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Introduction Adrenocortical carcinoma (ACC) is a rare and aggressive cancer that affects both children and adults, having an overall incidence of 1–2 cases/million per year. In most cases, cancer presents with steroid hormone excess ( 1
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Department of Neurosurgery, Technical University Munich (TMU), Munich, Germany
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Introduction Adrenocortical carcinoma (ACC) is a rare yet highly aggressive endocrine malignancy with generally poor prognosis ( 1 ). Treatment options for ACC are scarce, with the only potential curative therapy being complete resection ( 2
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Obesity, Type 2 Diabetes and Immunometabolism Research Group, School of Cardiovascular and Metabolic Medicine & Sciences, Faculty of Life Course Sciences, King’s College London, London, UK
Division of Reproductive Health, Warwick Medical School, University of Warwick, Coventry, UK
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Introduction Adrenocortical carcinoma (ACC) is a rare malignancy of the adrenal cortex with an annual incidence of between 0.5 and 2.0 cases per million ( 1 ). Whilst most cases of ACC are sporadic, typically occurring in the fifth and sixth
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positive histology. The diagnosis of adrenal CS was established by suppressed adrenocorticotrophic hormone (ACTH) levels in the context of hypercortisolaemia and histology in keeping with a cortisol-producing adenoma/adrenocortical carcinoma. Patients
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801 – 812 . ( https://doi.org/10.1210/clinem/dgab749 ) 16 Parmar J Key RE Rainey WE . Development of an adrenocorticotropin-responsive human adrenocortical carcinoma cell line . Journal of Clinical Endocrinology and Metabolism 2008 93 4542
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Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland
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, skin atrophy, or buffalo hump) and those with a serum cortisol level of more than 5 μg/dL in the DST, haemorrhage, infections, adrenal pheochromocytoma, primary hyperaldosteronism, metastases, adrenocortical carcinoma, cysts, history of malignancy or
Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER, Unidad 747), ISCIII, Spain
Department of Endocrinology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
Department of Medicine, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain
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://doi.org/10.1080/23772484.2020.1809421 ) 16 Yeoh P Czuber-Dochan W Aylwin S Sturt J . Lived experience of people with adrenocortical carcinoma and associated adrenal insufficiency . Endocrinology, Diabetes and Metabolism 2022 5 e341. ( https
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, autonomous cortisol secretion; ACC, adrenocortical carcinoma; DST, dexamethasone suppression test; NFAI, nonfunctioning adrenal incidentalomas; PHEO, pheochromocytoma; PA, primary aldosteronism; RyC, Ramón y Cajal Hospital. The SPAIN-ALDO registry
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NCI-H295R (adrenocortical carcinoma) cells increases S1P expression and steroidogenesis ( 32 ). Conversely, sphingolipid intermediates ceramide and sphingosine diminish steroidogenesis, with sphingosine purported to directly attenuate the activity of
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excluded from the study, one due to the finding of adrenocortical carcinoma, two due to nonrepresentative samples, and one due to the patient not having undergone adrenalectomy but postmortem obduction. In addition, 22 samples from a previous prospective