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GE-Portuguese Journal of Gastroenterology
versão impressa ISSN 2341-4545
Resumo
LEE, Soon Liang; NG, Chiun Yann; SIDHU, Jasminder e AWANG, Asmawiza. A Rare Case of Ectopic Adrenocorticotropic Hormone Secretion from Pancreatic Neuroendocrine Tumour Presenting with Cushing Syndrome. GE Port J Gastroenterol [online]. 2023, vol.30, n.3, pp.66-69. Epub 01-Set-2023. ISSN 2341-4545. https://doi.org/10.1159/000521518.
Ectopic adrenocorticotropic hormone secretion (EAS) from the pancreatic neuroendocrine tumour (PNET) is rare, aggressive, and challenging to treat. We hereby present a rare case of EAS from PNET presenting with Cushing syndrome diagnosed with endoscopic ultrasound-guided fine-needle aspiration cytology. This case highlights the advanced presentation of EAS from PNET with poor clinical correlation of hypercortisolism and the grade of PNET.
Palavras-chave : Adrenocorticotropic hormone; Pancreatic neuroendocrine tumour; Cushing syndrome.