Related Experiment Video
Updated: Apr 7, 2026

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
Ectopic Adrenocorticotropic Hormone Syndrome Secondary to Pulmonary Neuroendocrine Tumor: Medical Stabilization
Muhammed Kizilgul1,2, Ilitch Diaz-Gutierrez3, Diana Oramas Mogrovejo4
1University of Minnesota, Division of Diabetes, Endocrinology & Metabolism, Department of Medicine, Minneapolis, Minnesota.
Background:
Ectopic adrenocorticotropic hormone (ACTH) syndrome accounts for 15% to 20% of Cushing syndrome cases with unique diagnostic challenges. Tumor localization remains difficult, with approximately 20% of cases having occult sources despite extensive imaging. This report describes a patient whose initially occult tumor was successfully localized through serial imaging enabled by medical stabilization, resulting in curative surgical resection.
Case Presentation:
Thirty-nine-year-old woman presented with progressive weight gain, new-onset hypertension, hypokalemia, proximal muscle weakness, and cushingoid features. Laboratory evaluation demonstrated severe hypercortisolism with markedly elevated ACTH levels, and inferior petrosal sinus sampling confirmed the diagnosis of ectopic ACTH syndrome. Despite comprehensive imaging-including cross-sectional studies, gallium-68 (68Ga)-DOTA-D-Phe1,Tyr3-octreotate positron emission tomography/computed tomography, and FDG PET/CT-the ectopic source remained elusive. Medical therapy with ketoconazole and metyrapone achieved rapid biochemical control. An 8 mm lingular pulmonary nodule, non-avid on both DOTATATE and FDG PET but identified on the CT portion of FDG PET/CT, was surgically resected, resulting in complete biochemical cure.
Discussion:
This case highlights medical stabilization's critical role when tumor localization is initially unsuccessful, enabling serial anatomic imaging that identified an 8 mm pulmonary carcinoid initially obscured by atelectasis and nonavid on functional imaging. Small, well-differentiated neuroendocrine tumors can cause severe hypercortisolism, yet remain undetectable on DOTATATE and FDG PET.
Conclusion:
This case demonstrates that medical stabilization achieves rapid biochemical control, providing time for serial anatomic imaging to localize occult ectopic ACTH sources. A small pulmonary carcinoid initially obscured by atelectasis and non:avid on functional imaging was identified through repeat CT comparison, enabling curative resection and avoiding bilateral adrenalectomy.
Related Concept Videos
Adrenal Gland Disorders
Adrenal insufficiency, characterized by insufficient cortisol and aldosterone production, leads to conditions like Addison's disease. This disorder, affecting the adrenal cortex, exhibits symptoms such as skin bronzing, dehydration, low blood pressure, fatigue, and weight loss. Congenital adrenal hyperplasia, a genetic ailment causing...
Hypothalamic-Pituitary Axis
Pulmonary Hypertension: Classification and Pathogenesis
There are various classifications for PH, each relating to different underlying causes and also...
Sympathetic Pathways: Collateral Ganglia and Adrenal Medulla
Collateral Ganglia
Sympathetic preganglionic axons reach the collateral ganglia along the route of splanchnic nerves. These nerves bypass the sympathetic trunk and communicate with sympathetic postganglionic neurons housed in the prevertebral ganglia. These ganglia supply the organs of the abdominopelvic cavity.
The greater splanchnic nerve, formed by the...
Hormones of the Adrenal Glands
The adrenal cortex, a powerhouse of hormone synthesis, generates over two dozen corticosteroid hormones. The zona glomerulosa produces mineralocorticoids, exemplified by aldosterone, influencing the electrolyte composition of body fluids. The synthesis of glucocorticoids such as cortisol and...

