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Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK
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Introduction Primary tumours of adenohypophyseal cells recently suggested to be redefined as pituitary neuroendocrine tumours (PitNETs) can rarely occur in association with paraganglioma (PGL) or phaeochromocytoma. These tumours may develop in
Département de Médecine Génomique des Tumeurs et des Cancers, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France
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Biomedical Research Networking Centre on Rare Diseases (CIBERER), Institute of Health Carlos III, Madrid, Spain
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Mays Cancer Center at UTHSCSA, San Antonio, Texas, USA
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entities. The fifth series of the WHO classification of endocrine and neuroendocrine tumors published in 2022 describes clearly PCC as part of the PGL family of tumors by defining PCC as a neuroendocrine neoplasm that originates from chromaffin cells of the
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Department of Endocrinology, Royal North Shore Hospital, St Leonards, Australia
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has an advantage for non-polar, volatile compounds. MALDI as a third ionization approach most often is applied in imaging MS. PPGL and catecholamine metabolism Non-epithelial neuroendocrine neoplasms originating from neural crest-derived cells