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Andrea Weckman Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Fabio Rotondo Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Antonio Di Ieva Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Luis V Syro Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Henriett Butz Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Michael D Cusimano Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Kalman Kovacs Division of Neurosurgery, Division of Pathology, Department of Neurosurgery, Department of Surgery

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Autophagy is an important intracellular process involving the degradation of cytoplasmic components. It is involved in both physiological and pathological conditions, including cancer. The role of autophagy in cancer is described as a ‘double-edged sword,’ a term that reflects its known participation in tumor suppression, tumor survival and tumor cell proliferation. Available research regarding autophagy in endocrine cancer supports this concept. Autophagy shows promise as a novel therapeutic target in different types of endocrine cancer, inhibiting or increasing treatment efficacy in a context- and cell-type-dependent manner. At present, however, there is very little research concerning autophagy in endocrine tumors. No research was reported connecting autophagy to some of the tumors of the endocrine glands such as the pancreas and ovary. This review aims to elucidate the roles of autophagy in different types of endocrine cancer and highlight the need for increased research in the field.

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-15-0042
Volume/Issue:
Volume 22: Issue 4
Free access
Jan Willem B de Groot Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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Bart Rikhof Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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Jaap van Doorn Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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Henk J G Bilo Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands
Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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Maarten A Alleman Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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Aafke H Honkoop Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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Winette T A van der Graaf Department of Internal Medicine,, Department of Metabolic and Endocrine Diseases,, Department of Internal Medicine,, Department of Medical Oncology,, Isala Klinieken, Dr van Heesweg 2, 8025 AB Zwolle, The Netherlands

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This review focuses on the tumour types and symptoms associated with non-islet cell tumour-induced hypoglycaemia (NICTH) as well as the pathogenesis, diagnosis and treatment of this rare paraneoplastic phenomenon. In addition, we report two illustrative cases of patients suffering from NICTH caused by a solid fibrous tumour and a haemangiopericytoma respectively. In the first case, NICTH resolved following complete resection of the tumour, but in the second case the patient needed long-term treatment aimed at controlling hypoglycaemia because of non-resectable metastases. Many tumour types have been associated with NICTH. The crucial event in the development of NICTH seems to be overexpression of the IGF-II gene by the tumour. NICTH is characterised by recurrent fasting hypoglycaemia and is associated with the secretion of incompletely processed precursors of IGF-II (‘big’-IGF-II) by the tumour. This induces dramatic secondary changes in the circulating levels of insulin, GH, IGF-I and IGF-binding proteins, resulting in an insulin-like hypoglycaemic activity of ‘big’-IGF-II.

Article Type:
Research Article
DOI:
https://doi.org/10.1677/ERC-07-0161
Volume/Issue:
Volume 14: Issue 4
Free access
Pedro Iglesias Department of Endocrinology, Hospital Universitario Puerta de Hierro Majadahonda, Majadahonda, Madrid, Spain
Instituto de Investigación Sanitaria Puerta de Hierro Segovia de Arana (IDIPHISA), Majadahonda, Madrid, Spain

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Inmaculada Peiró Clinical Nutrition Unit, Catalan Institute of Oncology, L’Hospitalet de Llobregat, Barcelona, Spain
Unit of Nutrition and Cancer-IDIBELL, L’Hospitalet de Llobregat, Barcelona, Spain

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Betina Biagetti Department of Endocrinology, Universitari Vall d’Hebron, Barcelona, Spain

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Miguel Paja-Fano Department of Endocrinology, Hospital Universitario de Basurto, Bilbao, Spain

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Diana Ariadel Cobo Department of Endocrinology, Complejo Asistencial Universitario de León, León, Spain

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Carlos García Gómez Department of Endocrinology, Hospital Universitario Puerta de Hierro Majadahonda, Majadahonda, Madrid, Spain

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Manuel Mateu-Salat Department of Endocrinology, Hospital Sant Pau, Hospital Sant Pau, Barcelona, Spain
Department of Medicine/Endocrinology, IIB-Sant Pau, Research Center for Pituitary Diseases, Barcelona, Spain

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Idoia Genua Department of Endocrinology, Hospital Sant Pau, Hospital Sant Pau, Barcelona, Spain
Department of Medicine/Endocrinology, IIB-Sant Pau, Research Center for Pituitary Diseases, Barcelona, Spain

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Margarita Majem Department of Oncology, Hospital Sant Pau, Barcelona, Spain

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Mariona Riudavets Department of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France

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Javier Gavira Department of Oncology, Hospital Sant Pau, Barcelona, Spain

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Cristina Lamas Department of Endocrinology, Hospital General Universitario de Albacete, Albacete, Spain

