdominal paragangliomas.

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