4.3 Article

The Ectopic Adrenocorticotropic Hormone Syndrome Rarely Easy, Always Challenging

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W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.ecl.2018.01.005

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Ectopic; Cushing's; ACTH; Carcinoid; Neuroendocrine tumor; Small cell lung cancer

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Despite modern imaging techniques, differentiating ectopic adrenocorticotropic hormone (ACTH) syndrome from pituitary-dependent Cushing's syndrome, Cushing's disease, is especially difficult when well-differentiated carcinoids are the source of ACTH secretion, particularly pulmonary carcinoid tumors. ACTH-secreting pulmonary carcinoids, such as the corticotroph adenomas causing Cushing's disease, are often small and difficult to detect, and patients present with a gradual onset of the classical signs and symptoms of Cushing's syndrome, indistinguishable from the presentation of Cushing's disease. Hence, the differential diagnosis relies on a combination of clinical assessment, dynamic biochemical tests, inferior petrosal sinus sampling, and multimodal imaging, each with its own caveats and pitfalls.

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