Cushing’s Syndrome Due to Ectopic Corticotropin Secretion: Twenty Years’ Experience at the National Institutes of Health

• Published in: The journal of clinical endocrinology and metabolism 2005-08, Vol.90 (8), p.4955-4962
• Main Authors: Ilias, Ioannis, Torpy, David J., Pacak, Karel, Mullen, Nancy, Wesley, Robert A., Nieman, Lynnette K.
• Format: Article
• Language: English
• Subjects: Adolescent; Adrenals. Adrenal axis. Renin-angiotensin system (diseases); Adrenocorticotropic Hormone - secretion; Adult; Aged; Biological and medical sciences; Carcinoid Tumor - complications; Carcinoid Tumor - mortality; Carcinoid Tumor - secretion; Child; Cushing Syndrome - diagnosis; Cushing Syndrome - etiology; Cushing Syndrome - mortality; Cushing Syndrome - therapy; Endocrinopathies; Female; Follow-Up Studies; Fundamental and applied biological sciences. Psychology; Humans; Lung Neoplasms - complications; Lung Neoplasms - mortality; Lung Neoplasms - secretion; Male; Medical sciences; Middle Aged; National Institutes of Health (U.S.); Non tumoral diseases. Target tissue resistance. Benign neoplasms; Prognosis; Retrospective Studies; Survival Rate; United States; Vertebrates: endocrinology
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.2004-2527

Context: Ectopic ACTH secretion (EAS) is difficult to diagnose and treat. We present our experience with EAS from 1983 to 2004. Setting: The study was performed at a tertiary care clinical research center. Patients: Ninety patients, aged 8–72 yr, including 48 females were included in the study. Interventions and Outcome Measures: Tests included 8 mg dexamethasone suppression, CRH stimulation, inferior petrosal sinus sampling (IPSS), computed tomography, octreotide scan, magnetic resonance imaging, and/or venous sampling. Therapies, pathological examinations, and survival were noted. Results: Eighty-six to 94% of patients did not respond to CRH or dexamethasone suppression, whereas 66 of 67 had negative IPSS. To control hypercortisolism, 62 patients received medical treatment, and 33 had bilateral adrenalectomy. Imaging localized tumors in 67 of 90 patients. Surgery confirmed an ACTH-secreting tumor in 59 of 66 patients and cured 65%. Nonthymic carcinoids took longest to localize. Deaths included three of 35 with pulmonary carcinoid, two of five with thymic carcinoid, four of six with gastrinoma, two of 13 with neuroendocrine tumor, two of two with medullary thyroid cancer, one of five with pheochromocytoma, three of three with small-cell lung cancer, and two of 17 with occult tumor. Patients with other carcinoids and ethesioneuroblastoma are alive. Conclusions: IPSS best identifies EAS. Initial failed localization is common and suggests pulmonary carcinoid. Although only 47% achieved cure, survival is good except in patients with small-cell lung cancer, medullary thyroid cancer, and gastrinoma.