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Cushing's syndrome caused by an occult source: difficulties in diagnosis and management

Nature Clinical Practice Endocrinology & Metabolism volume 2, pages 642–647 (2006)Cite this article

A Corrigendum to this article was published on 01 January 2007

Abstract

Background A 24-year-old woman presented with a 12.5 kg weight gain over 6 months (mostly abdominal), hirsutism, acne, ankle edema, polydipsia, nocturia, back pain, pigmentation, poor libido and lightened menses to our hospital in May 1986. She had been treated for the previous 2 years with furosemide and spironolactone for peripheral edema, and had stopped the combined oral contraceptive 2 months previously. She did not take tobacco, recreational drugs or alcohol. Upon physical examination she was grossly Cushingoid with florid clinical manifestations.

Investigations Serum potassium and bicarbonate, circadian rhythm of cortisol, low-dose and high-dose dexamethasone suppression tests, plasma adrenocorticotropic hormone (ACTH), corticotropin releasing-hormone stimulation test, CT scan of the pituitary, plain chest radiology, CT scan of the chest and abdomen, trans-sphenoidal pituitary biopsy and histology, CT scan and MRI of the thorax, MRI of the pituitary, octreotide scintigraphy, gastroscopy, colonoscopy, gut peptides, tumor markers, urine 5-hydroxyl-indole-acetic acid, resection, histology, immunocytochemistry and in situ hybridization.

Diagnosis Occult ectopic ACTH syndrome from a presumed appendiceal neuroendocrine tumor. The tumor was only identified some 20 years from initial presentation.

Management Adrenolytic therapy before bilateral adrenalectomy to cure Cushing's syndrome, glucocorticoid and mineralocorticoid replacement therapy, and then repeated surveillance over 20 years to locate the ectopic source of ACTH. This was finally identified by CT scan and excised at laparotomy.

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Figure 1: Venous phase intravenous and oral contrast enhanced CT scan (LightSpeed Ultra®, GE Healthcare, Waukesha, WI), 5 mm slice, pitch 1.35, showing a tumor (arrow) with a fleck of calcification, typical of a neuroendocrine tumor
Figure 2: Venous phase intravenous and oral contrast enhanced CT scan (LightSpeed Ultra®), 5 mm slice, pitch 1.35, showing the tumor (arrow) depicted in Figure 1 to have been present and smaller, yet overlooked 18 months earlier; however, as the tumor, being attached to the mesoappendix, was potentially mobile the apparent change in size might have been caused by a change in orientation

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Authors and Affiliations

  1. Centre for Endocrinology,

    Ashley B Grossman, Philip Kelly, Andrea Rockall & Tara Balwick

  2. St Bartholomew’s Hospital,

    Ashley B Grossman, Philip Kelly, Andrea Rockall & Tara Balwick

  3. University of London, UK.,

    Ashley B Grossman, Philip Kelly, Andrea Rockall & Tara Balwick

  4. a consultant hepatobiliary surgeon at The Royal London Hospital, London, UK

    Satya Bhattacharya

  5. a reader in pathology at the Division of Cancer Sciences and Molecular Pathology, Pathology Department, Royal Infirmary, Glasgow, UK

    Ann McNicol

Authors
  1. Ashley B Grossman
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Correspondence to Ashley B Grossman.

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The authors declare no competing financial interests.

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Grossman, A., Kelly, P., Rockall, A. et al. Cushing's syndrome caused by an occult source: difficulties in diagnosis and management. Nat Rev Endocrinol 2, 642–647 (2006). https://doi.org/10.1038/ncpendmet0327

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