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Ioannis Ilias, Anju Sahdev, Rodney H Reznek, Ashley B Grossman, and Karel Pacak
Umasuthan Srirangalingam, Bernard Khoo, Lisa Walker, Fiona MacDonald, Robert H Skelly, Emad George, David Spooner, Linda B Johnston, John P Monson, Ashley B Grossman, W M Drake, Scott A Akker, Patrick J Pollard, Nick Plowman, Norbert Avril, Daniel M Berney, Jacky M Burrin, Rodney H Reznek, V K Ajith Kumar, Eamonn R Maher, and Shern L Chew
noted in 5/16 (31%) SDHB mutation carriers at a median of 4 years (range 1.5–25) after the initial tumour. To date, no member of the VHL group has developed evidence of malignant disease. Subgroup analysis A subgroup analysis was carried out to
Francien H van Nederveen, Esther Korpershoek, Ronald J deLeeuw, Albert A Verhofstad, Jacques W Lenders, Winand N M Dinjens, Wan L Lam, and Ronald R de Krijger
Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma . Genes, Chromosomes & Cancer 5 399 – 403 . Thompson LD 2002 Pheochromocytoma of the adrenal gland scaled score (PASS) to separate benign from malignant neoplasms: a
Alexandru Saveanu, Mihaela Muresan, Catherine De Micco, David Taieb, Anne-Laure Germanetti, Frederic Sebag, Jean-François Henry, Laurent Brunaud, Alain Enjalbert, Georges Weryha, and Anne Barlier
, extraadrenal, and malignant pheochromocytomas . Journal of Clinical Endocrinology and Metabolism 80 1837 – 1844 doi:10.1210/jc.80.6.1837 . van Essen M Krenning EP Kooij PP Bakker WH Feelders RA de Herder WW Wolbers JG Kwekkeboom DJ 2006
Frederic Castinetti, Jeffrey Moley, Lois Mulligan, and Steven G Waguespack
Introduction While the first clinical association between pheochromocytoma and medullary thyroid carcinoma (MTC) was described in 1961 by Sipple ( Sipple 1961 ), it was only 5 years later that the first description of oral mucosal neuromas in
Andreas Machens, Steffen Hauptmann, and Henning Dralle
–15 years, the molecular foundations of this heritable tumor syndrome of medullary thyroid cancer, pheochromocytoma, and parathyroid hyperplasia and adenoma have emerged: missense mutations – and exceptionally in-frame insertions and deletions – in the
Katharina Wang, Ina Schütze, Sebastian Gulde, Nicole Bechmann, Susan Richter, Jana Helm, Michael Lauseker, Julian Maurer, Astrid Reul, Gerald Spoettl, Barbara Klink, Doreen William, Thomas Knösel, Juliane Friemel, Michel Bihl, Achim Weber, Maria Fankhauser, Laura Schober, Diana Vetter, Martina Broglie Däppen, Christian G Ziegler, Martin Ullrich, Jens Pietzsch, Stefan R Bornstein, Christian Lottspeich, Matthias Kroiss, Martin Fassnacht, Vera Ursula Julia Wenter, Roland Ladurner, Constanze Hantel, Martin Reincke, Graeme Eisenhofer, Ashley B Grossman, Karel Pacak, Felix Beuschlein, Christoph J Auernhammer, Natalia S Pellegata, and Svenja Nölting
International Randomized Study in malignant progressive pheochromocytoma and paragangliomas (FIRSTMAPPP): an academic double-blind trial investigating sunitinib . Annals of Oncology 32 S621 – S625 . doi:10.1016/annonc/annonc700. Bayley JP Devilee P 2020
Elena Rapizzi, Rossella Fucci, Elisa Giannoni, Letizia Canu, Susan Richter, Paolo Cirri, and Massimo Mannelli
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant pheochromocytomas . Cancer Research 63 5615 – 5621 . Goffrini P Ercolino T Panizza E Giachè V Cavone L Chiarugi A Dima V Ferrero I Mannelli M 2009
Sophie Moog, Charlotte Lussey-Lepoutre, and Judith Favier
Silvera S Bertherat J Bertagna X Schlumberger M Jeunemaitre X Gimenez-Roqueplo AP 2007 Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas . Journal of Clinical
Tobias Else
and malignant pheochromocytomas of the organs of Zuckerkandl . Annals of Internal Medicine 52 126 – 133 . ( doi:10.7326/0003-4819-52-1-126 ). Cornog JL Wilkinson JH Arvan DA Freed RM Sellers AM Barker C 1970 Extra
