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M. F. Nijhoff, O. M. Derkers, L. J. Vleming, J. W. A. Smit, J. A. Romijn and A. M. Pereira, “ACTH-Producing Pheocromocytoma: Clinical Considerations and Concise Review of the Literature,” European Journal of Internal Medicine, Vol. 20, No. 7, 2009, pp. 682-685. doi:10.1016/j.ejim.2009.08.002

has been cited by the following article:

• TITLE: Severe Ectopic Cushing’s Syndrome Due to ACTH-Secreting Pheochromocytoma

  AUTHORS: Aurelio Negro, Enrica Manicardi, Chiara Grasselli, Massimiliano Babini, Rosaria Santi, Valeria Pugni, Lucia Spaggiari, Elena Tagliavini

  KEYWORDS: Cushing’s Syndrome; Pheochromocytoma; Apparent Excess of Mineralocorticoid Syndrome

  JOURNAL NAME: International Journal of Clinical Medicine, Vol.4 No.4, April 30, 2013

  ABSTRACT: We report a new case of ectopic Cushing’s syndrome caused by an ACTH-producing pheochromocytoma. A 55-year-old woman presented with a history of severe proximal muscle weakness, polyuria, progressive virilization, anxiety, dyspnea on exercise, difficult to treat hypertension, and type 2 diabetes mellitus since 4 months. The laboratory data demonstrated ACTH-dependent hypercortisolism. The abdominal computed tomography scan showed a 30 mm well-defined mass in the left adrenal gland suggestive for pheochromocytoma. The adrenal veins were sampled, with intraprocedural cortisol measurement, to dosing selective ACTH and cathecolamines. The results established clearly the left adrenal gland as the source of ACTH overproduction. A left sided adrenalectomy was performed with subsequent resolution of Cushing’s syndrome. The patient was discharged in good clinical condition.