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Insulinome associé à une insuffisance corticotrope et un hypogonadisme hypergondadotrope: à propos d’une observation

Pancreatic insulinoma is a rare, often benign, neuroendocrine tumor which may give rise to life-threatening consequences due to hypoglycemia-related accidents. Adrenal deficiency can also cause hypoglycemia. We report the case of a 68-year old patient hospitalized for recurrent hypoglycaemia. Tests...

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Detalles Bibliográficos
Autores principales: Hadjkacem, Faten, Kalthoum, Mahdi, Ghorbel, Dorra, Ammar, Mouna, Elleuch, Mouna, Charfi, Nadia, Mnif, Mouna, Abid, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859031/
https://www.ncbi.nlm.nih.gov/pubmed/31762900
http://dx.doi.org/10.11604/pamj.2019.34.32.14865
Descripción
Sumario:Pancreatic insulinoma is a rare, often benign, neuroendocrine tumor which may give rise to life-threatening consequences due to hypoglycemia-related accidents. Adrenal deficiency can also cause hypoglycemia. We report the case of a 68-year old patient hospitalized for recurrent hypoglycaemia. Tests were performed that showed endogenous hyperinsulinism, adrenocorticotropin deficiency and hypergonadotropic hypogonadism. The patient received hydrocortisone without improvement. Five years later topography showed insulinoma. This study highlights the clinical, biological, radiological and therapeutic features of insulinoma as well as laboratory test results and shows that insulinoma can cause adrenocorticotropic deficiency and peripheral hypogonadism.