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Jean-Pierre Bayley and Peter Devilee

attempts to develop models from cultured human tumors. A human paraganglioma cell line was reported in the early 1990s, denoted as EPG1 ( Stuschke et al. 1992 , Stuschke et al. 1995 ), which was derived from a subcutaneous metastasis of a malignant

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Hans K Ghayee, Bas Havekes, Eleonora P M Corssmit, Graeme Eisenhofer, Stephen R Hammes, Zahid Ahmad, Alexander Tessnow, Ivica Lazúrová, Karen T Adams, Antonio T Fojo, Karel Pacak, and Richard J Auchus

Jansen JC van der Mey AG Vriends AH Romijn JA 2007 Malignant paragangliomas associated with mutations in the succinate dehydrogenase D gene . Journal of Clinical Endocrinology and Metabolism 92 1245 – 1248 . van Houtum WH Corssmit EP

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Ruth T Casey, Benjamin G Challis, Alison Marker, Deborah Pitfield, Heok K Cheow, Ashley Shaw, Soo-Mi Park, Helen L Simpson, and Eamonn R Maher

Dear Editor, We have read with great interest the recent article by Tufton and coworkers reporting on the risk of metastasis in patients with paraganglioma (PGL) tumours associated with germline SDHA mutations ( Tufton et al . 2017 ). Herein

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Hartmut P Neumann, William F Young Jr, Tobias Krauss, Jean-Pierre Bayley, Francesca Schiavi, Giuseppe Opocher, Carsten C Boedeker, Amit Tirosh, Frederic Castinetti, Juri Ruf, Dmitry Beltsevich, Martin Walz, Harald-Thomas Groeben, Ernst von Dobschuetz, Oliver Gimm, Nelson Wohllk, Marija Pfeifer, Delmar M Lourenço Jr, Mariola Peczkowska, Attila Patocs, Joanne Ngeow, Özer Makay, Nalini S Shah, Arthur Tischler, Helena Leijon, Gianmaria Pennelli, Karina Villar Gómez de las Heras, Thera P Links, Birke Bausch, and Charis Eng

.1530/ERC-17-0189 ) 10.1530/ERC-17-0189) Castro-Vega LJ Buffet A De Cubas AA Cascon A Menara M Khalifa E Amar L Azriel S Bourdeau I Chabre O , et al . 2014 Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

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Nicola Tufton, Rahul Ghelani, Umasuthan Srirangalingam, Ajith V Kumar, William M Drake, Donato Iacovazzo, Kassiani Skordilis, Daniel Berney, Ma’en Al-Mrayat, Bernard Khoo, and Scott A Akker

associated phenotypes. We suggest that SDHA paraganglioma-related disease is not a low-risk condition as first described. Of our six index cases, two developed metastatic disease and a further one had local vascular invasion. One patient developed multiple

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Jens Waldmann, Volker Fendrich, Julia Holler, Malte Buchholz, Ernst Heinmöller, Peter Langer, Annette Ramaswamy, Birgit Samans, Martin K Walz, Matthias Rothmund, Detlef K Bartsch, and Emily P Slater

Malignant PG 37 20 PGS (SDHD) 15 y HM DM, distant metastases; PC, pheochromocytoma; PG, paraganglioma; n, no; y, yes; PGS, paraganglioma syndrome; LM, liver metastases; LN, lymph node metastases; LG, lung metastases; BN, bone metastases; P, peritoneum; HM

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Camilo Jimenez, Sasan Fazeli, and Alejandro Román-Gonzalez

World Health Organization (WHO), however, recognizes that all pheochromocytomas and paragangliomas have the potential to spread distantly and recommends that the term 'malignant' be avoided in this setting, for example, 'metastatic tumor' is preferred to

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Jenny Welander, Adam Andreasson, Michael Brauckhoff, Martin Bäckdahl, Catharina Larsson, Oliver Gimm, and Peter Söderkvist

Previously reported in pheochromocytoma/paraganglioma ( Comino-Mendez et al . 2013 , Toledo et al . 2013 ). d Previously reported in pheochromocytoma/paraganglioma ( Lorenzo et al . 2013 ). e Malignant according to AFIP criteria ( Lack 2007 ), local

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Erwan Thouënnon, Alice Pierre, Yannick Tanguy, Johann Guillemot, Destiny-Love Manecka, Marlène Guérin, L'houcine Ouafik, Mihaela Muresan, Marc Klein, Jérôme Bertherat, Hervé Lefebvre, Pierre-François Plouin, Laurent Yon, and Youssef Anouar

. Chrisoulidou A Kaltsas G Ilias I Grossman AB 2007 The diagnosis and management of malignant phaeochromocytoma and paraganglioma . Endocrine-Related Cancer 14 569 – 585 . Cleary S Phillips JK Huynh TT Pacak K Elkahloun AG Barb J

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Joakim Crona, Angela Lamarca, Suman Ghosal, Staffan Welin, Britt Skogseid, and Karel Pacak

pheochromocytoma and paraganglioma 2017 malignant pheochromocytoma and paraganglioma: 272 patients over 55 years . Journal of Clinical Endocrinology and Metabolism 102 3296 – 3305 . ( ) Hescot S Curras-Freixes M