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Antía Fernández Pombo Department of Endocrinology, Hospital Clínico Universitario de Santiago, Santiago de Compostela, A Coruña, Spain

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Fernando Guerrero-Pérez Department of Endocrinology, Hospital Universitari de Bellvitge, L’Hospitalet de Llobregat, Barcelona, Spain

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Carles Villabona Department of Endocrinology, Hospital Universitari de Bellvitge, L’Hospitalet de Llobregat, Barcelona, Spain

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José Manuel Cabezas Agrícola Department of Endocrinology, Hospital Clínico Universitario de Santiago, Santiago de Compostela, A Coruña, Spain

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Susan M Webb Department of Endocrinology, Hospital Sant Pau, Hospital Sant Pau, Barcelona, Spain
Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER, Unidad 747), ISCIII, Universitat Autònoma de Barcelona, Barcelona, Spain

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Juan J Díez Department of Endocrinology, Hospital Universitario Puerta de Hierro Majadahonda, Majadahonda, Madrid, Spain
Instituto de Investigación Sanitaria Puerta de Hierro Segovia de Arana (IDIPHISA), Majadahonda, Madrid, Spain
Department of Medicine, Universidad Autónoma de Madrid, Madrid, Spain

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hypertension, dyslipidemia, and type 2 diabetes mellitus, respectively. Nine (24.3%) patients showed a previous endocrine disease (multinodular goiter ( n  = 4), silent thyroiditis ( n  = 2), primary hypothyroidism ( n  = 1), hyperthyroidism ( n  = 1), and

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-21-0228
Volume/Issue:
Volume 28: Issue 12
Restricted access
S L Asa Department of Pathology and Endocrine Oncology Site Group, Princess Margaret Cancer Centre, University Health Network, Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada

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O Casar-Borota Department of Pathology, Uppsala University Hospital, Uppsala, Sweden

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P Chanson Service of Endocrinology and Reproductive Diseases, Bicêtre Hospital, Paris, France

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E Delgrange Department of Medicine, University of Louvain, Mont-sur-Meuse, Belgium

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P Earls Department of Anatomical Pathology, St Vincent’s Hospital, Sydney, Australia

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S Ezzat Department of Medicine and Endocrine Oncology Site Group, Princess Margaret Cancer Centre, University Health Network and University of Toronto, Toronto, Ontario, Canada

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A Grossman Department of Endocrinology, University of Oxford, Oxford, UK

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H Ikeda Research Institute for Pituitary Disease, Southern Tohoku General Hospital, Fukushima, Japan

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N Inoshita Department of Pathology, Toranomon Hospital, Tokyo, Japan

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N Karavitaki Department of Endocrinology, Queen Elizabeth Hospital, University of Birmingham, Birmingham, UK

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M Korbonits Division of Endocrinology, Queen Mary Hospital, Barts and the London School of Medicine, London, UK

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E R Laws Jr Department of Neurosurgery, Harvard Medical School, Brigham & Women’s Hospital, Boston, Massachusetts, USA

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M B Lopes Departments of Pathology and Neurological Surgery, University of Virginia, Charlottesville, Virginia, USA

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N Maartens Department of Neurosurgery, Royal Melbourne Hospital, The University of Melbourne, Melbourne, Australia

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I E McCutcheon Department of Neurosurgery, UT MD Anderson Cancer Center, Houston, Texas, USA

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O Mete Department of Pathology and Endocrine Oncology Site Group, Princess Margaret Cancer Centre, University Health Network, Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada

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H Nishioka Department of Neurosurgery, Toranomon Hospital, Tokyo, Japan

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G Raverot Department of Endocrinology, Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France

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F Roncaroli Department of Neuropathology, Imperial College, London, UK

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W Saeger Institute of Neuropathology of the University of Hamburg, Hamburg, Germany

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L V Syro Department of Neurosurgery, Hospital Pablo Tobon Uribe, Medellin, Colombia

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A Vasiljevic Department of Pathology, Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France

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C Villa Department of Pathology, Hôpital Foch, Suresnes, France

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A Wierinckx INSERM U1052, Cancer Research Center of Lyon, University of Lyon, Lyon, France

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J Trouillas Faculty of Medicine Lyon-Est, University of Lyon, Lyon, France

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and the attendees of 14th Meeting of the International Pituitary Pathology Club, Annecy, France, November 2016
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encourage tumor registries to capture data on these tumors, thereby assisting efforts to clarify clinical and pathological features that can appropriately guide patient management. Pituitary neuroendocrine tumors are not simply endocrine diseases, but should

