Disseminated Nocardiosis in Ectopic Adrenocorticotropic Hormone Syndrome: A Case ReportChrysanthidis, Theofilos MD*; Yavropoulou, Maria P. MD†; Metallidis, Simeon MD*; Mpakaimi, Isidora MD*; Zempekakis, Pantelis MD*; Yovos, John G. MD†; Nikolaidis, Pavlos MD*The Endocrinologist: November/December 2010 - Volume 20 - Issue 6 - pp 286-287 doi: 10.1097/TEN.0b013e3181fcff16 Case Report Buy Abstract Author Information This report describes a case of Cushing syndrome due to ectopic adrenocorticotropic hormone (ACTH) secretion, complicated with disseminated nocardiosis. A 52-year-old postmenopausal woman presented with acute onset of hirsutism and easy bruisability associated with fatigue and generalized weakness, predominantly involving the proximal musculature of the extremities. Laboratory evaluation revealed high cortisol and ACTH levels, with negative pituitary magnetic resonance imaging (MRI). A 2-day high-dose dexamethasone suppression test (8 mg/d) was indicative of ectopic ACTH secretion. During the course of the disease, the patient developed disseminated nocardiosis that involved the left lung, skin, and central nervous system and was treated accordingly. Despite ketokonazole treatment, cortisol levels remained high and a bilateral adrenalectomy was planned but not performed because the patient died approximately 2 months after initial admission. From the Divisions of *Infectious Diseases, and †Endocrinology and Metabolism, 1st Department of Internal Medicine, AHEPA University Hospital, Thessaloniki, Greece. Reprints: Maria P. Yavropoulou, MD, Division of Endocrinology and Metabolism, 1st Department of Internal Medicine, AHEPA University Hospital, 1 S. Kyriakidi street 54636, Thessaloniki, Greece. E-mail: email@example.com. © 2010 Lippincott Williams & Wilkins, Inc.