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Korean Journal of Medicine ; : 67-71, 2014.
Article in Korean | WPRIM | ID: wpr-69091

ABSTRACT

Neuroendocrine tumors of the gallbladder are rare, and typically found incidentally after a cholecystectomy. Few data are available on adrenocorticotrophic hormone (ACTH)-producing neuroendocrine tumors originating specifically from the gallbladder. We experienced the case of a patient with a gallbladder mass who presented with Cushing's syndrome, who was subsequently diagnosed as an ACTH-producing neuroendocrine carcinoma of the gallbladder. Despite being rare, hormone-producing neuroendocrine tumors should be part of the differential diagnosis in patients with Cushing's syndrome.


Subject(s)
Humans , ACTH Syndrome, Ectopic , Adrenocorticotropic Hormone , Carcinoma, Neuroendocrine , Cholecystectomy , Cushing Syndrome , Diagnosis, Differential , Gallbladder , Neuroendocrine Tumors
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