Article Type:
Article Commentary
DOI:
https://doi.org/10.1530/ERC-17-0004
Volume/Issue:
Volume 24: Issue 4
Free access
Francesca Branzoli Paris Brain Institute - Institut du Cerveau (ICM), Center for Neuroimaging Research (CENIR), Paris, France
Sorbonne University, UMR S 1127, Inserm U 1127, CNRS UMR 7225, ICM, Paris, France

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Betty Salgues Sorbonne University, nuclear medicine department, Pitié-Salpêtrière Hospital, Assistance -Publique Hôpitaux de Paris, Paris, France
Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France

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Małgorzata Marjańska Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota, Minneapolis, Minnesota, USA

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Marie Laloi-Michelin Endocrinology department, Lariboisière Hospital, Assistance -Publique Hôpitaux de Paris, Paris, France

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Philippe Herman ENT unit, Lariboisière Hospital, Assistance -Publique Hôpitaux de Paris, Paris-Cité University, INSERM U1141, Paris, France

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Lauriane Le Collen Inserm/CNRS UMR 1283/8199, Pasteur Institute of Lille, EGID, University of Lille, Lille, France
Department of Endocrinology Diabetology, University Hospital Center of Reims, Reims, France
Department of Genetic, University Hospital Center of Reims, Reims, France

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Brigitte Delemer Department of Endocrinology Diabetology, University Hospital Center of Reims, Reims, France
CRESTIC EA 3804, University of Reims Champagne Ardenne, UFR Sciences Exactes et Naturelles, Moulin de La Housse, BP 1039, Reims, France

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Julien Riancho AP-HP, Hôpital Européen Georges Pompidou, Hypertension Unit, and Reference centre for rare adrenal diseases, Paris, France

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Emmanuelle Kuhn Pituitary Unit, Pitié-Salpêtrière Hospital APHP, Sorbonne University, Paris, France

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Christel Jublanc Pituitary Unit, Pitié-Salpêtrière Hospital APHP, Sorbonne University, Paris, France

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Nelly Burnichon Département de médecine génomique des tumeurs et des cancers, AP-HP, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France

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Laurence Amar AP-HP, Hôpital Européen Georges Pompidou, Hypertension Unit, and Reference centre for rare adrenal diseases, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France

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Judith Favier Université Paris Cité, Inserm, PARCC, Paris, France

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Anne-Paule Gimenez-Roqueplo Département de médecine génomique des tumeurs et des cancers, AP-HP, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France

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Alexandre Buffet Département de médecine génomique des tumeurs et des cancers, AP-HP, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France

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Charlotte Lussey-Lepoutre Sorbonne University, nuclear medicine department, Pitié-Salpêtrière Hospital, Assistance -Publique Hôpitaux de Paris, Paris, France
Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France

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history of endocrine disease was referred to an endocrine unit for a right cervical mass evolving for several years. CT scan revealed an intensely enhanced right carotid bifurcation mass with splaying of the internal and external carotid arteries

Article Type:
Research Article
DOI:
https://doi.org/10.1530/ERC-22-0198
Volume/Issue:
Volume 30: Issue 2
Restricted access
Jessica L Geiger Division of Hematology/Oncology, Department of Internal Medicine, University of Pittsburgh Cancer Institute, Division of Anatomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Pittsburgh Medical Center, Division of Molecular Genomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, 5150 Centre Avenue, 5th Floor, Pittsburgh, Pennsylvania, 15232, USA

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Simion I Chiosea Division of Hematology/Oncology, Department of Internal Medicine, University of Pittsburgh Cancer Institute, Division of Anatomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Pittsburgh Medical Center, Division of Molecular Genomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, 5150 Centre Avenue, 5th Floor, Pittsburgh, Pennsylvania, 15232, USA

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Sue M Challinor Division of Hematology/Oncology, Department of Internal Medicine, University of Pittsburgh Cancer Institute, Division of Anatomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Pittsburgh Medical Center, Division of Molecular Genomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, 5150 Centre Avenue, 5th Floor, Pittsburgh, Pennsylvania, 15232, USA

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Marina N Nikiforova Division of Hematology/Oncology, Department of Internal Medicine, University of Pittsburgh Cancer Institute, Division of Anatomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Pittsburgh Medical Center, Division of Molecular Genomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, 5150 Centre Avenue, 5th Floor, Pittsburgh, Pennsylvania, 15232, USA

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Julie E Bauman Division of Hematology/Oncology, Department of Internal Medicine, University of Pittsburgh Cancer Institute, Division of Anatomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Pittsburgh Medical Center, Division of Molecular Genomic Pathology, Department of Pathology, University of Pittsburgh Medical Center, 5150 Centre Avenue, 5th Floor, Pittsburgh, Pennsylvania, 15232, USA

