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Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension
JWM. Lenders, MN. Kerstens, L. Amar, A. Prejbisz, M. Robledo, D. Taieb, K. Pacak, J. Crona, T. Zelinka, M. Mannelli, T. Deutschbein, HJLM. Timmers, F. Castinetti, H. Dralle, J. Widimský, AP. Gimenez-Roqueplo, G. Eisenhofer
Language English Country Great Britain
Document type Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't, Review
Grant support
Z99 HD999999
Intramural NIH HHS - United States
ZIA HD008735
Intramural NIH HHS - United States
- MeSH
- Biomedical Research MeSH
- Pheochromocytoma * diagnosis genetics therapy MeSH
- Hypertension * MeSH
- Consensus MeSH
- Humans MeSH
- Adrenal Gland Neoplasms * diagnosis genetics therapy MeSH
- Paraganglioma * diagnosis genetics therapy MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Research Support, N.I.H., Intramural MeSH
- Geographicals
- Europe MeSH
: Phaeochromocytoma and paraganglioma (PPGL) are chromaffin cell tumours that require timely diagnosis because of their potentially serious cardiovascular and sometimes life- threatening sequelae. Tremendous progress in biochemical testing, imaging, genetics and pathophysiological understanding of the tumours has far-reaching implications for physicians dealing with hypertension and more importantly affected patients. Because hypertension is a classical clinical clue for PPGL, physicians involved in hypertension care are those who are often the first to consider this diagnosis. However, there have been profound changes in how PPGLs are discovered; this is often now based on incidental findings of adrenal or other masses during imaging and increasingly during surveillance based on rapidly emerging new hereditary causes of PPGL. We therefore address the relevant genetic causes of PPGLs and outline how genetic testing can be incorporated within clinical care. In addition to conventional imaging (computed tomography, MRI), new functional imaging approaches are evaluated. The novel knowledge of genotype-phenotype relationships, linking distinct genetic causes of disease to clinical behaviour and biochemical phenotype, provides the rationale for patient-tailored strategies for diagnosis, follow-up and surveillance. Most appropriate preoperative evaluation and preparation of patients are reviewed, as is minimally invasive surgery. Finally, we discuss risk factors for developing metastatic disease and how they may facilitate personalised follow-up. Experts from the European Society of Hypertension have prepared this position document that summarizes the current knowledge in epidemiology, genetics, diagnosis, treatment and surveillance of PPGL.
Department of Experimental and Clinical Biomedical Sciences University of Florence Florence Italy
Department of Hypertension Institute of Cardiology Warsaw Poland
Department of Internal Medicine Radboud University Medical Center Nijmegen The Netherlands
Department of Medical Sciences Uppsala University Uppsala Sweden
References provided by Crossref.org
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