A rare cause of Cushing's syndrome: an ACTH-secreting phaeochromocytoma

Lars Folkestad, Marianne Skovsager Andersen, Anne Lerberg Nielsen, Dorte Glintborg

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Excess glucocorticoid levels cause Cushing's syndrome (CS) and may be due to pituitary, adrenal or ectopic tumours. Adrenocorticotropic hormone (ACTH) levels are useful in identifying adrenal tumours. In rare cases, ACTH-producing phaeochromocytomas are the cause of CS. We present two cases of ACTH-secreting phaeochromocytoma as the underlying cause of CS. In both cases, female patients presented with the classical clinical signs of CS and an adrenal mass. High ACTH levels raised the suspicion of an ACTH-secreting phaeochromocytoma. The diagnosis was confirmed by urinary catecholamine levels and positive fluorine-18-L-dihydroxyphenylalanine (18F-DOPA) positron emission tomography (PET) CT (Case 1) and fluorodeoxyglucose PET-CT (Case 2). Both patients were treated with an α-blocker prior to surgical intervention. The two cases underline the importance of thorough diagnostic workup in patients with CS. An ACTH-secreting phaeochromocytoma should be checked for in patients with an adrenal mass and elevated ACTH levels.

Original languageEnglish
JournalBMJ Case Reports
Volume2014
ISSN1757-790X
DOIs
Publication statusPublished - 8. Oct 2014

Fingerprint

Dive into the research topics of 'A rare cause of Cushing's syndrome: an ACTH-secreting phaeochromocytoma'. Together they form a unique fingerprint.

Cite this