Cyclic Cushing syndrome due to an ectopic pituitary adenoma.

Nat Clin Pract Endocrinol Metab

Department of Endocrinology, Diabetes and Metabolism, Cleveland Clinic, Cleveland, OH 44195, USA.

Published: March 2009

AI Article Synopsis

  • A 39-year-old man with symptoms of Cushing syndrome, including weight gain, headaches, and bruising, was evaluated for his condition after a history of stable Crohn disease and no glucocorticoid use.
  • Investigations revealed cyclic Cushing syndrome caused by an ectopic pituitary adenoma, confirmed through various hormone tests and imaging techniques.
  • The patient underwent successful transsphenoidal surgery to remove the adenoma, leading to normal adrenal function and resolution of symptoms after 18 months.

Article Abstract

Background: A 39-year-old man was referred to an endocrinology clinic for evaluation of his Cushing syndrome. He had gained 20 kg over 5 years and complained of intermittent headaches and easy bruisability. His medical history included a left foot fracture associated with minimal trauma 2 years earlier, hypertension, and stable Crohn disease with no use of exogenous glucocorticoids for at least 10 years.

Investigations: Measurements of plasma adrenocorticotropic hormone, 24 h urine free cortisol excretion, late-night salivary cortisol, serum cortisol levels before and after corticotropin-releasing hormone administration during a dexamethasone suppression/corticotropin-releasing hormone-stimulation test, pituitary MRI, and inferior petrosal sinus sampling.

Diagnosis: Cyclic Cushing syndrome secondary to an ectopic pituitary adenoma.

Management: The cyclic nature of Cushing syndrome was suggested by the absence of hypercortisolemia during inferior petrosal sinus sampling, and was confirmed by multiple 24 h urine free cortisol measurements. The patient underwent transsphenoidal surgery, during which a 5 mm firm, round, midline sphenoid sinus lesion was identified and resected. In preoperative imaging studies, this lesion had been interpreted as being a mucosal polyp. At microscopic examination, the lesion was found to be a pituitary adenoma, which stained diffusely with antiadrenocorticotropic-hormone antibodies. Explorations of the sella and pituitary did not reveal any abnormalities. Postoperatively, the patient became hypocortisolemic and his cushingoid features resolved. His adrenal function normalized 3 months after surgery. At 18 months, the patient continued to be symptom-free with normal levels of urinary-free cortisol and midnight salivary cortisol.

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Source
http://dx.doi.org/10.1038/ncpendmet1039DOI Listing

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