Faten Cherchir, Sawsen Essayeh, Sabrine Mekni, Wafa Ben Hilel, Faten Gargouri, Karima Khiari, Ibtissam Ben Nacef, Imène Rojbi
{"title":"胰腺神经内分泌肿瘤致副肿瘤库欣综合征1例","authors":"Faten Cherchir, Sawsen Essayeh, Sabrine Mekni, Wafa Ben Hilel, Faten Gargouri, Karima Khiari, Ibtissam Ben Nacef, Imène Rojbi","doi":"10.21037/apc-23-5","DOIUrl":null,"url":null,"abstract":"Background: Endogenous Cushing syndrome results from uncontrolled overproduction of cortisol. Paraneoplastic Cushing syndrome (PCS) is an uncommon etiology of endogenous hypercortisolism caused generally by bronchial and thymic adrenocorticotropic hormone (ACTH)-producing tumors. Pancreatic neuroendocrine tumors (NETs) have been reported in only few cases.","PeriodicalId":8372,"journal":{"name":"Annals of Pancreatic Cancer","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Paraneoplastic Cushing syndrome caused by a pancreatic neuroendocrine tumor: a case report\",\"authors\":\"Faten Cherchir, Sawsen Essayeh, Sabrine Mekni, Wafa Ben Hilel, Faten Gargouri, Karima Khiari, Ibtissam Ben Nacef, Imène Rojbi\",\"doi\":\"10.21037/apc-23-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Endogenous Cushing syndrome results from uncontrolled overproduction of cortisol. Paraneoplastic Cushing syndrome (PCS) is an uncommon etiology of endogenous hypercortisolism caused generally by bronchial and thymic adrenocorticotropic hormone (ACTH)-producing tumors. Pancreatic neuroendocrine tumors (NETs) have been reported in only few cases.\",\"PeriodicalId\":8372,\"journal\":{\"name\":\"Annals of Pancreatic Cancer\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Pancreatic Cancer\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21037/apc-23-5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Pancreatic Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21037/apc-23-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Paraneoplastic Cushing syndrome caused by a pancreatic neuroendocrine tumor: a case report
Background: Endogenous Cushing syndrome results from uncontrolled overproduction of cortisol. Paraneoplastic Cushing syndrome (PCS) is an uncommon etiology of endogenous hypercortisolism caused generally by bronchial and thymic adrenocorticotropic hormone (ACTH)-producing tumors. Pancreatic neuroendocrine tumors (NETs) have been reported in only few cases.