Department of Medicine, Mater Dei Hospital, Msida, Malta
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Department of Medicine, Mater Dei Hospital, Msida, Malta
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Introduction Craniopharyngiomas are rare but challenging tumours. Despite being a serious condition, population-based epidemiological data on craniopharyngiomas are limited in other studies ( Bunin et al. 1998 , Haupt et al . 2006
Garvan Institute of Medical Research, Sydney, NSW, Australia
St Vincent’s Clinical School, University of New South Wales, Sydney, NSW, Australia
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Faculty of Medicine, the University of Queensland, Brisbane, QLD, Australia
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Garvan Institute of Medical Research, Sydney, NSW, Australia
St Vincent’s Clinical School, University of New South Wales, Sydney, NSW, Australia
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sella region such as craniopharyngiomas or meningiomas. The authors have chosen not to discuss the proposed nomenclature change from ‘pituitary adenoma’ to ‘PitNET’, as described in the WHO 2022 classification, as this is the subject of significant
Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Belgrade, Belgrade, Serbia
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Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Belgrade, Belgrade, Serbia
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, papillary craniopharyngioma and is identified in corticotroph adenomas ( Gualtieri et al. 2021 ). Mutations in BRAF have a high occurrence rate in different cancers. So the same underlying genetic driver has different unknown roles in different cell types