The first International Symposium on Phaeochromocytoma in 2005 was followed by considerable progress in the field, largely owing to the many collaborations and networks stimulated by that and subsequent meetings. The rich hereditary background of phaeochromocytomas has since provided for strong interdisciplinary links of genetics with personalized diagnostics, imaging and therapeutic interventions.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Hemorrhage in pheochromocytoma surgery: evaluation of preoperative risk factors
Endocrine Open Access 15 April 2022
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$29.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Dahia, P. L. M. Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity. Nat. Rev. Cancer 14, 108–119 (2014).
Eisenhofer, G., Klink, B., Richter, S., Lenders, J. W. M. & Robledo, M. Metabologenomics of phaeochromocytoma and paraganglioma: an integrated approach for personalised biochemical and genetic testing. Clin. Biochem. Rev. 38, 69–100 (2017).
Taïeb, D., Jha, A., Treglia, G. & Pacak, K. Molecular imaging and radionuclide therapy of pheochromocytoma and paraganglioma in the era of genomic characterization of disease subgroups. Endocr. Relat. Cancer 26, R627–R652 (2019).
Nölting, S., Grossman, A. & Pacak, K. Metastatic phaeochromocytoma: spinning towards more promising treatment options. Exp. Clin. Endocrinol. Diabetes 127, 117–128 (2019).
Pacak, K. et al. Pheochromocytoma: recommendations for clinical practice from the First International Symposium. Nat. Clin. Pract. Endocrinol. Metab. 3, 92–102 (2007).
Fishbein, L. et al. Comprehensive molecular characterization of pheochromocytoma and paraganglioma. Cancer Cell 31, 181–193 (2017).
Crona, J., Taïeb, D. & Pacak, K. New perspectives on pheochromocytoma and paraganglioma: toward a molecular classification. Endocr. Rev. 38, 489–515 (2017).
Job, S. et al. Telomerase activation and ATRX mutations are independent risk factors for metastatic pheochromocytoma and paraganglioma. Clin. Cancer Res. 25, 760–770 (2019).
Taïeb, D. et al. European Association of Nuclear Medicine Practice Guideline/Society of Nuclear Medicine and Molecular Imaging Procedure Standard 2019 for radionuclide imaging of phaeochromocytoma and paraganglioma. Eur. J. Nucl. Med. Mol. Imaging 46, 2112–2137 (2019).
Lenders, J. W. M. et al. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J. Clin. Endocrinol. Metab. 99, 1915–1942 (2014).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Related links
International Collaboration on Cancer Reporting: www.iccr-cancer.org/datasets
Rights and permissions
About this article
Cite this article
Pacak, K., Eisenhofer, G. & Tischler, A.S. Phaeochromocytoma — advances through science, collaboration and spreading the word. Nat Rev Endocrinol 16, 621–622 (2020). https://doi.org/10.1038/s41574-020-00413-w
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41574-020-00413-w
This article is cited by
-
Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas
Endocrine Pathology (2022)
-
Hemorrhage in pheochromocytoma surgery: evaluation of preoperative risk factors
Endocrine (2022)
-
What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?
Endocrine Pathology (2021)
-
Nature Reviews Endocrinology at 15
Nature Reviews Endocrinology (2020)