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. Journal of Clinical Endocrinology and Metabolism 81 2041 – 2046 . Mulligan LM Ponder BA 1995 Genetic basis of endocrine disease: multiple endocrine neoplasia type 2 . Journal of Clinical Endocrinology and Metabolism 80 1989 – 1995

Article Type:
Editorial
DOI:
https://doi.org/10.1530/ERC-15-0307
Volume/Issue:
Volume 22: Issue 5
Free access
Thibault Bahougne Service d’Endocrinologie et Diabétologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France
Institut des Neurosciences Cellulaires et Intégratives, CNRS (UPR 3212), Strasbourg, France

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Alessio Imperiale Service de Biophysique et de Médecine Nucléaire, Hôpitaux Universitaires de Strasbourg, Strasbourg, France
ICube, UMR 7357 Université de Strasbourg/CNRS et FMTS, Faculté de Medécine, Strasbourg, France

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Gerlinde Averous Département de Pathologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

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Gerard Chabrier Service d’Endocrinologie et Diabétologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

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Nelly Burnichon Département de Génétique, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Descartes, PRES Sorbonne Paris Cité, Faculté de Médecine, Paris, France
INSERM, UMR970, Paris-Centre de Recherche Cardiovasculaire, Paris, France

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Anne Paule Gimenez-Roqueplo Département de Génétique, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Descartes, PRES Sorbonne Paris Cité, Faculté de Médecine, Paris, France
INSERM, UMR970, Paris-Centre de Recherche Cardiovasculaire, Paris, France
Centre Expert National COMETE-Cancer de la surrénale, Paris, France

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Nassim Dali-Youcef Laboratoire de Biochimie et de Biologie Moléculaire, Hôpitaux Universitaires de Strasbourg, Strasbourg, France
Institut de Génétique et Biologie Moléculaire et Cellulaire (IGBMC)/CNRS/INSERM/Université de Strasbourg, Illkirch, France

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Rossella Libe Centre Expert National COMETE-Cancer de la surrénale, Paris, France
Endocrinology Department, Cochin Hospital, Paris, France
Département de Médecine Nucléaire et de Tumeurs Endocrines, Institut Gustave Roussy, Université Paris Sud, Villejuif, France

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Eric Baudin Département de Médecine Nucléaire et de Tumeurs Endocrines, Institut Gustave Roussy, Université Paris Sud, Villejuif, France

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Catherine Roy Service de Radiologie B, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

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Herve Lang Service d’Urologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

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Laurence Kessler Service d’Endocrinologie et Diabétologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

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F Cabanillas M Arfi-Roufe J Berdelou A Moon B Al Ghuzlan A 2014 Therapy of endocrine disease: treatment of malignant pheochromocytoma and paraganglioma . European Journal of Endocrinology 171 R111 – R122 . ( doi:10

Article Type:
Letter
DOI:
https://doi.org/10.1530/ERC-16-0431
Volume/Issue:
Volume 24: Issue 2
Free access
Joanna Grey Association for Multiple Endocrine Neoplasia Disorders (AMEND), Tunbridge Wells, Kent, UK

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Kym Winter Association for Multiple Endocrine Neoplasia Disorders (AMEND), Tunbridge Wells, Kent, UK

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together with its expert medical advisors to provide information resources and support services to families in the UK and elsewhere affected by MEN disorders and related endocrine diseases. References Allen C Vassilev I Kennedy A Rogers A 2016

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-17-0335
Volume/Issue:
Volume 25: Issue 2
Free access
Inga-Lena Nilsson
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Jan Zedenius
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Li Yin
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Anders Ekbom
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primarily on incidence as opposed to mortality or whether the risk may be reduced by normalizing the biochemical disturbances through parathyroid adenectomy (PTX). More insight into these matters is important since pHPT is an endocrine disease that affects

Article Type:
Research Article
DOI:
https://doi.org/10.1677/erc.1.01261
Volume/Issue:
Volume 14: Issue 1
Free access
M Montani
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A M Schmitt
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S Schmid
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T Locher
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P Saremaslani
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P U Heitz
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P Komminoth
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A Perren
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or thyroid tissues were used as non-neoplastic tissue in 20 and 14 patients respectively. No non-neoplastic tissue was available for patient no. 29 (Table 1 ). Blood samples from 80 unrelated Swiss individuals not suffering from endocrine disease were

Article Type:
Research Article
DOI:
https://doi.org/10.1677/erc.1.00996
Volume/Issue:
Volume 12: Issue 4
Free access