A CASE OF PSEUDO-NELSONS SYNDROME - CURE OF ACTH HYPERSECRETION BY REMOVAL OF A BRONCHIAL CARCINOID-TUMOR RESPONSIBLE FOR CUSHINGS-SYNDROME

It may sometimes be difficult to distinguish Cushing’s disease from ectopic ACTH syndrome. A case is described here of a patient with a Cushing’s syndrome and diagnostic difficulties. Initial features were consistent with a Cushing’s disease (in particular metopirone test was positive). Because of relapse of hypercortisolism after mitotane therapy, total adrenalectomy was performed. Thereafter features occurred that evoked Nelson’s syndrome, including high plasma ACTH levels and a pituitary mass syndrome. Pituitary reserve testings by vasopressin or cortico-tropin-releasing factor were positive, although inconstantly, in that plasma ACTH increased. A lung tumor was discovered about 20 yr after the first clinical signs of hypercortisolism. Its removal led to the discovery of a bronchial carcinoid tumor and was followed by normalization of plasma ACTH levels. An analysis of proopiomelanocortin-related peptides was performed postoperatively on the blood drawn before and after the tumor resection and on the tumor; the results of this study would have been contributive to the diagnosis of occult ectopic ACTH tumor. In conclusion this case demonstrates the limitations of the conventional procedures in the diagnosis of the ectopic ACTH syndrome. At contrast the newer biochemical procedures may be very useful in determining the type of hypercortisolism. © 1990, Italian Society of Endocrinology (SIE). All rights reserved.