Author:
Thorner Michael O.,Martin William H.,Ragan Gary E.,MacLeod Robert M.,Feldman Philip S.,Bruni Carlo,Williamson Brian R. J.,Orth David N.
Abstract
Abstract.
A patient with a thymic carcinoid tumour causing ectopic ACTH syndrome is presented. The case illustrates the rapid development of the clinical and laboratory findings often associated with ectopic secretion of ACTH, including severe proximal myopathy, emotional lability, and hypokalaemic alkalosis. Interpretation of conventional tests of pituitary-adrenal function was complicated by intermittent secretion of ACTH by the tumour. The results of selective venous sampling for ACTH ruled out pituitary ACTH hypersecretion and were suggestive of a thymic source; computerized tomography of the chest localized the tumour. In vivo and in vitro investigations confirmed excessive ACTH production by the tumour, and surgical resection plus radiotherapy has resulted in resolution of the syndrome.
The diagnostic problems created by intermittent secretion of ACTH by these tumours and the pre-operative and post-operative medical management of these patients are discussed.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
36 articles.
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